Catalent Pharma Solutions jobs in Saint Petersburg, FL - 49 jobs

The Quality Assurance Specialist is responsible for managing and documenting events / discrepancies associated with either product or process as well as managing / writing any investigations that may be a result of those event; processing and investigating customer / consumer product complaints; preparing annual product reviews; and, tracking and trending and follow-up of the CAPA program. Position Summary This position is 100% on-site at the St. Petersburg site. St. Petersburg is our primary soft gel development and manufacturing facility in North America with capacity of 18 billion capsules per year. Within the Catalent network, we offer a broad range of integrated formulation and analytical services to solve difficult development and manufacturing challenges. The Quality Assurance Specialist interacts directly with manufacturing personnel and is responsible for maintaining a high-quality environment within the manufacturing area by overseeing and ensuring compliance with current Good Manufacturing Practices and Standard Operating Procedures through the periodic inspections and monitoring of process controls in all applicable areas of the manufacturing operation. The Role Collaborates with management and supervisory personnel from Operations, Quality Control and Quality Assurance to resolve problems affecting product quality; collaboration includes reacting, investigating and following up with Operations for non-conformance issues and a working jointly towards resolution. Provide guidance and plan of action to the manufacturing floor when production events occur as defined by SOP and lead investigations of non-compliant issues according to procedures as defined by SOPs. Prepare complaint investigation reports and work closely with others on site events to verify scope of investigations, assure root cause analysis and batch impact assessment are adequate, and recommend corrective actions to prevent deviation recurrence; ensure on time closure. May author other types of quality system documents as directed or assigned by QA management. Liaise with customers to ensure customer requirements are satisfied. Facilitate CAPA commitments and Effectiveness Checks, including initiation, tracking, trending, and closure Prepare annual product reports and ensure on time closure. Other duties as assigned. The Candidate Bachelor's Degree in Science or related field required (Chemistry, Microbiology or Biology); A minimum of three years related experience in QA pharmaceutical manufacturing. Prior experience working with investigation writing, including root cause analysis and report writing a must (prior experience with preparing annual product reviews preferred). Working knowledge of cGMPs and/or OSHA regulations required. Ability to work effectively under pressure to meet deadlines. Individual may be required to sit, stand, walk regularly and occasionally lift to 15 pounds; no lifting greater than 44.09 pounds without assistance. Be accessible to manufacturing floor and office staff and to use required office equipment. Specific vision requirements include reading of written documents and frequent use of computer monitor. Why You Should Join Catalent Competitive medical benefits and 401K 152 hours of PTO + 8 Paid Holidays Dynamic, fast-paced work environment Opportunity to work on Continuous Improvement Processes Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

Work Schedule: Rotating 12-hour shift from 7:00AM to 7:00PM EST, operating on a two-week cycle. Week 1 includes Monday, Tuesday, Friday, Saturday, and Sunday; Week 2 includes Wednesday and Thursday. 100% on-site Join Catalent's flagship softgel development and manufacturing facility in North America, located in St. Petersburg, FL, with a capacity of 18 billion capsules per year. This role offers competitive pay, day-one benefits, and career growth in a state-of-the-art, turn-key facility. As an Encapsulation Operator, you will contribute to the manufacturing of pharmaceutical softgels, gaining hands-on experience with multiple technologies and equipment. You'll also collaborate with the on-site Product Development team to support new product innovations. The Role Operates and maintains up to two encapsulation machines, covering up to four during breaks. Manufactures softgels by following batch record instructions and cGMP standards, completing all required documentation. Troubleshoot equipment issues to maintain consistent product quality and minimize downtime. Coordinates with crib mechanics during machine changeovers; performs teardown and setup when utilities are unavailable. Monitors material and gel usage, ensuring components are used within expiration limits and replenishing solvents/lubricants as needed. Maintains a clean work area, performs in-process quality checks, and ensures timely transport of empty receivers. Assembles, handles, and stages tray stacks with manufactured softgels; ensures department supplies are stocked. Handles non-hazardous, hazardous, and DEA-regulated materials and waste in compliance with safety protocols. Other duties as assigned. Qualifications High school diploma or equivalent required Previous manufacturing experience in a GMP-regulated industry preferred Ability to sit, stand, walk, and lift up to 30 lbs regularly during a 12-hour shift; must be able to access the manufacturing floor No lifting over 44.09 lbs without assistance; must be able to push/pull up to 500 kg (approximately 1,100 lbs) Must pass Ishihara Color Vision Screening and achieve 20/30 visual acuity (near and far), with or without corrective lenses Primary workstation is in a high-noise manufacturing area with exposure to industrial chemicals, detergents, flammable materials, and potent drug compounds; annual physical required for handling potent compounds Work schedule may include nights, weekends, and overtime as needed Why You Should Join Catalent Tuition reimbursement to support educational goals 152 hours of PTO plus 8 paid holidays & Medical, dental, and vision benefits effective day one WellHub program to promote physical wellness & Access to Perkspot discounts from over 900 merchants Defined career path with annual performance reviews Inclusive culture with active Employee Resource Groups & Community engagement and green initiatives Strong potential for career growth within a mission-driven organization Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

Work Schedule: Monday - Friday, standard business hours 100% on-site Join Catalent's flagship softgel development and manufacturing facility in St. Petersburg, FL, producing 18 billion capsules annually. This role offers competitive pay, day-one benefits, and career growth in a state-of-the-art facility, where your work directly impacts patient lives. Product Development oversees end-to-end product creation, including benchtop/lab-scale work, feasibility batches, registration/stability batches, and technical support for process validation. The team also supports product investigations, technology transfers to the St. Petersburg, FL facility, and conducts Gap Assessments, Risk Assessments, and implementation of PAT solutions. This role plays a critical part in the timely development of new pharmaceutical products using Softgel formulation and process technologies by executing essential formulation and process activities. The Role Leads and executes experimental studies to generate supporting data and resolve technical issues throughout project lifecycles. Represents Softgel Product Development in internal and customer meetings, clearly communicating technical objectives. Collaborates closely with Analytical Services, Operations, QC, QA, and cross-functional partners to meet all project requirements. Troubleshoots technical challenges, evaluates solution options, and recommends preferred paths forward. Manages workload independently, identifying potential risks to timelines and escalating unresolved issues appropriately. Drives process and procedural improvements that enhance efficiency, safety, and overall quality. Completes technical activities, development reports, and regulatory support documentation while maintaining required training and compliance. Supports and mentors Softgel personnel as needed, ensuring alignment with departmental and company policies. Other duties as assigned. The Candidate BS in scientific field with 5 plus years' experience in lab, 3 in GMP OR MS in scientific field with 3 plus years' experience in GMP lab OR Doctorate in scientific field with 1 plus years' experience in lab. Familiarity with batch processing in a pharmaceutical, cGMP environment. Strong knowledge of cGMP Regulatory requirements for process development, technical transfer, and process changes required with basic to advanced statistical analysis and calculations preferred required. Ability to work effectively under pressure to meet deadlines. Individual may be required to sit, stand, walk regularly and occasionally lift to 15 pounds; no lifting greater than 44.09 pounds without assistance. Vision requirements include ability to differentiate color (Pass the Ishihara Color Vision Screening) and obtain 20/30 acuity in both far and near vision with or without corrective lenses. For Catalent's in-house screening, the acceptable score is to identify at least 4 of 6 numbers in the circles. Why You Should Join Catalent Comprehensive benefits package including medical, dental, and vision coverage effective day one. Generous paid time off - 152 hours of PTO plus 8 paid holidays. Tuition reimbursement and a defined career path with annual performance reviews to support growth. Inclusive, mission-driven culture with active Employee Resource Groups and community engagement. Wellness and lifestyle perks through Perkspot discounts and the WellHub program. Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. St. Petersburg is our primary softgel development and manufacturing facility in North America with a capacity of 18 billion capsules per year. The featured RP Scherer softgel technology is a proven oral drug delivery solution to enhance bioavailability of poorly soluble Rx and OTC drug candidates. Non-gelatin based OptiShell and Vegicaps capsules expand the range of molecules into softgel, ideal for challenging fill formulation. Within the Catalent network, we offer a broad range of integrated formulation and analytical services to solve your most difficult development and manufacturing challenges. The Engineering department involves coordinating, planning, organizing, and managing the engineering and maintenance activities within the Business Unit group to ensure projects and routine tasks are on schedule and meeting expectations. Analyzes and evaluates production problems and processes to develop methods and equipment to improve plant operating efficiencies. This position performs a variety of advanced skilled maintenance on utilities systems in support of the larger manufacturing organization; including but not limited to HVAC repair, painting, water system maintenance, and electrical trades work. This is a full-time on-site hourly position, Monday - Friday 7:00am - 3:30pm Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee. The Role: * Utilizes mechanical and/or electrical skills to perform preventative maintenance, troubleshooting, and repairs to plant facility equipment autonomously; Skilled and capable of completing repairs utilizing various skill sets: Electrical Wiring, brazing, etc. with direct supervision * Ensures that facilities are available for use and consistently maintained in a safe and clean condition * Responsible for more complex and time critical mechanical / electrical equipment rebuilds, repairs and upgrades, manage and escort contractors/vendors * Proposes improvements to processes and methods * Support or own work orders for equipment activities * Ensure detailed inventory of spare parts for all assets are accurately maintained, guarantee parts are on hand for critical equipment * Accurately analyze equipment schematics to identify replacement part numbers and submit purchase requests for emergency spare parts * Acts as a lead, coordinating the work of others - but is not a supervisor. Coach and mentor new technicians * Other duties as assigned The Candidate: * Must have an Associates degree with 4+ years of relevant experience OR * High School diploma and 6+ years of relevant experience * Must possess advanced electrical and/or mechanical skills and education * Technical certificate or higher is preferred * Highly skilled and /or certified in at least one trade is preferred; Advanced machine shop and hand tools experience is preferred * Must be proficient with computers to complete and manage electronic work orders * Must be able to read and understand English-written job instructions and safety requirements * Individual may be required to sit, stand, walk regularly and occasionally lift up to 50 pounds; no lifting greater than 40.09 pounds without assistance. Why you should join Catalent: * Defined career path and annual performance review and feedback process * Diverse, inclusive culture * Positive working environment focusing on continually improving processes to remain innovative * Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives * 152 hours of PTO + 8 paid holidays * Several Employee Resource Groups focusing on D&I * Dynamic, fast-paced work environment * Community engagement and green initiatives * Generous 401K match * Medical, dental and vision benefits * Tuition Reimbursement - Let us help you finish your degree or start a new degree! * WellHub- program to promote overall physical wellness * Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

Senior Contract Specialist This is a full-time salaried position, onsite expectations our of Tampa, FL or Bridgewater, NJ. The Senior Contract Specialist serves as a business partner to our Business Development and Legal organizations. The Senior Contract Specialist will support the development and execution of contracts with new and existing customers ensuring Catalent has strong, profitable contracts with business terms that align with guidelines and represent a win-win for Catalent and our customers. The Senior Contract Specialist is also accountable for organizing internal stakeholders, subject matter experts, Legal and supporting functions across the global Catalent organization to provide for long-term sustainable contracts. The Role: Negotiate contracts in partnership with Business Development, Legal and other functional leads to achieve timely deal closure and growth expectations Mitigates risk through understanding of proposed terms and conditions and develops recommendations for contract language to meet business needs Identify and communicate risk areas throughout the negotiation contract lifecycle and the renewal process. Escalate issues appropriately Drive compliance with Legal, organizational and departmental policies and procedures with adherence to processes and business rules Experience leading contract negotiations and drafting contracts Demonstrated knowledge of contract terms and terminology enabling a comprehensive review and commentary of business contracts Other duties as assigned The Candidate: Bachelor's degree, required Minimum of five years of contracting and negotiating experience, with relevant experience in the Pharmaceutical, Biotechnology or Consumer Health industries Experience leading contract negotiations and drafting contracts Demonstrated knowledge of contract terms and terminology enabling a comprehensive review and commentary of business contracts Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds Pay: New Jersey Posting The anticipated salary range for this position in New Jersey is $100,000 - $130,000, plus bonus, when eligible. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states. Why You Should Join Catalent: Defined career path and annual performance review and feedback process 152 hours of PTO + 8 paid holidays Several Employee Resource Groups focusing on D&I Generous 401K match Medical, dental and vision benefits effective day one of employment Tuition Reimbursement Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

This is a full-time salaried position, based onsite out of our St Petersburg, FL location. The Human Resource Manager is responsible for assisting in the development, implementation and administration of policies and programs for staffing, employee relations, compensation and benefits, employee development and training, organizational development. They will ensure regulatory compliance to meet the business strategies and customer requirements of Oral Technologies, St. Petersburg, Florida within the framework of Catalent's overall corporate philosophy and policies, external laws and regulations. The Role: Develops and directs the establishment and maintenance of policies, procedures, plans and programs dealing with the specific activities of staffing, employee relations, compensation and benefits, employee development and training, organizational development, HR information systems to meet the site's business plan and competitive strategy in a cost-effective manner Ensures alignment of such policies, procedures, plans, programs and budgets with those of Catalent Pharma Solutions Partners with St. Petersburg-based leadership in the organization's strategic planning efforts, providing insight on vital HR concerns and ensuring alignment with overall business objectives Provides counsel to managers and employees on human resources issues, organization structure and development Establishes and maintains an effective and credible relationship with both management and employees; works closely with line management to provide support, planning and problem solving Plans and directs the organization's recruitment, selection and placement of talent with the critical technical and management skills required to ensure the continuity of operations, and leadership bench strength development Other duties as assigned The Candidate: Bachelor's degree required; advance degree, preferred PHR or SPHR certification, preferred Minimum 10 years broad and progressive experience in human resources with 3 years in a management role within organizations with progressive HR systems and processes, preferred Thorough knowledge of payroll principles, required Experience supporting a manufacturing environment (24x7 with 3/2/2 scheduling), preferred Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds Why You Should Join Catalent: Defined career path and annual performance review and feedback process 152 hours of PTO + 8 paid holidays Several Employee Resource Groups focusing on D&I Generous 401K match Medical, dental and vision benefits effective day one of employment Tuition Reimbursement WellHub - program to promote overall physical wellness Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

* Work Schedule: Monday - Friday, standard business hours * 100% on-site Join Catalent's flagship softgel development and manufacturing facility in North America, located in St. Petersburg, FL, with a capacity of 18 billion capsules per year. This role offers competitive pay, day-one benefits, and career growth in a state-of-the-art, turn-key facility. The Senior Project Engineer is responsible for providing technical expertise and management of projects primarily involving the upgrade, installation, troubleshooting, and optimization of process and FAC/UtL equipment and small-scale construction projects. This includes projects supporting new product introduction (NPI), equipment reliability & total productive maintenance (TPM), cost containment, efficiency improvements, and regulatory compliance. The position is responsible to interface with internal stakeholders, suppliers, contractors, and external customers. The Role * Initiate and manage capital projects ($5K-$1M+), including forecasting and milestone expenditure reporting. * Prepare, manage, and communicate project plans for major projects. * Provide engineering technical guidance, generate and document functional requirements and design specifications. * Lead procurement, design approval, construction, installation, and commissioning of new or modified equipment or areas. * Provide technical recommendations for process development, troubleshooting, and maintenance of equipment. * Lead ergonomic and safety assessments, maintain CMMS asset information, and generate equipment SOPs. * Support site Quality (cGMP) and EHS compliance, lead impact assessments, investigations, and CAPAs. * Drive cost-saving and lean initiatives, stay current with new technologies, and mentor or supervise team members. * Other duties as assigned. The Candidate * Bachelor's degree in engineering, physics, mathematics, or other discipline relevant to the project engineering function required. * 8+ years' project engineering experience in a regulated manufacturing industry required, preferably working with pharmaceutical drug products. An advanced technical degree may be substituted for years of experience. * Demonstrated success with large ($250k+) capital project management in area of technical expertise. * Individual may be required to sit, stand, walk regularly and occasionally lift up to 20 pounds, no lifting greater than 44 pounds without assistance. * Specific vision requirements include reading of written documents and use of computer monitor screen frequently. Why You Should Join Catalent * Tuition reimbursement to support educational goals * 152 hours of PTO plus 8 paid holidays & Medical, dental, and vision benefits effective day one * WellHub program to promote physical wellness & Access to Perkspot discounts from over 900 merchants * Inclusive culture with active Employee Resource Groups & Community engagement and green initiatives * Strong potential for career growth within a mission-driven organization Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

* Work Schedule: Monday through Friday, Standard Hours * 100% on-site Join Catalent's flagship softgel development and manufacturing facility in North America, located in St. Petersburg, FL, with a capacity of 18 billion capsules per year. This role offers competitive pay, day-one benefits, and career growth in a state-of-the-art, turn-key facility. The Associate Scientist II, Quality Control role is responsible for independently performing testing and developing assays to identify and characterize raw materials, in-process samples, stability samples, and finished products. The position involves analyzing and documenting data in compliance with cGMP and internal guidelines, communicating results, and supporting procedures, specifications, and test method development. This role is fully on-site in St. Petersburg and includes training colleagues, continuous improvement efforts, and strict adherence to FDA, EPA, OSHA, and safety requirements. The Role * Analysis of finished products, in-process materials, fill moisture, raw materials, and cleaning verification and validation samples according to the assigned specifications, methods and protocols. * Performs analysis of finished products, validation samples, in-process materials and raw materials, moisture testing, Gas, Water and manufacturing environmental sampling and testing according to the effective * Specifications, protocols, Methods and Compendial monograms. * Cultivate and identify bacteria or other microorganisms isolated on selective and non-selective media. * Maintains cultures according to ATCC and departmental Standard Operating Procedures. * Performs identification of microorganisms using techniques such as API, Gram Stain, etc. * Prepares reagents, standards, Medias, etc. needed for analysis. * Interprets and tabulates results of analysis. Records the results in approved notebooks, reports and logbooks. * Other duties as assigned. The Candidate * Requires BS or BA with college course work in related sciences. * Analytical laboratory experience preferred but not required. * Experience with common pharmaceutical laboratory equipment including but not limited to: experience with U.V. spectroscopy experience with IR and AA instrumentation, H.P.L.C. and G.C. instrumentation experience, Autoclave, Vitek, and dissolution testing. * Expertise in wet chemistry techniques such as titrations, extractions, digestions and preparations of test solutions. * Individual may be required to sit, stand, walk regularly and occasionally lift to 15 pounds; no lifting greater than 44.09 pounds without assistance. * Vision requirements include ability to differentiate color (Pass the Ishihara Color Vision Screening) and obtain 20/30 acuity in both far and near vision with or without corrective lenses. For Catalent's in-house screening, the acceptable score is to identify at least 4 of 6 numbers in the circles. Why You Should Join Catalent * Competitive medical benefits and 401K * 152 hours of PTO + 8 Paid Holidays * Dynamic, fast-paced work environment * Opportunity to work on Continuous Improvement Processes Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. This is a full-time salaried position, onsite in St Petersburg, FL. The Controller is responsible for creating an environment of good internal control and accounting practice for the St Pete Softgel facility. The position is key contributor in the establishment and maintenance of disciplined financial process in a fast-paced growth environment. The position is responsible for coordinating all the activities to ensure an accurate, on time month end close and reporting process in accordance with head office deadlines. The incumbent in this role will work in collaboration with the FP&A Manager and Cost Accounting Manager to ensure a good governance environment across the organization. The position will play a key role in the development, attraction and retention of two direct reports. The Controller is also supported by the Shared Services group who provide Accounts Receivable, Accounts Payable and General Accounting support to the facility. The incumbent has a critical role partnering with the offshore Shared Services team to ensure that an effective and efficient service is provided and follow up with any aging balance through the proper reconciliations and agreed action plans. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee. The Role: * Ensure that the Business Unit is compliant with Catalent's financial policies and procedures and generally accepted accounting principles (USGAAP) * Provide overall direction for the month end close process * Ensure that the financial statements clearly reflect the current situation of the business through the correct revenue recognition, the required journal entries and the creation of accruals and provisions to recognize on time the expenses and liabilities that the business could have * Ensure timely and accurate financial results are reported using the GL and Reporting Systems * Responsible for all reporting requirements (JD Edwards, OneStream, monthly/quarterly closing, forecast, budget, etc. * Responsible for the maintenance and integrity of the site transactional systems, including general ledger, accounts receivable, accounts payable, and fixed asset sub ledgers * Ensure that balances in Balance Sheet are accurate and up to date through the definition and establishment of the proper reconciliation methodology for each account based on its nature * Serve as the liaison between the site and both internal and external audit teams * Responsible for satisfying external (Grant Thornton/KPMG, customer requests, Tax audits) and internal audit requirements * Other duties as assigned The Candidate: * Bachelor's degree in Accounting or Finance, required; CPA, preferred * Minimum 10 years of experience in accounting * Experience within a manufacturing environment or pharmaceutical company, preferred * Proficiency level using Excel and Access database, required * Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds * Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience Why You Should Join Catalent: * Defined career path and annual performance review and feedback process * Diverse, inclusive culture * 152 hours of PTO + 8 paid holidays * Several Employee Resource Groups focusing on D&I * Dynamic, fast-paced work environment * Positive working environment focusing on continually improving processes to remain innovative * Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives * Community engagement and green initiatives * Generous 401K match * Medical, dental and vision benefits effective day one of employment * Tuition Reimbursement * WellHub - program to promote overall physical wellness * Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

* Work Schedule: Monday - Friday, standard business hours * 100% on-site Join Catalent's flagship softgel development and manufacturing facility in St. Petersburg, FL, producing 18 billion capsules annually. This role offers competitive pay, day-one benefits, and career growth in a state-of-the-art facility, where your work directly impacts patient lives. Product Development oversees end-to-end product creation, including benchtop/lab-scale work, feasibility batches, registration/stability batches, and technical support for process validation. The team also supports product investigations, technology transfers to the St. Petersburg, FL facility, and conducts Gap Assessments, Risk Assessments, and implementation of PAT solutions. This role plays a critical part in the timely development of new pharmaceutical products using Softgel formulation and process technologies by executing essential formulation and process activities. The Role * Schedule and conduct lab work to ensure timely completion of the required activities. * Perform solubility and compatibility studies. Prepare laboratory fill mixes, air fill capsules. * Prepare gel swatches. Execute drying studies. * Perform fill moisture, water activity, hardness, rheology, burst strength, impact/drop testing, disintegration, dissolution and/or other testing. Perform HPLC analysis. Prepare buffers, mobile phase and dissolution media. * Provide experimental details and record the results in approved notebooks, batch records, reports and logbooks. Prepare samples for animal PK studies. * Provide training to new or existing personnel. * Required to read and execute departmental guidance and SOPs. Comply with Health, Safety and Environmental responsibilities for the position. * Maintain current training records for required procedures. * May be required to work with highly potent compounds, hormones. * Other duties as assigned. The Candidate * Doctorate in Pharmacy/Pharmaceutical Sciences, Chemistry, or related science OR; * MS in Pharmacy/Pharmaceutical Sciences, Chemistry, or related science required with * BS in Pharmacy/Pharmaceutical Sciences, Chemistry, or related science with 3+ years of applicable product development experience required and direct pharmaceutical drug product development experience preferred. * AS in Pharmacy/Pharmaceutical Sciences, Chemistry, or related science with 15+ years of applicable product development experience required and direct pharmaceutical drug product development experience preferred. * Good laboratory and analytical skills required. * Ability to stand, walk and reach regularly. Required to sit, stand, walk, stoop, kneel, crouch regularly and lift to 15 pounds; no lifting greater than 44.09 pounds without assistance. Ability to work extended hours or off-hours as required. * Vision requirements include ability to differentiate color, have 20/30 vision with or without corrective lenses, read written documents and frequent use of a computer monitor. Why You Should Join Catalent * Comprehensive benefits package including medical, dental, and vision coverage effective day one. * Generous paid time off - 152 hours of PTO plus 8 paid holidays. * Tuition reimbursement and a defined career path with annual performance reviews to support growth. * Inclusive, mission-driven culture with active Employee Resource Groups and community engagement. * Wellness and lifestyle perks through Perkspot discounts and the WellHub program. Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

This is a full-time salaried position, based onsite out of our Tampa, FL or Bridgewater, NJ location. Catalent is seeking a dynamic and experienced Senior Manager, Business Assurance to join our Global Business Assurance team. This high-impact role is responsible for overseeing Internal Controls and SOX compliance for a subset of the organization ensuring the accuracy and integrity of financial reporting. You will work closely with the site Finance Directors, acting as a trusted advisor and strategic partner in driving financial excellence and operational efficiency supporting remediation and enhancement of internal controls. In addition, you will lead one Internal Audit per quarter. The internal audit will be cosourced by one of the big four accounting firms. The Role: Lead the end-to-end SOX 404 compliance process, including planning, walkthroughs, testing, documentation, and remediation Oversee internal control reviews across financial, operational, and technology domains Partner with finance leads to implement effective controls and address audit observations Act as a subject matter expert on internal controls, risk mitigation, and process improvement Lead Internal Audits of Catalent sites or key risk areas and processes Collaborate with senior leadership and external auditors to identify and resolve control deficiencies 25% annual global travel expectations Other duties as assigned The Candidate: Bachelor's degree in Accounting, Finance, or related field, required; CPA, required Minimum seven years of progressive experience in accounting, finance, or audit, ideally within a publicly traded or multinational organization, required Strong understanding of SOX, internal controls, and financial reporting, required Experience with ERP and CRM systems; familiarity with pharmaceutical or life sciences industry, preferred Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds Pay: New Jersey Posting The anticipated salary range for this position in New Jersey is $176,533 - $198,832, plus bonus, when eligible. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states. Why You Should Join Catalent: Defined career path and annual performance review and feedback process 152 hours of PTO + 8 paid holidays Several Employee Resource Groups focusing on D&I Generous 401K match Medical, dental and vision benefits effective day one of employment Tuition Reimbursement WellHub - program to promote overall physical wellness Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

* Work Schedule: 7:30am - 7:30pm - 2/2/3 Work Rotation * 100% on-site Our St. Petersburg, FL location is the primary softgel development and manufacturing facility in North America. The site has the capability to develop lipid formulations in a dedicated pilot plant which supports rapid transition from laboratory scale to clinical supply. The Facilities Technician performs a variety of advanced skilled maintenance on utilities systems in support of the larger manufacturing organization; including but not limited to HVAC repair, painting, water system maintenance, and electrical trades work. The Role: * Performs a variety of routine skilled maintenance on utilities systems in support of the larger manufacturing organization; including but not limited to HVAC repair, painting, water system maintenance, and electrical trades work * Utilizes mechanical and/or electrical skills to perform preventative maintenance, troubleshooting, and repairs to plant facility equipment with minimal supervision or mentorship * Ensures that facilities are available for use and consistently maintained in a safe and clean condition * Track, organize, and execute appropriate PM/CM within assigned timeline with minimal supervision * Support your own work orders for equipment activities * Required to read, understand, and follow GMP documents * Other duties as assigned The Candidate: * Must have Associate's Degree with 1+ years of relevant experience OR High School diploma or GED with 3+ years of relevant experience OR High School Diploma or GED with vocational training certificate or diploma * Technical Certificate or higher is preferred * Possesses intermediate mechanical and/or electrical skills and education * Intermediate machine shop and hand tools skills is required * Must be proficient with computers to complete and manage electronic work orders * Must be able to read and understand English-written job instructions and safety requirements * Individual may be required to sit, stand, walk regularly and occasionally lift up to 50 pounds; no lifting greater than 40.09 pounds without assistance Why you should join Catalent: * Defined career path and annual performance review and feedback process * Diverse, inclusive culture * Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives * 152 hours of PTO + 8 paid holidays * Generous 401K match * Medical, dental and vision benefits * Tuition Reimbursement - Let us help you finish your degree or start a new degree! Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

The Quality Assurance Specialist is responsible for managing and documenting events / discrepancies associated with either product or process as well as managing / writing any investigations that may be a result of those event; processing and investigating customer / consumer product complaints; preparing annual product reviews; and, tracking and trending and follow-up of the CAPA program. **Position Summary** This position is 100% on-site at the St. Petersburg site. St. Petersburg is our primary soft gel development and manufacturing facility in North America with capacity of 18 billion capsules per year. Within the Catalent network, we offer a broad range of integrated formulation and analytical services to solve difficult development and manufacturing challenges. The Quality Assurance Specialist interacts directly with manufacturing personnel and is responsible for maintaining a high-quality environment within the manufacturing area by overseeing and ensuring compliance with current Good Manufacturing Practices and Standard Operating Procedures through the periodic inspections and monitoring of process controls in all applicable areas of the manufacturing operation. **The Role** + Collaborates with management and supervisory personnel from Operations, Quality Control and Quality Assurance to resolve problems affecting product quality; collaboration includes reacting, investigating and following up with Operations for non-conformance issues and a working jointly towards resolution. + Provide guidance and plan of action to the manufacturing floor when production events occur as defined by SOP and lead investigations of non-compliant issues according to procedures as defined by SOPs. + Prepare complaint investigation reports and work closely with others on site events to verify scope of investigations, assure root cause analysis and batch impact assessment are adequate, and recommend corrective actions to prevent deviation recurrence; ensure on time closure. + May author other types of quality system documents as directed or assigned by QA management. + Liaise with customers to ensure customer requirements are satisfied. + Facilitate CAPA commitments and Effectiveness Checks, including initiation, tracking, trending, and closure + Prepare annual product reports and ensure on time closure. + Other duties as assigned. **The Candidate** + Bachelor's Degree in Science or related field required (Chemistry, Microbiology or Biology); + A minimum of three years related experience in QA pharmaceutical manufacturing. + Prior experience working with investigation writing, including root cause analysis and report writing a must (prior experience with preparing annual product reviews preferred). + Working knowledge of cGMPs and/or OSHA regulations required. + Ability to work effectively under pressure to meet deadlines. Individual may be required to sit, stand, walk regularly and occasionally lift to 15 pounds; no lifting greater than 44.09 pounds without assistance. Be accessible to manufacturing floor and office staff and to use required office equipment. Specific vision requirements include reading of written documents and frequent use of computer monitor. **Why You Should Join Catalent** + Competitive medical benefits and 401K + 152 hours of PTO + 8 Paid Holidays + Dynamic, fast-paced work environment + Opportunity to work on Continuous Improvement Processes **Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers (*********************************** to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE (*************************************************************************************************************************** .

+ **Work Schedule** : Rotating 12-hour shift from 7:00AM to 7:00PM EST, operating on a two-week cycle. Week 1 includes Monday, Tuesday, Friday, Saturday, and Sunday; Week 2 includes Wednesday and Thursday. + 100% on-site Join Catalent's flagship softgel development and manufacturing facility in North America, located in St. Petersburg, FL, with a capacity of 18 billion capsules per year. This role offers competitive pay, day-one benefits, and career growth in a state-of-the-art, turn-key facility. As an Encapsulation Operator, you will contribute to the manufacturing of pharmaceutical softgels, gaining hands-on experience with multiple technologies and equipment. You'll also collaborate with the on-site Product Development team to support new product innovations. **The Role** + Operates and maintains up to two encapsulation machines, covering up to four during breaks. + Manufactures softgels by following batch record instructions and cGMP standards, completing all required documentation. + Troubleshoot equipment issues to maintain consistent product quality and minimize downtime. Coordinates with crib mechanics during machine changeovers; performs teardown and setup when utilities are unavailable. + Monitors material and gel usage, ensuring components are used within expiration limits and replenishing solvents/lubricants as needed. + Maintains a clean work area, performs in-process quality checks, and ensures timely transport of empty receivers. + Assembles, handles, and stages tray stacks with manufactured softgels; ensures department supplies are stocked. + Handles non-hazardous, hazardous, and DEA-regulated materials and waste in compliance with safety protocols. + Other duties as assigned. **Qualifications** + High school diploma or equivalent required + Previous manufacturing experience in a GMP-regulated industry preferred + Ability to sit, stand, walk, and lift up to 30 lbs regularly during a 12-hour shift; must be able to access the manufacturing floor + No lifting over 44.09 lbs without assistance; must be able to push/pull up to 500 kg (approximately 1,100 lbs) + Must pass Ishihara Color Vision Screening and achieve 20/30 visual acuity (near and far), with or without corrective lenses + Primary workstation is in a high-noise manufacturing area with exposure to industrial chemicals, detergents, flammable materials, and potent drug compounds; annual physical required for handling potent compounds + Work schedule may include nights, weekends, and overtime as needed **Why You Should Join Catalent** + Tuition reimbursement to support educational goals + 152 hours of PTO plus 8 paid holidays & Medical, dental, and vision benefits effective day one + WellHub program to promote physical wellness & Access to Perkspot discounts from over 900 merchants + Defined career path with annual performance reviews + Inclusive culture with active Employee Resource Groups & Community engagement and green initiatives + Strong potential for career growth within a mission-driven organization **Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers (*********************************** to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE (*************************************************************************************************************************** .

Work Schedule: Monday - Friday, standard business hours 100% on-site Join Catalent's flagship softgel development and manufacturing facility in North America, located in St. Petersburg, FL, with a capacity of 18 billion capsules per year. This role offers competitive pay, day-one benefits, and career growth in a state-of-the-art, turn-key facility. The Senior Project Engineer is responsible for providing technical expertise and management of projects primarily involving the upgrade, installation, troubleshooting, and optimization of process and FAC/UtL equipment and small-scale construction projects. This includes projects supporting new product introduction (NPI), equipment reliability & total productive maintenance (TPM), cost containment, efficiency improvements, and regulatory compliance. The position is responsible to interface with internal stakeholders, suppliers, contractors, and external customers. The Role Initiate and manage capital projects ($5K-$1M+), including forecasting and milestone expenditure reporting. Prepare, manage, and communicate project plans for major projects. Provide engineering technical guidance, generate and document functional requirements and design specifications. Lead procurement, design approval, construction, installation, and commissioning of new or modified equipment or areas. Provide technical recommendations for process development, troubleshooting, and maintenance of equipment. Lead ergonomic and safety assessments, maintain CMMS asset information, and generate equipment SOPs. Support site Quality (cGMP) and EHS compliance, lead impact assessments, investigations, and CAPAs. Drive cost-saving and lean initiatives, stay current with new technologies, and mentor or supervise team members. Other duties as assigned. The Candidate Bachelor's degree in engineering, physics, mathematics, or other discipline relevant to the project engineering function required. 8+ years' project engineering experience in a regulated manufacturing industry required, preferably working with pharmaceutical drug products. An advanced technical degree may be substituted for years of experience. Demonstrated success with large ($250k+) capital project management in area of technical expertise. Individual may be required to sit, stand, walk regularly and occasionally lift up to 20 pounds, no lifting greater than 44 pounds without assistance. Specific vision requirements include reading of written documents and use of computer monitor screen frequently. Why You Should Join Catalent Tuition reimbursement to support educational goals 152 hours of PTO plus 8 paid holidays & Medical, dental, and vision benefits effective day one WellHub program to promote physical wellness & Access to Perkspot discounts from over 900 merchants Inclusive culture with active Employee Resource Groups & Community engagement and green initiatives Strong potential for career growth within a mission-driven organization Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

**Senior Contract Specialist** **This is a full-time salaried position, onsite expectations our of Tampa, FL or Bridgewater, NJ.** **The Senior Contract Specialist** serves as a business partner to our Business Development and Legal organizations. **The Senior Contract Specialist** will support the development and execution of contracts with new and existing customers ensuring Catalent has strong, profitable contracts with business terms that align with guidelines and represent a win-win for Catalent and our customers. The **Senior Contract Specialist** is also accountable for organizing internal stakeholders, subject matter experts, Legal and supporting functions across the global Catalent organization to provide for long-term sustainable contracts. **The Role:** + Negotiate contracts in partnership with Business Development, Legal and other functional leads to achieve timely deal closure and growth expectations + Mitigates risk through understanding of proposed terms and conditions and develops recommendations for contract language to meet business needs + Identify and communicate risk areas throughout the negotiation contract lifecycle and the renewal process. Escalate issues appropriately + Drive compliance with Legal, organizational and departmental policies and procedures with adherence to processes and business rules + Experience leading contract negotiations and drafting contracts + Demonstrated knowledge of contract terms and terminology enabling a comprehensive review and commentary of business contracts + Other duties as assigned **The Candidate:** + Bachelor's degree, required + Minimum of five years of contracting and negotiating experience, with relevant experience in the Pharmaceutical, Biotechnology or Consumer Health industries + Experience leading contract negotiations and drafting contracts + Demonstrated knowledge of contract terms and terminology enabling a comprehensive review and commentary of business contracts + Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds **Pay:** **New Jersey Posting** The anticipated salary range for this position in **New Jersey** is **$100,000 - $130,000** , plus bonus, when eligible. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states. **Why You Should Join Catalent:** + Defined career path and annual performance review and feedback process + 152 hours of PTO + 8 paid holidays + Several Employee Resource Groups focusing on D&I + Generous 401K match + Medical, dental and vision benefits effective day one of employment + Tuition Reimbursement **Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers (*********************************** to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE (*************************************************************************************************************************** .

Work Schedule: Monday through Friday, Standard Hours 100% on-site Join Catalent's flagship softgel development and manufacturing facility in North America, located in St. Petersburg, FL, with a capacity of 18 billion capsules per year. This role offers competitive pay, day-one benefits, and career growth in a state-of-the-art, turn-key facility. The Associate Scientist II, Quality Control role is responsible for independently performing testing and developing assays to identify and characterize raw materials, in-process samples, stability samples, and finished products. The position involves analyzing and documenting data in compliance with cGMP and internal guidelines, communicating results, and supporting procedures, specifications, and test method development. This role is fully on-site in St. Petersburg and includes training colleagues, continuous improvement efforts, and strict adherence to FDA, EPA, OSHA, and safety requirements. The Role Analysis of finished products, in-process materials, fill moisture, raw materials, and cleaning verification and validation samples according to the assigned specifications, methods and protocols. Performs analysis of finished products, validation samples, in-process materials and raw materials, moisture testing, Gas, Water and manufacturing environmental sampling and testing according to the effective Specifications, protocols, Methods and Compendial monograms. Cultivate and identify bacteria or other microorganisms isolated on selective and non-selective media. Maintains cultures according to ATCC and departmental Standard Operating Procedures. Performs identification of microorganisms using techniques such as API, Gram Stain, etc. Prepares reagents, standards, Medias, etc. needed for analysis. Interprets and tabulates results of analysis. Records the results in approved notebooks, reports and logbooks. Other duties as assigned. The Candidate Requires BS or BA with college course work in related sciences. Analytical laboratory experience preferred but not required. Experience with common pharmaceutical laboratory equipment including but not limited to: experience with U.V. spectroscopy experience with IR and AA instrumentation, H.P.L.C. and G.C. instrumentation experience, Autoclave, Vitek, and dissolution testing. Expertise in wet chemistry techniques such as titrations, extractions, digestions and preparations of test solutions. Individual may be required to sit, stand, walk regularly and occasionally lift to 15 pounds; no lifting greater than 44.09 pounds without assistance. Vision requirements include ability to differentiate color (Pass the Ishihara Color Vision Screening) and obtain 20/30 acuity in both far and near vision with or without corrective lenses. For Catalent's in-house screening, the acceptable score is to identify at least 4 of 6 numbers in the circles. Why You Should Join Catalent Competitive medical benefits and 401K 152 hours of PTO + 8 Paid Holidays Dynamic, fast-paced work environment Opportunity to work on Continuous Improvement Processes Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. This is a full-time salaried position, onsite in St Petersburg, FL. The Controller is responsible for creating an environment of good internal control and accounting practice for the St Pete Softgel facility. The position is key contributor in the establishment and maintenance of disciplined financial process in a fast-paced growth environment. The position is responsible for coordinating all the activities to ensure an accurate, on time month end close and reporting process in accordance with head office deadlines. The incumbent in this role will work in collaboration with the FP&A Manager and Cost Accounting Manager to ensure a good governance environment across the organization. The position will play a key role in the development, attraction and retention of two direct reports. The Controller is also supported by the Shared Services group who provide Accounts Receivable, Accounts Payable and General Accounting support to the facility. The incumbent has a critical role partnering with the offshore Shared Services team to ensure that an effective and efficient service is provided and follow up with any aging balance through the proper reconciliations and agreed action plans. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee. The Role: Ensure that the Business Unit is compliant with Catalent's financial policies and procedures and generally accepted accounting principles (USGAAP) Provide overall direction for the month end close process Ensure that the financial statements clearly reflect the current situation of the business through the correct revenue recognition, the required journal entries and the creation of accruals and provisions to recognize on time the expenses and liabilities that the business could have Ensure timely and accurate financial results are reported using the GL and Reporting Systems Responsible for all reporting requirements (JD Edwards, OneStream, monthly/quarterly closing, forecast, budget, etc. Responsible for the maintenance and integrity of the site transactional systems, including general ledger, accounts receivable, accounts payable, and fixed asset sub ledgers Ensure that balances in Balance Sheet are accurate and up to date through the definition and establishment of the proper reconciliation methodology for each account based on its nature Serve as the liaison between the site and both internal and external audit teams Responsible for satisfying external (Grant Thornton/KPMG, customer requests, Tax audits) and internal audit requirements Other duties as assigned The Candidate: Bachelor's degree in Accounting or Finance, required; CPA, preferred Minimum 10 years of experience in accounting Experience within a manufacturing environment or pharmaceutical company, preferred Proficiency level using Excel and Access database, required Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience Why You Should Join Catalent: Defined career path and annual performance review and feedback process Diverse, inclusive culture 152 hours of PTO + 8 paid holidays Several Employee Resource Groups focusing on D&I Dynamic, fast-paced work environment Positive working environment focusing on continually improving processes to remain innovative Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives Community engagement and green initiatives Generous 401K match Medical, dental and vision benefits effective day one of employment Tuition Reimbursement WellHub - program to promote overall physical wellness Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

+ **Work Schedule** : Monday - Friday, standard business hours + 100% on-site Join Catalent's flagship softgel development and manufacturing facility in St. Petersburg, FL, producing 18 billion capsules annually. This role offers competitive pay, day-one benefits, and career growth in a state-of-the-art facility, where your work directly impacts patient lives. Product Development oversees end-to-end product creation, including benchtop/lab-scale work, feasibility batches, registration/stability batches, and technical support for process validation. The team also supports product investigations, technology transfers to the St. Petersburg, FL facility, and conducts Gap Assessments, Risk Assessments, and implementation of PAT solutions. This role plays a critical part in the timely development of new pharmaceutical products using Softgel formulation and process technologies by executing essential formulation and process activities. **The Role** + Leads and executes experimental studies to generate supporting data and resolve technical issues throughout project lifecycles. + Represents Softgel Product Development in internal and customer meetings, clearly communicating technical objectives. + Collaborates closely with Analytical Services, Operations, QC, QA, and cross-functional partners to meet all project requirements. + Troubleshoots technical challenges, evaluates solution options, and recommends preferred paths forward. + Manages workload independently, identifying potential risks to timelines and escalating unresolved issues appropriately. + Drives process and procedural improvements that enhance efficiency, safety, and overall quality. + Completes technical activities, development reports, and regulatory support documentation while maintaining required training and compliance. + Supports and mentors Softgel personnel as needed, ensuring alignment with departmental and company policies. + Other duties as assigned. **The Candidate** + BS in scientific field with 5 plus years' experience in lab, 3 in GMP OR + MS in scientific field with 3 plus years' experience in GMP lab OR + Doctorate in scientific field with 1 plus years' experience in lab. + Familiarity with batch processing in a pharmaceutical, cGMP environment. Strong knowledge of cGMP Regulatory requirements for process development, technical transfer, and process changes required with basic to advanced statistical analysis and calculations preferred required. + Ability to work effectively under pressure to meet deadlines. Individual may be required to sit, stand, walk regularly and occasionally lift to 15 pounds; no lifting greater than 44.09 pounds without assistance. + Vision requirements include ability to differentiate color (Pass the Ishihara Color Vision Screening) and obtain 20/30 acuity in both far and near vision with or without corrective lenses. For Catalent's in-house screening, the acceptable score is to identify at least 4 of 6 numbers in the circles. **Why You Should Join Catalent** + Comprehensive benefits package including medical, dental, and vision coverage effective day one. + Generous paid time off - 152 hours of PTO plus 8 paid holidays. + Tuition reimbursement and a defined career path with annual performance reviews to support growth. + Inclusive, mission-driven culture with active Employee Resource Groups and community engagement. + Wellness and lifestyle perks through Perkspot discounts and the WellHub program. **Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers (*********************************** to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE (*************************************************************************************************************************** .