Principal research scientist jobs in Greenville, NC - 27 jobs

Join Us and Make a Difference! At Thermo Fisher Scientific, your work will make a global impact. From protecting the environment to ensuring food safety and supporting life-saving cancer research, we address the world's toughest challenges. About The Role: We need a committed Staff R&D Scientist to lead and assist in developing, optimizing, and validating innovative manufacturing processes. The main focus will be on Oral Solid Dose (OSD) Continuous Manufacturing. You will conduct experiments, analyze data, support product validations, and ensure smooth technology transfers to meet client and regulatory requirements. Experience applying data science or statistical analysis tools (e.g., Python, MATLAB) to support process development and optimization is highly desirable. Your expertise will be essential in achieving our ambitious goals and making a significant industry impact. Key Responsibilities: Develop, scale up, and optimize OSD manufacturing processes, focusing on both continuous and batch operations. Design and run experiments using statistical and data science tools to enhance process and product performance. Serve as the technical lead in client discussions, providing scientific rationale for process decisions. Lead technology transfers from R&D to commercial manufacturing with a focus on robustness and compliance. Collaborate with quality, operations, validation, and analytical teams to advance development and commercialization. Apply emerging technologies and industry trends to drive innovation and efficiency. Maintain compliance with regulatory, safety, and quality standards throughout development activities. Education: Bachelor's degree in chemical engineering, chemistry, pharmacy, or a related field with 4+ years of experience, preferrable within oral solid dose, Master's degree with 2+ years, or Ph.D. with no experience required. Experience: Proven experience in manufacturing, specifically in product or process development. This includes scale-up and technology transfer for immediate and controlled-release dosage forms. In-depth knowledge of GMP, process validation, and regulatory requirements. Strong problem-solving, communication, and project management skills. Proficiency in programming languages such as Python or MATLAB. Solid understanding of statistical tools and their application in process development. Advanced knowledge of continuous manufacturing is preferred. Why Thermo Fisher Scientific? Career Development: Opportunities for learning, growth, and leadership. Benefits: Competitive pay, healthcare, retirement plans, and more. Inclusive Culture: We value different perspectives and cultivate an encouraging environment. Purposeful Work: Join a team that's making a tangible difference in the world. Do you thrive in dynamic environments and love solving sophisticated challenges? If so, we want to hear from you. Reasonable Accommodations We are committed to providing reasonable accommodations to individuals with disabilities. If you require assistance during the application process, please contact our HR team. Thermo Fisher Scientific is an Equal Opportunity Employer. We value diversity and do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.

Job Description Job Title: Aquatic Technology Development Scientist Department Name: Research Supervisor Title: Director of Research, Regulatory, and Innovation JOB SUMMARY SePRO Corporation is dedicated to discovering and developing improved, sustainable solutions to manage aquatic resources. Founded in 1994, SePRO's ongoing mission is to protect, preserve, and restore the environment including aquatic ecosystems of all sizes. We have a history of successful technological innovation and unmatched technical support for the management of aquatic invasive species, nuisance and harmful algae, nutrient pollution in water, and overall water quality. EutroPHIX, a division of SePRO, is a leading environmental consultancy and restoration organization specializing in the restoration and management of freshwater ecosystems. EutroPHIX's mission is to address the growing challenge of water quality degradation in lakes, rivers, and wetlands, with a focus on combating eutrophication and enhancing biodiversity. The Aquatic Technology Development Scientist is primarily responsible for supporting the EutroPHIX teams with technical support and project management, as well as research and development of water quality products and product concepts for the SePRO portfolio. PRIMARY RESPONSIBILITIES Provide technical support and project management to the EutroPHIX team with a focus on nutrient management, harmful algae bloom management, water quality improvement, and other water resource management. Specifically, this role provides support for making technical recommendations for water quality management in ponds, lakes, reservoirs, and other water bodies, and providing overall technical support to large government/stakeholder programs engaged in these efforts. Interaction is expected with EutroPHIX Water Quality Technical Specialists, key private applicators/consultants, and state and regulatory agencies; report generation is expected to be part of role to document results and expand market opportunities. A fair amount of time will be spent traveling with Technical Specialists and working with government agencies or permitting authorities to address technical issues pertaining to the use of SePRO products. Lead research and development activities to design and test new SePRO Water products and concepts for water quality management and restoration. This position is responsible for developing SePRO's existing products and new concepts focused on the unmet needs for water quality management and restoration. This will involve designing and conducting studies to address technical questions, developing lab and field studies to support use of products, and working with field personnel to generate data to optimize use directions/efficacy. It is expected that trials will be established in the field with research cooperators and at the SePRO Research and Technology Campus (SRTC), and presentations will be made at regional and national scientific and professional society meetings to highlight ongoing development projects. Represent EutroPHIX to customers; lake management groups; professional lake consultants; federal, state, and local regulators; and university research scientists. This position will be the main point of contact for university and government researchers and will also represent EutroPHIX to business partners and centers of influence (COIs), end users, and university collaborators through field visits and presentations at customer meetings, trade shows, and scientific meetings. EDUCATION, QUALIFICATIONS, AND EXPERIENCE Minimum of M.S. degree in Biogeochemistry, Aquatic Ecology, Limnology, Freshwater Biology, or Algae Management, with a focus on aquatic plants, algae management, and/or lake management. 5+ years of experience in applied aquatic resource management, such as identification and control of aquatic weeds, management of nuisance and harmful algae, and water quality improvement is highly preferred. Experience with applied research and data collection, analysis, and summarization is also highly preferred. Excellent presentation and communication skills and the ability to positively interact with a variety of customers and stakeholders, including internal sales, marketing, and R&D colleagues; government regulatory agencies; professional lake consultants; university cooperators and researchers; and the general public. Ability to travel on a regular basis to conduct and view research trials, visit cooperators/collaborators, provide technical support to EutroPHIX colleagues, and represent EutroPHIX at customer events and professional meetings. Overnight travel is expected approximately 30% of the time. Proficiency with computer software including Excel, Word, PowerPoint, SharePoint, Teams, R, SigmaPlot, and other research, data management, and GIS programs.

The Senior Development Scientist leads and supports formulation and process development activities while serving as a primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities. The Senior Development Scientist is responsible for supporting these activities in the areas of supervision, process development, clinical trial batch manufacturing, packing and documentation. Position Summary This position is 100% on-site at the Greenville site. Catalent's Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development. The Senior Development Scientist will independently design, coordinate, and execute all product development activities including material characterization, excipient selection, prototype manufacture, equipment selection, generation of batch records, scale-up, QbD, and registration batch activities The Role Work closely with analytical scientists, project management, quality, and commercial operations to ensure that formulation and process development are appropriate and timely. Write all the required documentations such as batch records, product development reports, risk assessments, and campaign summaries. Communicate effectively with internal staff, clients, and external vendors. Responsible for GMP compliance in formulation and process development. Support and contribute to qualification of facility and equipment. Coordinate with logistics and scheduling groups to help ensure that an adequate inventory of raw materials is maintained at all times. Maintain competence and training documentation for relevant equipment and processes. All other duties as assigned. The Candidate Bachelor's degree in pharmaceutical science, chemistry, engineering or related science with at least ten years of industrial pharmaceutical experience required or; Master's degree in pharmaceutical science, chemistry, or related science with at least nine years of industrial pharmaceutical experience required or; Ph.D. in Pharmaceutical Science or related field or Pharm.D. with at least seven years of industrial product development experience required. Some exposure to hazardous chemicals and other active chemical ingredients. Capacity to handle and manipulate objects using hands and arms. Ability to occasionally lift items in excess of 50 pounds. This position requires that a respirator be worn for your safety, and as such, employment is contingent upon being able to complete a medical evaluation with satisfactory results. The medical evaluation is conducted via an external vendor assigned by Catalent. 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.

· Responsible for general laboratory and operational support. · At least 5 years' experience in a GMP regulated environment supporting laboratory operations. · This individual will be required to review data from wet chemical techniques including visual evaluation, titrations and pH as well as from instrumental techniques including AA, HPLC, GC and UV/Vis. In addition to data review, this individual will be responsible for reviewing data according to DEA, FDA, and ICH guidelines, as needed. Experience with Empower and LIMS is preferred. · Major duties and responsibilities: · Function as a dedicated data reviewer for the Chemical Quality Lab. · Prioritizes data review and testing with guidance from Supervision. · Assists in monitoring laboratory metrics associated with turnaround goals. · Please list out the (up to) top 3 critical skills: · 1. Function as a dedicated data reviewer for the Chemical Quality Lab. · 2. Prioritizes data review and testing with guidance from Supervision. · 3 Assists in monitoring laboratory metrics associated with turnaround goals · How do you define "quality"?: qualified reliable team player · How many years' experience are required?: 3-5 years · What is the minimum education experience required?: BS Qualifications · BS in Chemistry

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Responsible for general laboratory and operational support. • BS in Chemistry • At least 5 years experience in a GMP regulated environment supporting laboratory operations. This individual will be required to review data from wet chemical techniques including visual evaluation, titrations and pH as well as from instrumental techniques including AA, HPLC, GC and UV/Vis. In addition to data review, this individual will be responsible for reviewing data according to DEA, FDA, and ICH guidelines, as needed. Experience with Empower and LIMS is preferred. MAJOR DUTIES AND RESPONSIBILITIES: 1. Function as a dedicated data reviewer for the Chemical Quality Lab. 2. Prioritizes data review and testing with guidance from Supervision. 3. Assists in monitoring laboratory metrics associated with turnaround goals. Qualifications BS Additional Information For more information, Please contact Akriti Gupta Associate Recruiter(Scientific & Clinical Division) Office: ************ | Fax: ************

Join Us and Make a Difference! At Thermo Fisher Scientific, your work will make a global impact. From protecting the environment to ensuring food safety and supporting life-saving cancer research, we address the world's toughest challenges. About The Role: We need a committed Staff R&D Scientist to lead and assist in developing, optimizing, and validating innovative manufacturing processes. The main focus will be on Oral Solid Dose (OSD) Continuous Manufacturing. You will conduct experiments, analyze data, support product validations, and ensure smooth technology transfers to meet client and regulatory requirements. Experience applying data science or statistical analysis tools (e.g., Python, MATLAB) to support process development and optimization is highly desirable. Your expertise will be essential in achieving our ambitious goals and making a significant industry impact. Key Responsibilities: * Develop, scale up, and optimize OSD manufacturing processes, focusing on both continuous and batch operations. * Design and run experiments using statistical and data science tools to enhance process and product performance. * Serve as the technical lead in client discussions, providing scientific rationale for process decisions. * Lead technology transfers from R&D to commercial manufacturing with a focus on robustness and compliance. * Collaborate with quality, operations, validation, and analytical teams to advance development and commercialization. * Apply emerging technologies and industry trends to drive innovation and efficiency. * Maintain compliance with regulatory, safety, and quality standards throughout development activities. Education: Bachelor's degree in chemical engineering, chemistry, pharmacy, or a related field with 4+ years of experience, preferrable within oral solid dose, Master's degree with 2+ years, or Ph.D. with no experience required. Experience: * Proven experience in manufacturing, specifically in product or process development. This includes scale-up and technology transfer for immediate and controlled-release dosage forms. * In-depth knowledge of GMP, process validation, and regulatory requirements. * Strong problem-solving, communication, and project management skills. * Proficiency in programming languages such as Python or MATLAB. * Solid understanding of statistical tools and their application in process development. * Advanced knowledge of continuous manufacturing is preferred. Why Thermo Fisher Scientific? * Career Development: Opportunities for learning, growth, and leadership. * Benefits: Competitive pay, healthcare, retirement plans, and more. * Inclusive Culture: We value different perspectives and cultivate an encouraging environment. * Purposeful Work: Join a team that's making a tangible difference in the world. Do you thrive in dynamic environments and love solving sophisticated challenges? If so, we want to hear from you. Reasonable Accommodations We are committed to providing reasonable accommodations to individuals with disabilities. If you require assistance during the application process, please contact our HR team. Thermo Fisher Scientific is an Equal Opportunity Employer. We value diversity and do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. DESCRIPTION: Join our team at Thermo Fisher Scientific as an MSAT TT Scientist III and make meaningful contributions to pharmaceutical development. In this role, you'll lead complex technical projects involving formulation development, process optimization, and technology transfer for pharmaceutical products. Working with advanced analytical technologies and equipment, you'll develop and validate scientific methodologies while ensuring compliance with GMP standards. You'll serve as a technical subject matter expert, collaborating with cross-functional teams and clients to implement innovative solutions that advance drug development from pre-clinical through commercialization stages. Discover Impactful Work · Technically supports day-to-day operations in the Formulation, Filling, and/or Freeze Drying areas of the Steriles plant. · Leads technical/scientific process/product/project activities to implement strategies and technical solutions. · Drives creation of processes, single use systems, and equipment designs for clinical, scale up, and/or registration batches, including technology transfer of projects from clients. · Makes decisions that involve direct application of technical knowledge. A Day in the Life · Design, implement, and evaluate studies, lead tech transfer, commercial scale-up and support process validation. · Represent the organization on formal technical and scientific forums. · Lead and/or participate in problem solving and project work for formulations, equipment and processes. · Write/revise work orders for new processes, FORMs, reports, memos, and protocols as required. · Independently manage projects, proficient in evaluating and organizing all technical aspects of the project to achieve necessary landmarks and turning points. · Support manufacturing operations, change controls, investigations as subject matter expert (SME), resolve accurate CAPAs. · Assess material changes and determine change impact. · Support development of proposals and timelines for projects, leading relevant client meetings. · Review new bid quotes, protocols, technical documents, results, and reports. REQUIREMENTS: • Advanced degree plus 3 years of experience, or Bachelor's degree plus 5 years of pharmaceutical industry experience • Preferred Fields of Study: Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, Engineering or related scientific field • Expertise in analytical techniques including HPLC, GC, LC/MS, spectroscopy and related instrumentation • Strong knowledge of GMP requirements and pharmaceutical regulatory guidelines • Experience with method development, validation and technology transfer • Demonstrated ability to manage multiple complex technical projects simultaneously • Excellent documentation skills for technical reports, protocols and regulatory submissions • Strong data analysis and statistical evaluation capabilities • Experience presenting technical information to clients and cross-functional teams • Proficiency with Microsoft Office applications and analytical software • Advanced problem-solving and troubleshooting abilities • Strong written and verbal communication skills • Experience supporting and developing team members through technical guidance • Physical requirements include standing/walking, lifting up to 35 lbs, and manual dexterity for lab work • Ability to work safely with laboratory chemicals and equipment while following SOPs • Experience in a contract manufacturing organization (CMO) preferred • Knowledge of aseptic techniques and sterile manufacturing preferred for some positions

Lead and support formulation and process development activities while serving as a primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities. Design, coordinate, and execute all product development activities including material characterization, excipient selection, prototype manufacture, equipment selection, generation of batch records/protocols, scale-up, QbD, and registration batch activities. Write all the required documentations including batch records, protocols, product development reports, risk assessments, and campaign summaries. Manage the projects and work with suppliers/vendors, logistics and planner/buyers to help ensure that an adequate inventory of raw materials is maintained at all times. Work closely with analytical scientists, project management, quality, and commercial operations to ensure that formulation and process development are appropriate and timely. Collaborate with quality and analytical groups in performing robust quality event investigations and proposing sound CAPAs. Trouble shoot manufacturing scale up issues during different stages of product development. Work with schedulers to design an efficient schedule of equipment and resources to minimize machine down times and maximize usage of high demand equipment. Maintain competence and training documentation for relevant equipment and processes. EDUCATION AND EXPERIENCE REQUIREMENT: Requires a Master's degree in Pharmaceutical Science and 4 years of experience in job offered or 4 years of experience in the Related Occupation. RELATED OCCUPATION: Sr. Scientist or any other job title performing the following job duties: Designing, coordinating, and executing all product development activities including material characterization, excipient selection, prototype manufacture, equipment selection, generation of batch records/protocols, scale-up, QbD, and registration batch activities. Writing all the required documentations including batch records, protocols, product development reports, risk assessments, and campaign summaries. Managing the projects and working with suppliers/vendors, logistics and planner/buyers to help ensure that an adequate inventory of raw materials is maintained at all times. Working closely with analytical scientists, project management, quality, and commercial operations to ensure that formulation and process development are appropriate and timely. Collaborating with quality and analytical groups in performing robust quality event investigations and proposing sound CAPAs. Trouble shooting manufacturing scale up issues during different stages of product development. Maintaining competence and training documentation for relevant equipment and processes. JOB TIME: Full Time 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.

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Job Description · Responsible for general laboratory and operational support. · At least 5 years' experience in a GMP regulated environment supporting laboratory operations. · This individual will be required to review data from wet chemical techniques including visual evaluation, titrations and pH as well as from instrumental techniques including AA, HPLC, GC and UV/Vis. In addition to data review, this individual will be responsible for reviewing data according to DEA, FDA, and ICH guidelines, as needed. Experience with Empower and LIMS is preferred. · Major duties and responsibilities: · Function as a dedicated data reviewer for the Chemical Quality Lab. · Prioritizes data review and testing with guidance from Supervision. · Assists in monitoring laboratory metrics associated with turnaround goals. · Please list out the (up to) top 3 critical skills: · 1. Function as a dedicated data reviewer for the Chemical Quality Lab. · 2. Prioritizes data review and testing with guidance from Supervision. · 3 Assists in monitoring laboratory metrics associated with turnaround goals · How do you define "quality"?: qualified reliable team player · How many years' experience are required?: 3-5 years · What is the minimum education experience required?: BS Qualifications · BS in Chemistry

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Responsible for general laboratory and operational support. • BS in Chemistry • At least 5 years experience in a GMP regulated environment supporting laboratory operations. This individual will be required to review data from wet chemical techniques including visual evaluation, titrations and pH as well as from instrumental techniques including AA, HPLC, GC and UV/Vis. In addition to data review, this individual will be responsible for reviewing data according to DEA, FDA, and ICH guidelines, as needed. Experience with Empower and LIMS is preferred. MAJOR DUTIES AND RESPONSIBILITIES: 1. Function as a dedicated data reviewer for the Chemical Quality Lab. 2. Prioritizes data review and testing with guidance from Supervision. 3. Assists in monitoring laboratory metrics associated with turnaround goals. Qualifications BS Additional Information For more information, Please contact Akriti Gupta Associate Recruiter(Scientific & Clinical Division) Office: ************ | Fax: ************

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. DESCRIPTION: Join our team at Thermo Fisher Scientific as an MSAT TT Scientist III and make meaningful contributions to pharmaceutical development. In this role, you'll lead complex technical projects involving formulation development, process optimization, and technology transfer for pharmaceutical products. Working with advanced analytical technologies and equipment, you'll develop and validate scientific methodologies while ensuring compliance with GMP standards. You'll serve as a technical subject matter expert, collaborating with cross-functional teams and clients to implement innovative solutions that advance drug development from pre-clinical through commercialization stages. Discover Impactful Work * Technically supports day-to-day operations in the Formulation, Filling, and/or Freeze Drying areas of the Steriles plant. * Leads technical/scientific process/product/project activities to implement strategies and technical solutions. * Drives creation of processes, single use systems, and equipment designs for clinical, scale up, and/or registration batches, including technology transfer of projects from clients. * Makes decisions that involve direct application of technical knowledge. A Day in the Life * Design, implement, and evaluate studies, lead tech transfer, commercial scale-up and support process validation. * Represent the organization on formal technical and scientific forums. * Lead and/or participate in problem solving and project work for formulations, equipment and processes. * Write/revise work orders for new processes, FORMs, reports, memos, and protocols as required. * Independently manage projects, proficient in evaluating and organizing all technical aspects of the project to achieve necessary landmarks and turning points. * Support manufacturing operations, change controls, investigations as subject matter expert (SME), resolve accurate CAPAs. * Assess material changes and determine change impact. * Support development of proposals and timelines for projects, leading relevant client meetings. * Review new bid quotes, protocols, technical documents, results, and reports. REQUIREMENTS: * Advanced degree plus 3 years of experience, or Bachelor's degree plus 5 years of pharmaceutical industry experience * Preferred Fields of Study: Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, Engineering or related scientific field * Expertise in analytical techniques including HPLC, GC, LC/MS, spectroscopy and related instrumentation * Strong knowledge of GMP requirements and pharmaceutical regulatory guidelines * Experience with method development, validation and technology transfer * Demonstrated ability to manage multiple complex technical projects simultaneously * Excellent documentation skills for technical reports, protocols and regulatory submissions * Strong data analysis and statistical evaluation capabilities * Experience presenting technical information to clients and cross-functional teams * Proficiency with Microsoft Office applications and analytical software * Advanced problem-solving and troubleshooting abilities * Strong written and verbal communication skills * Experience supporting and developing team members through technical guidance * Physical requirements include standing/walking, lifting up to 35 lbs, and manual dexterity for lab work * Ability to work safely with laboratory chemicals and equipment while following SOPs * Experience in a contract manufacturing organization (CMO) preferred * Knowledge of aseptic techniques and sterile manufacturing preferred for some positions

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Join our team as an MSAT TT Scientist II at Thermo Fisher Scientific, where you'll contribute to pharmaceutical research and development. You'll perform complex analytical testing, develop and validate methods, and ensure product quality while collaborating with cross-functional teams. This role offers the opportunity to work with advanced technology and contribute to life-changing healthcare solutions. You'll conduct sophisticated chemical and physical testing, lead technology transfer activities, and support manufacturing operations. Working closely with internal teams and clients, you'll help advance pharmaceutical development while maintaining the highest standards of quality and compliance. Discover Impactful Work! Technically supports day-to-day operations in the Formulation, Filling, and/or Freeze Drying areas of the Steriles plant. Works on technical/scientific process/product/project activities to implement strategies and technical solutions. Assists in the creation of processes, single use systems, and equipment designs for clinical, scale up, and/or registration batches, including technology transfer of projects from clients. Makes decisions that involve direct application of technical knowledge. A Day in the Life. Complete studies, tech transfer, commercial scale-up and support process validation. Represent the organization on internal technical discussions. Actively participate in problem solving and project results for formulations, equipment and processes. Write/revise work orders for existing processes, FORMs, reports, memos, and protocols. Lead projects with a moderate level of supervision, implement change control actions, review and plans technical aspects of the project to meet timeline and project goals. Support manufacturing operations, change controls, investigations as subject matter expert (SME). Collects data for statistical analysis. Can support interpretation and summary of data. REQUIREMENTS: • Advanced Degree, no prior experience required, or Bachelor's Degree plus 2 years of experience in pharmaceutical or related industry, preferably in GMP/GLP environment • Preferred Fields of Study: Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or related physical science field • Extensive hands-on experience with analytical instrumentation including HPLC, GC, LC/MS, spectroscopy, and dissolution testing • Strong knowledge of pharmaceutical GMPs, regulatory requirements, and quality systems • Proven expertise in method development, validation, and transfer of analytical methods • Experience with data analysis, interpretation, and technical writing of protocols and reports • Proficiency in Microsoft Office Suite and analytical software systems • Strong analytical and problem-solving capabilities • Demonstrated project management abilities and capacity to manage multiple projects • Effective written and verbal communication skills for both technical and non-technical audiences • Ability to work both independently and collaboratively • Physical requirements include standing for extended periods, lifting up to 35 pounds, and working with laboratory equipment • Must be able to follow safety protocols and wear appropriate PPE as required • Demonstrated alignment with company values of Integrity, Intensity, Innovation, and Involvement

The Development Scientist I serves as a primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities. This role is responsible for supporting these activities in the areas of supervision, process development, clinical trial batch manufacturing, packing and documentation. Position Summary This position is 100% on-site at the Greenville site. Catalent's Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development. The Development Scientist I will design, coordinate, and execute development and CTM activities, including formulation, data interpretation, equipment selection, generation of batch records and other appropriate documentation, and problem-solving exercises. The Role Independently design and execute experiments. Interpret data and make sound recommendations based on data. Solve formulation and process problems. Author SOP's, IQ/OQ/PQ documents, development and technical reports, and CMC sections for regulatory submissions. Maintain competency and training for relevant processes and equipment. Ensure that all work is accurate, precise, properly documented, within GMP requirements. Organize multiple project responsibilities to ensure tasks are appropriately prioritized and executed on time. All other duties as assigned. The Candidate Bachelor's degree in pharmaceutical science, chemistry, engineering, or related science with at least three years of industrial pharmaceutical experience required or; Master's degree in pharmaceutical science or chemistry or related science with at least two years of industrial pharmaceutical experience required or; Ph.D. in Pharmaceutical Science or related field or Pharm.D. with at least one year of industrial pharmaceutical experience preferred. Some exposure to hazardous chemicals and other active chemical ingredients. Position requires the capacity to handle and manipulate objects using hands and arms. Requires ability to occasionally lift items in excess of 50 pounds. This position requires that a respirator be worn for your safety, and as such, employment is contingent upon being able to complete a medical evaluation with satisfactory results. The medical evaluation is conducted via an external vendor assigned by Catalent. Why You Should Work At Catalent Spearhead exciting and innovative projects Fast-paced, dynamic environment High visibility to members at all levels of the organization 152 hours of PTO + 8 paid holidays 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 Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Join our team as an MSAT TT Scientist II at Thermo Fisher Scientific, where you'll contribute to pharmaceutical research and development. You'll perform complex analytical testing, develop and validate methods, and ensure product quality while collaborating with cross-functional teams. This role offers the opportunity to work with advanced technology and contribute to life-changing healthcare solutions. You'll conduct sophisticated chemical and physical testing, lead technology transfer activities, and support manufacturing operations. Working closely with internal teams and clients, you'll help advance pharmaceutical development while maintaining the highest standards of quality and compliance. Discover Impactful Work! * Technically supports day-to-day operations in the Formulation, Filling, and/or Freeze Drying areas of the Steriles plant. * Works on technical/scientific process/product/project activities to implement strategies and technical solutions. * Assists in the creation of processes, single use systems, and equipment designs for clinical, scale up, and/or registration batches, including technology transfer of projects from clients. * Makes decisions that involve direct application of technical knowledge. A Day in the Life. * Complete studies, tech transfer, commercial scale-up and support process validation. * Represent the organization on internal technical discussions. * Actively participate in problem solving and project results for formulations, equipment and processes. * Write/revise work orders for existing processes, FORMs, reports, memos, and protocols. * Lead projects with a moderate level of supervision, implement change control actions, review and plans technical aspects of the project to meet timeline and project goals. * Support manufacturing operations, change controls, investigations as subject matter expert (SME). * Collects data for statistical analysis. Can support interpretation and summary of data. REQUIREMENTS: * Advanced Degree, no prior experience required, or Bachelor's Degree plus 2 years of experience in pharmaceutical or related industry, preferably in GMP/GLP environment * Preferred Fields of Study: Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or related physical science field * Extensive hands-on experience with analytical instrumentation including HPLC, GC, LC/MS, spectroscopy, and dissolution testing * Strong knowledge of pharmaceutical GMPs, regulatory requirements, and quality systems * Proven expertise in method development, validation, and transfer of analytical methods * Experience with data analysis, interpretation, and technical writing of protocols and reports * Proficiency in Microsoft Office Suite and analytical software systems * Strong analytical and problem-solving capabilities * Demonstrated project management abilities and capacity to manage multiple projects * Effective written and verbal communication skills for both technical and non-technical audiences * Ability to work both independently and collaboratively * Physical requirements include standing for extended periods, lifting up to 35 pounds, and working with laboratory equipment * Must be able to follow safety protocols and wear appropriate PPE as required * Demonstrated alignment with company values of Integrity, Intensity, Innovation, and Involvement

The Development Scientist II serves as a primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities. The Development Scientist II is responsible for supporting these activities in the areas of supervision, process development, clinical trial batch manufacturing, packing and documentation. Position Summary This position is 100% on-site at the Greenville site. Catalent's Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development. The Development Scientist II is responsible for all formulation and process development of several ongoing projects including project management and customer contact. The Role Responsible for GMP compliance in formulation and process development. Responsible for assisting with planning and operating within a budget for the pharmaceutical area. Work directly with customers and potential customers to agree on development approaches and scope of work. Independently assist manufacturing group with batch manufacture and packaging/labeling, including set-up and cleaning. Lead efforts in solving formulation and process problems. Directly support with writing batch records, SOPs, IQ/OQ/PQ documents, development/technical reports, and CMC sections for regulatory submissions as directed. Ensure that all work is accurate, precise, properly documented and, when appropriate, performed within GMP guidelines. All other duties as assigned. The Candidate Bachelor's degree in Pharmacy, Chemistry, Biology or related field with eight or more years of experience in pharmaceutical development with focus on solids formulation required or; Master's degree in Pharmacy, Pharmaceutics, Industry Pharmacy, or related field with six or more years of experience in pharmaceutical development required or; Ph.D. in Pharmacy, Pharmaceutics, Industry Pharmacy or related field with four or more years of experience in pharmaceutical development required or; Some exposure to hazardous chemicals and other active chemical ingredients. Position requires the capacity to handle and manipulate objects using hands and arms. Requires ability to occasionally lift items in excess of 50 pounds. This position requires that a respirator be worn for your safety, and as such, employment is contingent upon being able to complete a medical evaluation with satisfactory results. The medical evaluation is conducted via an external vendor assigned by Catalent. Why You Should Work At Catalent Spearhead exciting and innovative projects Fast-paced, dynamic environment High visibility to members at all levels of the organization 152 hours of PTO + 8 paid holidays 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 QC Scientist I performs analytical methods for moderately to complex testing on a variety of cleaning, in process, stability, and release samples in a chemistry environment within defined procedures and practices. Support internal manufacturing operations. Make detailed observations and review, documents and communicate test results; recommend solutions. Typical hours are 3:00pm - 1:30am, Tuesday through Friday, 10 Hour shift Key Responsibilities: Conduct simple chemical and physical testing of pharmaceutical products by internally developed and compendial test methods. Complete validated test methods for finished pharmaceutical products and traditional wet chemical testing. Recognize and report out-of-specification or unexpected results and non-routine analytical and product problems. Clearly and accurately communicate the results of work by documenting the testing/analysis and obtained results. Record and report results in accordance with prescribed lab procedures and systems. Provide communications with outside departments. Write SOPs and other instructional documents. Clean and organize work area, instrumentation, and testing materials. Perform all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines. Maintain the necessary compliance status required by company and facility standards. Qualifications: Associate Degree in Chemistry, Biochemistry, Molecular Biology, or related physical/biological service field minimally required. Bachelor degree preferred. 1+ years related experience performing chemical tests with chromatographic, spectroscopic, or other analytical techniques, working knowledge of Empower is a plus. Good knowledge and understanding of chemistry and analytical instrumental technologies. Good knowledge of qualitative and quantitative tests. Good knowledge of quality and regulatory requirements in the pharmaceutical industry, including pharmaceutical GMPs. Good problem-solving skills and logical approach to solving scientific problems. Good interpersonal and communication skills (both oral and written). Ability to apply mathematical operations. Physical Requirements: Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations. Ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time. Manipulation (lift, carry, move) of light to medium weights of 10-35 pounds. Arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time. Visual acuity to use a keyboard, computer monitor, operating equipment, and read materials for prolonged periods of time. Ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time. PPE: Safety glasses, safety shoes, lab coat, nitrile or similar gloves, safety aprons, organic respirator occasionally.

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) **Job Description** As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Join our team as an MSAT TT Scientist II at Thermo Fisher Scientific, where you'll contribute to pharmaceutical research and development. You'll perform complex analytical testing, develop and validate methods, and ensure product quality while collaborating with cross-functional teams. This role offers the opportunity to work with advanced technology and contribute to life-changing healthcare solutions. You'll conduct sophisticated chemical and physical testing, lead technology transfer activities, and support manufacturing operations. Working closely with internal teams and clients, you'll help advance pharmaceutical development while maintaining the highest standards of quality and compliance. **Discover Impactful Work!** + Technically supports day-to-day operations in the Formulation, Filling, and/or Freeze Drying areas of the Steriles plant. + Works on technical/scientific process/product/project activities to implement strategies and technical solutions. + Assists in the creation of processes, single use systems, and equipment designs for clinical, scale up, and/or registration batches, including technology transfer of projects from clients. + Makes decisions that involve direct application of technical knowledge. **A Day in the Life.** + Complete studies, tech transfer, commercial scale-up and support process validation. + Represent the organization on internal technical discussions. + Actively participate in problem solving and project results for formulations, equipment and processes. + Write/revise work orders for existing processes, FORMs, reports, memos, and protocols. + Lead projects with a moderate level of supervision, implement change control actions, review and plans technical aspects of the project to meet timeline and project goals. + Support manufacturing operations, change controls, investigations as subject matter expert (SME). + Collects data for statistical analysis. Can support interpretation and summary of data. REQUIREMENTS: - Advanced Degree, no prior experience required, or Bachelor's Degree plus 2 years of experience in pharmaceutical or related industry, preferably in GMP/GLP environment - Preferred Fields of Study: Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or related physical science field - Extensive hands-on experience with analytical instrumentation including HPLC, GC, LC/MS, spectroscopy, and dissolution testing - Strong knowledge of pharmaceutical GMPs, regulatory requirements, and quality systems - Proven expertise in method development, validation, and transfer of analytical methods - Experience with data analysis, interpretation, and technical writing of protocols and reports - Proficiency in Microsoft Office Suite and analytical software systems - Strong analytical and problem-solving capabilities - Demonstrated project management abilities and capacity to manage multiple projects - Effective written and verbal communication skills for both technical and non-technical audiences - Ability to work both independently and collaboratively - Physical requirements include standing for extended periods, lifting up to 35 pounds, and working with laboratory equipment - Must be able to follow safety protocols and wear appropriate PPE as required - Demonstrated alignment with company values of Integrity, Intensity, Innovation, and Involvement Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

The Development Scientist II serves as a primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities. The Development Scientist II is responsible for supporting these activities in the areas of supervision, process development, clinical trial batch manufacturing, packing and documentation. **Position Summary** This position is 100% on-site at the Greenville site. Catalent's Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development. The Development Scientist II is responsible for all formulation and process development of several ongoing projects including project management and customer contact. **The Role** + Responsible for GMP compliance in formulation and process development. + Responsible for assisting with planning and operating within a budget for the pharmaceutical area. + Work directly with customers and potential customers to agree on development approaches and scope of work. + Independently assist manufacturing group with batch manufacture and packaging/labeling, including set-up and cleaning. + Lead efforts in solving formulation and process problems. + Directly support with writing batch records, SOPs, IQ/OQ/PQ documents, development/technical reports, and CMC sections for regulatory submissions as directed. + Ensure that all work is accurate, precise, properly documented and, when appropriate, performed within GMP guidelines. + All other duties as assigned. **The Candidate** + Bachelor's degree in Pharmacy, Chemistry, Biology or related field with eight or more years of experience in pharmaceutical development with focus on solids formulation required or; + Master's degree in Pharmacy, Pharmaceutics, Industry Pharmacy, or related field with six or more years of experience in pharmaceutical development required or; + Ph.D. in Pharmacy, Pharmaceutics, Industry Pharmacy or related field with four or more years of experience in pharmaceutical development required or; + Some exposure to hazardous chemicals and other active chemical ingredients. + Position requires the capacity to handle and manipulate objects using hands and arms. + Requires ability to occasionally lift items in excess of 50 pounds. + This position requires that a respirator be worn for your safety, and as such, employment is contingent upon being able to complete a medical evaluation with satisfactory results. The medical evaluation is conducted via an external vendor assigned by Catalent. **Why You Should Work At Catalent** + Spearhead exciting and innovative projects + Fast-paced, dynamic environment + High visibility to members at all levels of the organization + 152 hours of PTO + 8 paid holidays **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** Standard (Mon-Fri) **Environmental Conditions** Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) **Job Description** As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. DESCRIPTION: Join our team at Thermo Fisher Scientific as an MSAT TT Scientist III and make meaningful contributions to pharmaceutical development. In this role, you'll lead complex technical projects involving formulation development, process optimization, and technology transfer for pharmaceutical products. Working with advanced analytical technologies and equipment, you'll develop and validate scientific methodologies while ensuring compliance with GMP standards. You'll serve as a technical subject matter expert, collaborating with cross-functional teams and clients to implement innovative solutions that advance drug development from pre-clinical through commercialization stages. Discover Impactful Work · Technically supports day-to-day operations in the Formulation, Filling, and/or Freeze Drying areas of the Steriles plant. · Leads technical/scientific process/product/project activities to implement strategies and technical solutions. · Drives creation of processes, single use systems, and equipment designs for clinical, scale up, and/or registration batches, including technology transfer of projects from clients. · Makes decisions that involve direct application of technical knowledge. A Day in the Life · Design, implement, and evaluate studies, lead tech transfer, commercial scale-up and support process validation. · Represent the organization on formal technical and scientific forums. · Lead and/or participate in problem solving and project work for formulations, equipment and processes. · Write/revise work orders for new processes, FORMs, reports, memos, and protocols as required. · Independently manage projects, proficient in evaluating and organizing all technical aspects of the project to achieve necessary landmarks and turning points. · Support manufacturing operations, change controls, investigations as subject matter expert (SME), resolve accurate CAPAs. · Assess material changes and determine change impact. · Support development of proposals and timelines for projects, leading relevant client meetings. · Review new bid quotes, protocols, technical documents, results, and reports. REQUIREMENTS: - Advanced degree plus 3 years of experience, or Bachelor's degree plus 5 years of pharmaceutical industry experience - Preferred Fields of Study: Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, Engineering or related scientific field - Expertise in analytical techniques including HPLC, GC, LC/MS, spectroscopy and related instrumentation - Strong knowledge of GMP requirements and pharmaceutical regulatory guidelines - Experience with method development, validation and technology transfer - Demonstrated ability to manage multiple complex technical projects simultaneously - Excellent documentation skills for technical reports, protocols and regulatory submissions - Strong data analysis and statistical evaluation capabilities - Experience presenting technical information to clients and cross-functional teams - Proficiency with Microsoft Office applications and analytical software - Advanced problem-solving and troubleshooting abilities - Strong written and verbal communication skills - Experience supporting and developing team members through technical guidance - Physical requirements include standing/walking, lifting up to 35 lbs, and manual dexterity for lab work - Ability to work safely with laboratory chemicals and equipment while following SOPs - Experience in a contract manufacturing organization (CMO) preferred - Knowledge of aseptic techniques and sterile manufacturing preferred for some positions Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.