Quality control analyst jobs in Lakeland, FL

Within Accenture's Utilities (Energy Retail and Customer Experience) Practice, We use our deep industry expertise in digital customer engagement and operations, connected energy services and customer platforms to help retail energy and utility providers with cost effectiveness, revenue assurance/extension and customer satisfaction and loyalty. In Strategy & Consulting we work with C-suite executives, leaders and boards of the world's leading organizations, helping them reinvent every part of their enterprise to drive greater growth, enhance competitiveness, implement operational improvements, reduce cost, deliver sustainable 360° stakeholder value, and set a new performance frontier for themselves and the industry in which they operate. Our deep industry and functional expertise is supported by proprietary assets and solutions that help organizations transform faster and become more resilient. Underpinned by technology, data, analytics, AI, change management, talent and sustainability capabilities, our Strategy & Consulting services help architect and accelerate all aspects of an organization's total enterprise reinvention. Benefits of Working at Accenture: + Impactful Projects with Leading Clients: Opportunity to partner with top-tier clients in the CNR Industry on transformative projects. + Collaborative Work Culture: Join a dynamic and collaborative environment that values professional growth and development. + Competitive Compensation and Benefits: Enjoy a rewarding compensation package, including extensive benefits. Key Responsibilities: + Lead strategic consulting engagements in energy retail and customer service, focusing on digital transformation, customer experience enhancement, and operational efficiencies. + Serve as a primary client contact for senior executives, building trusted advisory relationships and ensuring alignment with client business objectives. + Develop and execute strategies to improve client business performance, drive revenue growth, and support customer-centric transformation initiatives. + Manage project teams, guiding junior members and ensuring project delivery meets quality, timeline, and budgetary expectations. + Lead business development activities by identifying new opportunities, crafting proposals, and representing Accenture's Utilities practice in sales pursuits. + Actively contribute to thought leadership, staying current on industry trends, regulatory changes, and technological advancements in the energy retail sector. + Drive team development and growth by mentoring team members and fostering a collaborative, high-performance work Note: We are open to hiring in most major cities in the US that are near to an Accenture corporate office. Here's what you need: + Minimum of 3 years of experience in the Utility Industry, Customer Service project delivery / Customer Transformation project delivery + Minimum of 2 years of functional experience with either an SAP or Oracle platform. + Expertise in Meter to Cash operations, functions, and technologies. + Expertise in major Customer Transformation and technology implementations (e.g., CIS replacements) + Bachelor's degree or equivalent work experience. + Ability to travel as needed. Bonus Points If: + You have at least 2 years of experience in an advisory or consulting role Professional Skill Requirements: + You improvise and adapt to lead clients and teams through change and ambiguity + You've gained the trust of your clients and partnered with them to: design business process, lead design thinking workshops, develop business case, deliver agile projects, develop new operating model, manage talent and change, co-create intellectual property Compensation at Accenture varies depending on a wide array of factors, which may include but are not limited to the specific office location, role, skill set, and level of experience. As required by local law, Accenture provides a reasonable range of compensation for roles that may be hired as set forth below. We accept applications on an on-going basis and there is no fixed deadline to apply. Information on benefits is here. (************************************************************ Role Location Annual Salary Range California $63,800 to $205,800 Cleveland $59,100 to $164,600 Colorado $63,800 to $177,800 District of Columbia $68,000 to $189,300 Illinois $59,100 to $177,800 Maryland $63,800 to $177,800 Massachusetts $63,800 to $189,300 Minnesota $63,800 to $177,800 New York/New Jersey $59,100 to $205,800 Washington $68,000 to $189,300 #LI-NA #LI-MP Requesting an Accommodation Accenture is committed to providing equal employment opportunities for persons with disabilities or religious observances, including reasonable accommodation when needed. If you are hired by Accenture and require accommodation to perform the essential functions of your role, you will be asked to participate in our reasonable accommodation process. Accommodations made to facilitate the recruiting process are not a guarantee of future or continued accommodations once hired. If you would like to be considered for employment opportunities with Accenture and have accommodation needs such as for a disability or religious observance, please call us toll free at **************** or send us an email or speak with your recruiter. Equal Employment Opportunity Statement We believe that no one should be discriminated against because of their differences. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law. Our rich diversity makes us more innovative, more competitive, and more creative, which helps us better serve our clients and our communities. For details, view a copy of the Accenture Equal Opportunity Statement (******************************************************************************************************************************************** Accenture is an EEO and Affirmative Action Employer of Veterans/Individuals with Disabilities. Accenture is committed to providing veteran employment opportunities to our service men and women. Other Employment Statements Applicants for employment in the US must have work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States. Candidates who are currently employed by a client of Accenture or an affiliated Accenture business may not be eligible for consideration. Job candidates will not be obligated to disclose sealed or expunged records of conviction or arrest as part of the hiring process. Further, at Accenture a criminal conviction history is not an absolute bar to employment. The Company will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. Additionally, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the Company's legal duty to furnish information. California requires additional notifications for applicants and employees. 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Why Work for Saddle Creek? Saddle Creek Logistics Services succeeds by promoting a diverse, friendly, and respectful teamwork environment. As a vital service provider, we not only make a difference in our community but offer our associates opportunities to enhance their skills, build meaningful careers and end each day with a sense of accomplishment. If you're looking for a family-oriented company that lives by its values and offers competitive pay and benefits, join our team today. Benefits: Weekly pay with skill pay and shift differentials Benefits package including medical, dental, vision and medical reimbursement Medical employee-only premium as low as $5.90/week, $26/month with wellness discounts HSA with annual employer contribution Weekly 401(k) match Vacation immediately upon hire 8 holidays per calendar year Personal time after 90 days EAP and identity theft protection Tuition reimbursement Company paid life insurance and short term disability Note that if you are viewing this posting on an external job board (such as Indeed, LinkedIn, ZipRecruiter, etc.), unless specifically stated in the posting, the provided salary estimates may not be accurate as they are not provided by Saddle Creek. Our recruiters look forward to speaking with you about your background, skills, and compensation requirements. Shift: Monday - Friday, 10am-6:30pm The Quality Control Associate will prioritize inspections, quality audits and work needed to ensure the location Protocols and Standards are met. These audits will focus specifically on our outbound team to ensure all product received is to customer's standards. RESPONSIBILITIES: Visually inspect and/or test all materials shipped into the facility to determine if material meets specifications and standards Audit processes to ensure quality standards and defect ranges are being met. Document audits and maintain appropriate records Process off-specification material as directed Inform Outbound Supervisor of major and critical defects found during inspections Verifies corrective action is taken to resolve defects Participate in location inventories Assign tasks to warehouse personnel through written and/or oral instruction, including: unloading, outbound staging and loading, verifying and labeling of freight. Supervise tasks performed by warehouse personnel. Complete reports and records in a timely manner. Troubleshoot machine and equipment malfunctions and report them to maintenance personnel. Advise associates on care and preservation of product, use of equipment in handling, storing, maintaining, shipping stock, and related problems. Ensure high-quality customer service through assisting associates in warehouse functions when help is needed. Take action and speak to associates when proper safety, quality, and productivity procedures are not being followed. Work cooperatively and productively with other warehouse associates. Adhere to company or site-specific safety policy and guidelines to ensure safe working conditions for self and others. Other duties as assigned KNOWLEDGE Must be eighteen (18) years of age or older. Minimum of two (2) years' experience working in a warehouse environment. High school diploma or general education degree (GED) preferred Must be able to perform any physically exerting duties in a warehouse environment, which may be non-air conditioned or heated, meaning the indoor temperature fluctuates with the seasons. Previous quality assurance role Capable of basic math calculations Able to read and interpret specifications and drawings Able to use standard measuring equipment Able to lift, stand or walk constantly all shift as needed Able to lift up to 50 pounds and not allergic to latex gloves Must be able to pass pre-employment drug screening and background check. Proficiency in Microsoft Office Suite. Experience working with a warehouse management system (WMS). Forklift certificate and/or license. ATTITUDES Self motivated Maintains neat/organized work area and documentation Saddle Creek is an Equal Opportunity employer and an Affirmative Action employer, as required by law. We provide equal employment opportunities to applicants and existing associates and evaluate qualified candidates without regard to race, gender, national origin, ancestry, age, color, religious creed, marital status, genetic information, sexual orientation, gender identity, gender expression, sex (including pregnancy, breastfeeding and related medical conditions), mental or physical disability, medical condition, military and veteran status or any other status or condition protected by applicable federal, state, or local laws, governmental regulations and executive orders. View the EEO poster here. View the E-Verify Posting here. Saddle Creek is committed to providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability to search and apply for a career opportunity, please send an e-mail to Disability.accommodation@sclogistics.com and let us know your contact information and the nature of your request.

At Disney, we're storytellers. We make the impossible, possible. We do this through utilizing and developing cutting-edge technology and pushing the envelope to bring stories to life through our movies, products, interactive games, parks and resorts, and media networks. Now is your chance to join our talented team that delivers unparalleled creative content to audiences around the world. "We create happiness." That's our motto at Walt Disney Parks and Resorts. And it permeates everything we do. At Disney, you'll help inspire that magic by enabling our teams to push the limits of entertainment and create the never-before-seen! The Metalworker QC Inspector is more than just a modern day superhero. They conduct routine inspections on rides and equipment to ensure the safety of our Guests and Cast Members. The Metalworker QC Inspector is expected to complete scheduled inspections by the end of shift and assist with repairs if necessary. The field service position may include work from elevated platforms and confined spaces throughout the Walt Disney World Parks and Resort property. The pay rate for this role in Florida is $33.40 per hour. Select benefits may be provided as part of the compensation package, such as medical, financial, and/or other benefits. To learn more about our benefits visit: ***************************************

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 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. 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 Associate Scientist II, Quality Control will independently test, develop and implement assays useful for the identification and characterization of Raw Materials, pre-capsulation, Stability and Finished Products. In addition, this role will Analyze data, document results, maintain laboratory notebook according to cGMP and Internal guidelines, communicate results in written and oral presentations, help in writing Procedures, Specifications and Test Methods. The Associate Scientist II, Quality Control will keep abreast of literature in field; help train colleagues; contribute to continuous improvement within the group, comply with FDA, EPA and OSHA regulations, performing all work in a safe manner and maintain proper records in accordance with all SOP's and policies. This position is 100% on-site at the St. Petersburg site. **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. Must possess good interpersonal skills. Ability to effectively communicate with co-workers. Good organizational skills 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. + Knowledge of safety and hazardous waste requirements + Knowledge of data acquisition applications and databases + Experience in conducting and writing laboratory investigations + 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** + 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 (*************************************************************************************************************************** .

Morgan Stanley is a leading global financial services firm providing a wide range of investment banking, securities, investment management and wealth management services. The Firm's employees serve clients worldwide including corporations, governments and individuals from more than 1,200 offices in 43 countries. As a market leader, the talent and passion of our people is critical to our success. Together, we share a common set of values rooted in integrity, excellence and strong team ethic. Morgan Stanley can provide a superior foundation for building a professional career - a place for people to learn, to achieve and grow. A philosophy that balances personal lifestyles, perspectives and needs is an important part of our culture. Department Profile: The WM and U.S. Banks Financial Crimes Risk Team is embedded within the Firm's business line. It is responsible for identifying, assessing, and escalating potential money laundering and reputational risk issues associated with higher risk client types. The WM and U.S. Banks Financial Crimes Risk Team is considered the first line of defense and supports the onboarding, enhanced due diligence, and negative news processes for Morgan Stanley. Primary Responsibilities - Review QC findings prepared by the QC Analyst/Manager and focus on analysis of associated risk factors, including any factors that increase or mitigate the risk posed by the error documented - Assist in preparing ongoing and ad hoc reporting for senior management. - Escalate potential risk issues associated with new and existing account customer profiles with internal management and the Second Line of Defense Bank AML Compliance teams. - Contribute to the planning and performance of internal reviews of controls residing within various product and business areas to ensure that controls are adequately designed and are operating effectively. - Assist in maintaining and updating procedures and proposing testing methods or alternative recommendations for process improvements and program efficiency. Experience Required: - Bachelor's degree in related field or an equivalent combination of training and experience - Minimum 7 years of experience in financial crimes/AML compliance testing, Audit or similar related QA/QC testing experience at a financial institution Skills Required: - Expert knowledge of AML regulatory requirements and expectations (Domestic - US and International - non-US), MS WM and U.S. Banks Financial Crimes Risk policies and procedures, KYC standards, and QC Program - Strong communications, analytical, organizational, project management and planning skills to be able to develop QC Testing Program, test scripts, testing reports and metrics reporting and manage testing analysts - Strong managerial experience leading teams of 6-10 people - Strong knowledge of business, products, operations, systems and organization to be able to execute the QC Program - Basic knowledge of MS Office (Microsoft Excel/PowerPoint/Word/Access) - Experience with data and trend analysis related to the management of an AML program - Experience in AML/CFT and/or Legal/Regulatory Compliance Ability to: - Take initiative, analyze, summarize, and communicate effectively - Investigate, identify issues, impacts and trends as a result of QC testing to propose comprehensive solutions for the business unit and/or organization - Multitask effectively and action matters promptly - Work independently and in a team environment - Handle highly confidential information with appropriate discretion. - Work in a high volume, fast paced environment - Work in a matrixed organization, leveraging resources across the organization to perform QC activity and effect change based on QC findings Additional Skills Desired: - Certified as an Anti-Money Laundering Specialist by ACAMS or equivalent AML certification/license/audit/control testing certification (is a plus) WHAT YOU CAN EXPECT FROM MORGAN STANLEY: We are committed to maintaining the first-class service and high standard of excellence that have defined Morgan Stanley for over 89 years. Our values - putting clients first, doing the right thing, leading with exceptional ideas, committing to diversity and inclusion, and giving back - aren't just beliefs, they guide the decisions we make every day to do what's best for our clients, communities and more than 80,000 employees in 1,200 offices across 42 countries. At Morgan Stanley, you'll find an opportunity to work alongside the best and the brightest, in an environment where you are supported and empowered. Our teams are relentless collaborators and creative thinkers, fueled by their diverse backgrounds and experiences. We are proud to support our employees and their families at every point along their work-life journey, offering some of the most attractive and comprehensive employee benefits and perks in the industry. There's also ample opportunity to move about the business for those who show passion and grit in their work. To learn more about our offices across the globe, please copy and paste ***************************************************** into your browser. Expected base pay rates for the role will be between $95K-$170K per year at the commencement of employment. However, base pay if hired will be determined on an individualized basis and is only part of the total compensation package, which, depending on the position, may also include commission earnings, incentive compensation, discretionary bonuses, other short and long-term incentive packages, and other Morgan Stanley sponsored benefit programs. Morgan Stanley's goal is to build and maintain a workforce that is diverse in experience and background but uniform in reflecting our standards of integrity and excellence. Consequently, our recruiting efforts reflect our desire to attract and retain the best and brightest from all talent pools. We want to be the first choice for prospective employees. It is the policy of the Firm to ensure equal employment opportunity without discrimination or harassment on the basis of race, color, religion, creed, age, sex, sex stereotype, gender, gender identity or expression, transgender, sexual orientation, national origin, citizenship, disability, marital and civil partnership/union status, pregnancy, veteran or military service status, genetic information, or any other characteristic protected by law. Morgan Stanley is an equal opportunity employer committed to diversifying its workforce (M/F/Disability/Vet).

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Lonza Tampa is seeking a QC Chemist to join the Quality Control team. The incubment will be Conduct analysis of raw materials, In process items and finished products Key Accountabilities Analysis of dry product stability and finished product samples according to the assigned specifications, analytical methodology and protocols in a GMP laboratory setting with emphasis on attention to detail and accuracy of execution. Documentation of results in accordance with cGMP Comply with FDA, EPA and OSHA regulations, performing all work in a safe manner. Reports lab testing data and completes documentation accurately and in accordance with laboratory procedures and regulatory requirements Reviews results for conformance to standards Perform analytical testing of pharmaceutical products following analytical methodology Read and interpret analytical methodology and the USP Supports method development and validation of new methods Performs investigations and completes CAPA in response to deviations. Develops and executes validation protocols for test methods and equipment qualification as requested. Meet fundamental cGMP requirements relating to conduct and work practices to ensure the SISPQ (Safety, Identity, Strength, Purity, and Quality) of the all products manufactured/tested at Lonza Tampa. Adhere to all defined Safety and Sustainability requirements and expectations and seek clarification whenever Safety and Sustainability requirements and expectations are either unknown or unclear Promptly report identified Safety and Sustainability issues, problems, deficiencies, errors, incidents, and/or opportunities to management and correct where possible Stop work where deemed necessary to maintain safety Key Requirement Associate's Degree in Science, preferably chemistry Minimum of 3 years experience in a GMP pharma environment Actively participates in customer and regulatory audits Demonstrated experience with peer review work and data of other analysts to ensure compliance with method and regulatory requirements Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of. Lonza Tampa is seeking a QC Chemist to join the Quality Control team. The incubment will be Conduct analysis of raw materials, In process items and finished products Key Accountabilities * Analysis of dry product stability and finished product samples according to the assigned specifications, analytical methodology and protocols in a GMP laboratory setting with emphasis on attention to detail and accuracy of execution. * Documentation of results in accordance with cGMP * Comply with FDA, EPA and OSHA regulations, performing all work in a safe manner. * Reports lab testing data and completes documentation accurately and in accordance with laboratory procedures and regulatory requirements * Reviews results for conformance to standards * Perform analytical testing of pharmaceutical products following analytical methodology * Read and interpret analytical methodology and the USP * Supports method development and validation of new methods * Performs investigations and completes CAPA in response to deviations. * Develops and executes validation protocols for test methods and equipment qualification as requested. * Meet fundamental cGMP requirements relating to conduct and work practices to ensure the SISPQ (Safety, Identity, Strength, Purity, and Quality) of the all products manufactured/tested at Lonza Tampa. * Adhere to all defined Safety and Sustainability requirements and expectations and seek clarification whenever Safety and Sustainability requirements and expectations are either unknown or unclear * Promptly report identified Safety and Sustainability issues, problems, deficiencies, errors, incidents, and/or opportunities to management and correct where possible * Stop work where deemed necessary to maintain safety Key Requirement * Associate's Degree in Science, preferably chemistry * Minimum of 3 years experience in a GMP pharma environment * Actively participates in customer and regulatory audits * Demonstrated experience with peer review work and data of other analysts to ensure compliance with method and regulatory requirements Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Job Details Plant City, FL Full TimeDescription Armorock is a market leader of precast polymer concrete structures for the wastewater industry. Our mission is to drive the future of sustainable infrastructure with high-quality, innovative solutions that create lasting value. We are dedicated to exceeding customer expectations and fostering a collaborative, rewarding work environment through our QUESST core values: Quality, Unified, Efficient, Safe, Sustainable, Transparent. Position Overview The Quality Inspector is responsible for ensuring that all inventory stored within, and products produced by Armorock meet acceptable quality standards. Day-to-day responsibilities will include, but are not limited to inbound shipment review, outbound product inspection, data entry, report compilation, process observation, inventory review, safety and internal communication. Essential Duties and Responsibilities Service Delivery (80%) Perform pre-pour, post-pour, process, and final inspection of products. Initiate non-conformance reports. Perform receiving inspection and analysis of materials upon receipt. Assist QA Techs in the collection of quality data for analysis. Observe and support standardized manufacturing processes. Enter quality data into the database. Perform other related duties as assigned. Continuous Process Improvement (10%) Maintain SLAs and build a culture of continuous improvement Drive improvement in clarity of process flows and measurement across the organization Collaboration and Research (10%) Collaborate with corporate functions across the board to ensure any required changes to policies, procedures, and processes are implemented Collaborate with data owners/stewards to align on process and data issues Respond to questions and follow up on pertinent escalations Other Duties and Responsibilities Determines how to operationalize processes and improve production quality in alignment with strategic vision Utilizes knowledge of manufacturing operations to drive quality and consistency in operations Uses organizational skills and attention to detail; performs detailed work with speed and accuracy Demonstrates a positive attitude, energy and professionalism Leadership Core Competencies Execution: Sets own goals and ensures others in his/her team achieve goals aligned with business strategy. Building Working Relationships: Develops and builds partnerships with others inside or outside of the company who can provide support. Driving for Results: Sets challenging goals and objectives with clear purpose, direction, and outcomes. Innovation & Creativity: Builds creative solutions to customer and business needs. Essential Leadership Attributes Grounded: Connected to the values of the business; understands service to others/not about own ego. Operating Acumen: Understands varying business models and levers and can use them effectively to build key relationships. Agility/Flexibility: Adapts and executes during changing business conditions, processes, work cultures and environments. Authentic: Places the interests of others and the team ahead of his/her own self interests. Respects and values people and is comfortable living in his/her own skin. Qualifications Position Requirements Education: Bachelor's or associate degree in construction precast manufacturing Experience: 1-3 years' experience in Quality field Certification and Licenses: Familiarity with ISO 9000, NPCA or other certification requirements, preferred Travel Requirements: No major travel requirements Other Key Skills Ability to read blueprints. Ability to use tape measure and other metrology equipment to collect quality data Familiarity and ability to comply with standard quality assurance documentation and operations procedures. Computer literate and detail oriented Ability to work in a fast-paced environment with occasional overtime and weekend work Experience in pre-cast concrete or other heavy industry preferred Familiarity with ISO 9000, NPCA or other certification requirements, preferred Familiarity with lean manufacturing techniques ADA Requirements Environment (office or other): Onsite at manufacturing plant Equipment Operated: Computer, phone, forklift Lifting: Must be able to bend and lift heavy boxes Sitting: Must be able to remain standing and moving 50-75% of the time Management reserves the right to assign or reassign duties and responsibilities on this job at any time. Equal Opportunity Employer - Drug Free Workplace - Background Checks Conducted

Job DescriptionBenefits: Bonus based on performance Competitive salary Opportunity for advancement We are seeking a detail-oriented and dependable Field Quality Control Inspector to join our team. This role involves walking residential construction sites to ensure all work meets established quality standards and complies with client and regulatory requirements. The ideal candidate will have hands-on experience in construction inspections and a strong understanding of residential building practices. Key Responsibilities: Conduct daily field inspections at residential job sites to verify that work meets quality, safety, and compliance standards Inspect construction activities such as trenching, conduit installation, grounding, structural mounting, and equipment placement Ensure contractors adhere to approved specifications, codes, and client requirements Document inspection findings using detailed field notes, reports, and photo documentation Identify deficiencies or deviations and communicate corrective actions to the appropriate team Coordinate with project managers, subcontractors, and utility representatives to resolve issues in the field Ensure proper use and handling of materials and equipment on-site Maintain organized and up-to-date records of all inspections and communications Travel between job sites as required Qualifications: Previous experience in field inspection, construction, or utility-related work (OSP/telecom/electrical a plus) Strong understanding of residential construction processes and safety standards Ability to read and interpret construction drawings, site plans, and specifications Comfortable working outdoors and walking sites daily in various weather conditions Excellent communication and reporting skills Detail-oriented with a proactive approach to identifying and resolving issues Valid drivers license and reliable transportation Job Type: Full-time, Permanent (1099 Sub-Contractor) Pay: $21$25 per hour (based on experience) Expected Hours: 40 per week Schedule: 8-hour shift Day shift Monday to Friday Work Location: Field-based (on the road; residential job sites)

Forgen is dedicated to building a better future - for generations. The Quality Control Technician conducts daily inspections to ensure compliance with company and customer quality standards. They possess the authority to enforce corrective actions for any deficiencies in work, equipment, or materials. Their duties encompass maintaining quality assurance protocols, conducting material testing, and analyzing test results. They execute quality assessments, perform inspections, calibrate equipment, and communicate findings. Furthermore, they manage project document control, prepare submissions meeting project specifications and interpret plans to ensure project compliance. Forgen Overview Forgen is a leading geotechnical and specialty civil construction company operating across North America. We are dedicated to delivering innovative solutions for complex civil, geotechnical, and environmental challenges, guided by our core values of integrity, passion, teamwork, and smart work. Key Responsibilities This role will include temporary night shift periods. Inspecting the work in progress to assure compliance with the quality control plan and quality criteria as specified in the Contract Documents. Performing quality control sampling and testing during construction or ensuring that outside companies are performing tests according to the specifications. Verifying that the equipment used in testing meets test requirements, that tests are conducted according to procedures and best management practices, and that testing equipment and procedures remain consistent over the duration of the project. Identifying work that does not meet acceptance criteria, documenting defective work, and reporting to the QC Manager. Administering the Inspection Test Plans (ITP). Completing the daily field logs. Taking daily field photographs. Maintaining quality control document files. Inspect all delivered materials to document there are no defects in workmanship, they have the proper identification, are not damaged and delivery is complete. Visual inspection will also include the correct quantity, completeness evidence of compliance with approvals, and proper documentation in accordance with manufacturer's requirements and the contract documents. Monitor delivery, handling, and storage of materials per specifications. Observe that storage facilities are applicable, protective, and secure to prevent damage or contamination to equipment and materials per specifications. Review and maintain any manufacturer material certifications. Pertinent information will be entered, and any non-conformances identified during material inspections will be recorded on a Material Delivery Receipt. Basic Qualifications Degree in an engineering discipline (civil, mechanical, electrical, structural), preferred. Knowledge of mathematics - arithmetic, geometry, calculus, and statistics and their relevant applications. Computer skills especially in the use of Microsoft Word and PowerPoint and the ability to manage files and records effectively. Valid Driver's License and ability to drive on behalf of company business. Preferred Qualifications The following safety training is preferred, but not mandatory. Company will provide additional training, as necessary. 40-Hour HAZWOPER Training 8-Hour OSHA Refresher. Competent Person Safety Training. 30-Hour OSHA Construction Safety Training. EM 385-1-1 Training Physical Demands & Work Environment This role requires lifting up to 50 pounds, extended standing or walking on project sites, climbing in and out of equipment, and working in confined spaces or at heights. Work conditions and demands may vary, with possible exposure to heavy machinery, chemicals, dust, fumes, noise, and extreme weather. Proper PPE, including protective eyewear, gloves, a hard hat, and steel-toed boots, is required. Effective communication, tool use, and adherence to safety protocols are essential. This job description outlines the general scope of work and is not exhaustive. Employees may be assigned additional duties as needed. Requirements may be adjusted to accommodate disabilities, except where they pose a direct safety risk. Equal Opportunity Forgen is an equal-opportunity employer and prohibits discrimination based on any legally protected status. Privacy Policy At Forgen, we are committed to protecting your privacy. We collect and use your personal data to manage the recruitment process, including assessing your application, verifying information, and, if applicable, entering into an employment contract. Your information may be shared with authorized third parties who perform services on our behalf, such as background checks, and only where permitted by law. We implement appropriate security measures to safeguard your information and retain it only as long as necessary for recruitment and legal purposes. You have the right to access, correct, or request deletion of your data, and to withdraw your consent at any time where applicable. For questions or to exercise your rights, please contact *************. California Privacy Policy Agency Policy

Risk, Controls, and Assurance Intern- Summer 2026 Location: Tampa, FL. This role requires associates to be in-office 1 - 2 days per week, fostering collaboration and connectivity, while providing flexibility to support productivity and work-life balance. This approach combines structured office engagement with the autonomy of virtual work, promoting a dynamic and adaptable workplace. Please note that per our policy on hybrid/virtual work, candidates not within a reasonable commuting distance from the posting location(s) will not be considered for employment, unless an accommodation is granted as required by law. A Risk, Controls, and Assurance Intern will be responsible for supporting our Risk, Controls, and Assurance team in ensuring the stability and compliance of audit and regulatory requirements/mandates. Key regulations supported by these efforts include Sarbanes-Oxley (SOX), SOC1 reporting, SOC2 reporting, and the HiTrust Security certification. This position is a full-time, 12-week internship (May 18th, 2026 - August 7th, 2026) program in alignment with our Enterprise-wide Summer Internship program. How you will make an impact: Create and document results of control testing and review. Provide research support, develop work programs, engagement plans and collaborate with audit team members. Assess risk of IT systems, operational processes, and financial processes. Attend control walkthroughs with management and external auditors Assist with testing of IT General Controls Assist with process modernization (including but no limited to automation, AI, etc) Minimum Requirements: Actively pursuing a Bachelor's or Master's degree in either: Accounting, Business, Business Information Systems, Management Information Systems, or a related program or related degree at an accredited university or college The ability to work 40 hours per week for the duration of the internship and work in-office at least twice per week. Preferred Skills, Capabilities, and Experiences: Excellent Problem-solving, Analytical, and Organizational skills Excellent written and verbal communication skills Familiarity Microsoft Office Suite with emphasis on Excel and PowerPoint Comfortability and adaptability to thrive in a fast-paced environment An interest in health care and insurance Job Level: Non-Management Non-Exempt Workshift: Job Family: ADM > Intern Please be advised that Elevance Health only accepts resumes for compensation from agencies that have a signed agreement with Elevance Health. Any unsolicited resumes, including those submitted to hiring managers, are deemed to be the property of Elevance Health. Who We Are Elevance Health is a health company dedicated to improving lives and communities - and making healthcare simpler. We are a Fortune 25 company with a longstanding history in the healthcare industry, looking for leaders at all levels of the organization who are passionate about making an impact on our members and the communities we serve. How We Work At Elevance Health, we are creating a culture that is designed to advance our strategy but will also lead to personal and professional growth for our associates. Our values and behaviors are the root of our culture. They are how we achieve our strategy, power our business outcomes and drive our shared success - for our consumers, our associates, our communities and our business. We offer a range of market-competitive total rewards that include merit increases, paid holidays, Paid Time Off, and incentive bonus programs (unless covered by a collective bargaining agreement), medical, dental, vision, short and long term disability benefits, 401(k) +match, stock purchase plan, life insurance, wellness programs and financial education resources, to name a few. Elevance Health operates in a Hybrid Workforce Strategy. Unless specified as primarily virtual by the hiring manager, associates are required to work at an Elevance Health location at least once per week, and potentially several times per week. Specific requirements and expectations for time onsite will be discussed as part of the hiring process. The health of our associates and communities is a top priority for Elevance Health. We require all new candidates in certain patient/member-facing roles to become vaccinated against COVID-19 and Influenza. If you are not vaccinated, your offer will be rescinded unless you provide an acceptable explanation. Elevance Health will also follow all relevant federal, state and local laws. Elevance Health is an Equal Employment Opportunity employer, and all qualified applicants will receive consideration for employment without regard to age, citizenship status, color, creed, disability, ethnicity, genetic information, gender (including gender identity and gender expression), marital status, national origin, race, religion, sex, sexual orientation, veteran status or any other status or condition protected by applicable federal, state, or local laws. Applicants who require accommodation to participate in the job application process may contact ******************************************** for assistance. Qualified applicants with arrest or conviction records will be considered for employment in accordance with all federal, state, and local laws, including, but not limited to, the Los Angeles County Fair Chance Ordinance and the California Fair Chance Act.

Top Job Located in Temple Terrace, FL Salary: $18/hr Concrete Quality Control Tampa, FL Express Employment in Temple Terrace is currently hiring candidates for a Concrete Quality Control positionfor a local company. This position is full-time and has long-term opportunities. You will be responsible for testing, inspecting, and documenting the quality of concrete materials and finished products. Job Description: Pay rate $18 per hour Monday - Friday Long Term | First shift Perform routine testing of concrete materials, including slump, air content, temperature, and compressive strength Inspect precast concrete products for dimensional accuracy, surface finish, and structural integrity Maintain accurate records of test results and inspections Assist in troubleshooting quality issues and recommending corrective actions Ensure compliance with ASTM standards and project specifications Collaborate with production and engineering teams to uphold quality standards Qualifications and Requirements: Experience in concrete quality control preferred Bilingual in Spanish and English Strong attention to detail Ability to work outside in various weather conditions Recent and relevant work history in the last 6 months Any Questions: Call: 813-###-#### In office: 12814 N 56th St, Temple Terrace, FL, 33617 Express Employment Professionals offers competitive pay and benefits packages, including health insurance and weekly pay. If you meet the qualifications and are interested in this position, apply today! #3127FL Express Office: Tampa (Northeast) 12814 North 56th Street Tampa, FL 33617

Title: Quality Control Inspector Duration: 6 months (Possible extension) 1 PM TO 9 PM PAY RATE: $22/hR. Qualifications: 1 PM TO 9 PM Plans and directs activities concerned with development, application, and maintenance of quality standards for industrial processes, materials, and products. Tests and inspects products at various stages of the production process and compiles and evaluates statistical data to determine and maintain quality and reliability of products by performing the following duties. QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Must have Basic Computer Proficiency to include fundamental tasks such as email, word processing software, creating and maintaining spreadsheets in MS Excel and navigating Operating systems. EDUCATION and/or EXPERIENCE: Associate degree in an aviation related field preferred At least 1-year relevant aviation work experience Minimum of 2 years'experience in basic dimensional/visual inspection required on aviation related equipment (airframe, powerplant, and or avionic) Certify visual acuity to NAS-410 Airframe and Powerplant FAA certifications preferred Responsibilities: ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Provide quality control final inspection support, and shipping / receiving inspection support. Accurately interpret engineering drawings, customer specifications, company specifications, sampling procedures, designs, forms, and instructions for recording, evaluating, and reporting quality and reliability data. Utilize precision tools and equipment with accuracy for testing and measurement of products. Recommend modifications of existing quality or production standards to achieve optimum quality within limits of equipment capability.

The County Materials Family of Companies manufactures and delivers concrete construction products to meet the demand for growing communities. We rely on our talented and dedicated team members to provide reliable products with personalized service. We are seeking a Quality Control Technician for County Materials in Astatula, Florida Job Duties: * Performs quality control inspections, checks, and tests during the manufacture of products * Inspects materials, parts and products at different stages of production * Records observations and may make recommendations for improving processes * Familiar with standard concepts, practices, and procedures within the concrete industry * Regularly observes the production process including setup, casting, stripping and storage of product. * Work with production to identify and resolve quality issues related to casting and concrete performance. * Manage housekeeping to ensure a safe workplace. * Other tasks as needed Work Environment: * Work in indoor and outdoor weather conditions, including extreme hot or cold temperatures * Work near moving machinery and equipment - could include electrical hazards * Work in a noisy environment Physical Requirements: * Carrying/Lifting 10 - 40 Pounds frequently * Carrying/Lifting > 40 Pounds occasionally * Standing / Walking / Climbing * Squatting/Crouching/Kneeling/Bending * Pushing / Pulling / Reaching Above Shoulder Experience & Qualifications: * Understanding of a manufacturing environment. * Concrete plant and/or quality control experience highly desired. * Ability to interpret shop drawings and job specifications. * Proficient Computer Skills with Microsoft Office. * Solid math aptitude. * Must have the ability to train and obtain technical certifications as directed and supported by the company. * Ability to work independently. * Strong organizational, interpersonal and communication skills. * High School diploma or equivalency required. * 1-2 years prior experience in a manufacturing environment * Experience in the construction and/or building materials industry preferred, not required.

Are you looking to join Florida's fastest growing mechanical contracting team? B&I Contractors, Inc., a proud four-time winner of the Great Place to Work certification, is seeking an experienced and dedicated Commercial HVAC Piping Quality Control to join our dynamic and expanding team. Why Choose B&I Contractors, Inc.? * Industry Leader: As Florida's fastest growing mechanical contractor, we specialize in large-scale commercial projects. * Continuous Development: Benefit from our NCCER-certified in-house and online training that equips you with the skills needed to advance in your career. * Comprehensive Benefits: Enjoy employer-paid health insurance, accrued vacation, and sick time, along with a wellness reimbursement program to support your overall well-being. * Retirement Benefits: We are a 100% employee-owned company with an ESOP. You can also participate in our 401(k) plan with company match and explore post-tax Roth IRA options to secure your financial future. * Established Legacy: Join a team of over 1000 employees contributing to our success since 1960, with a proven track record of excellence in mechanical contracting. General Description: The Commercial Pipefitter Quality Assurance (QA) Representative is responsible for implementing and maintaining the quality management system for commercial piping projects. This role ensures that all quality standards and procedures are met and maintained on-site, with a focus on mechanical piping systems as well as air side equipment. The QA Representative coordinates with project stakeholders to guarantee compliance with quality objectives and industry standards such as ASME, ASTM, and local code requirements. Essential Functions: * Control and distribute all quality documentation for assigned piping projects. * Monitor and oversee all quality-related activities on the project, with a focus on plumbing and mechanical piping standards. * Attend client quality management meetings and represent the project's QA interests. * Prepare and maintain project-specific quality system documentation, including inspection and test plans (ITPs). * Oversee the disposition and resolution of nonconformance reports (NCRs) or rolling completion lists (RCL's). * Recommend and implement quality improvements based on field observations and audit findings in accordance with contract documents, plans, specs, and equipment manufacturers' recommendations. * Coordinate QA/QC activities with the Project Manager and Site Superintendent. * Maintain quality-related communication with customer representatives and inspectors. * Monitor and report statistical data related to quality performance and outcomes. * Address and resolve customer complaints related to piping quality and installation. * Archive all project documentation upon project completion in accordance with company procedures (ACC). * Perform light administrative duties to support the Project Superintendent. * Perform hands-on piping-related tasks at project sites as needed to verify installation quality and assist with inspections. Competencies: * Strong collaboration and communication skills. * Excellent organizational and problem-solving abilities. * Effective time management and task prioritization. * Proficiency in interpreting construction drawings and piping specifications. * Ability to review and understand submittals for piping materials, valves, and equipment. * Experience with Procore, ACC or similar construction management software. * Proficiency in using iPads or tablets for field reporting and documentation. * Ethical conduct and attention to detail. * Computer literacy and familiarity with QA/QC reporting tools. Physical Demands: This position requires the ability to lift and carry materials weighing up to 50 pounds on a frequent basis. The employee must be able to perform tasks involving physical labor, including lifting, pushing, pulling, and carrying materials, tools, or equipment. Manual material handling must be performed in accordance with OSHA safety standards and company policies to minimize risk of injury. Esta posición requiere la capacidad de levantar y transportar materiales de hasta 50 libras de manera frecuente. El empleado debe poder realizar tareas que involucren trabajo físico, incluyendo levantar, empujar, jalar y transportar materiales, herramientas o equipo. El manejo manual de materiales debe realizarse de acuerdo con los estándares de seguridad de OSHA y las políticas de la compañía para minimizar el riesgo de lesiones. Required Education and Experience: * 8+ years of field experience in commercial piping systems. * Proficiency in reading and interpreting blueprints, drawings, and piping specifications. * Strong problem-solving skills, especially with layout and installation concepts. * Proficiency in basic math and ability to perform relevant calculations. #bandi1

THIS IS A TEMPORARY EMPLOYMENT OPPORTUNITY MLU Services LLC is looking for a HVAC Quality Control Maintenance Inspector to join our team. The successful candidate will be responsible for performing maintenance and repairs on trailers. The ideal candidate will have experience working with mobile homes and travel trailers. Job Duties and Responsibilities include: Perform routine maintenance on mobile homes and travel trailers Knowledge in working with water, sewer, and electrical Ensure all work is completed in a timely and efficient manner Maintain accurate records of all work performed Communicate with customers regarding repairs and maintenance Adhere to all safety protocols and guidelines Skills and Competencies: Strong knowledge of mobile homes and travel trailers Ability to diagnose and troubleshoot issues quickly and efficiently Ability to work independently and as part of a team Education and Experience: High school diploma or equivalent preferred 2 years of experience working as an HVAC Technician preferred Valid driver's license Professional communication skills both verbal & written Desired Certification OSHA 30 (General Industry or Construction Safety) OSHA 10 (General Industry or Construction Safety) Physical Demands: Ability to lift over 50+ pounds Ability to stand, bend, and kneel for extended periods of time Ability to work in a variety of weather conditions Job Description Disclaimer This position description incorporates the job's core responsibilities. It recognizes that other related duties not specifically mentioned might also be performed and that not all responsibilities may be carried out depending on operational needs. All qualified applicants will receive consideration for employment without regard to race, color, religion, sexual orientation, national origin, disability, or status as a protected veteran. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the position. Upon hire, secondary employment and other employment restrictions must be disclosed and approved. Tidal Basin Holdco, LLC, and its subsidiaries and affiliated companies, are an Equal Employment Opportunity Employer.

The Quality Assurance (QA) Microbiologist plays a pivotal role in upholding our product quality standards by actively supporting the Quality Management System. This position primarily focuses on investigating the growth, potential sources, and specific attributes of microscopic organisms within Treatt products. The QA Microbiologist collaborates closely with the Quality Assurance Supervisor and cross-functional teams to ensure product safety and quality compliance. The duties and tasks of the Quality Assurance (QA) Microbiologist involve the following: Oversee and maintain the Retain Program to ensure proper storage and organization of retained samples for future reference. Manage and maintain the ATP Program, including the weekly calibration of ATP equipment, to ensure accurate and consistent results. Send monthly trending report to QA Supervisor. Manage and maintain the Environmental Program, which includes monitoring and maintaining cleanliness and hygiene within the production environment. Send monthly trending report to QA Supervisor. Administer and maintain weekly water analysis to verify the quality and safety of water sources. Send monthly trending report to QA Supervisor. Manage and maintain the Temperature Monitoring Program, ensuring temperature controls are in place and documented as per quality standards. Review and report on area cleaning logs weekly. Assist in conducting daily walkthroughs and reporting findings. Manage and maintain the Glass and Knife Programs Assist in investigating and consulting microbiological complaints and CAPAs to resolve quality issues effectively. Provide necessary training to operators on plant hygiene as needed to uphold cleanliness and microbiological safety standards. Conduct validation studies related to environmental and equipment testing, ensuring the reliability of our quality control processes. Actively contribute as a member of the internal audit team, ensuring timely completion of internal audits and adherence to compliance standards. Participate as a key member of the HACCP team, supporting the implementation and maintenance of food safety protocols. Support the QA Supervisor in the implementation of corrective action plans pertaining to microbiological concerns identified during audits. Assist in investigating Soleris anomalies as requested by the QA Supervisor or QC Manager to maintain product quality and safety. Analyze and interpret microbiological data as requested by the QA Supervisor or QC Manager to identify trends and areas for improvement. Provide consultation on laboratory equipment upgrades, as requested by the QC Manager, to enhance testing and analysis capabilities. Collaborate with the Innovation team to assess potential microbiological contamination risks in new product developments and offer guidance on risk mitigation strategies. Assist with microbiological training as needed for new laboratory hires or during method/equipment changes as requested by QC Manager. Undertake any other tasks that align with the overall job description and contribute to the quality and safety of our products. EDUCATION: Bachelor's or MS degree in Microbiology or Food Science, or related, from an accredited college or university. Previous experience of working in a microbiological laboratory and knowledge of quality assurance, preferred. A track record of successful teamwork in a manufacturing environment. Knowledge of HACCP, GMP, food safety, and related food safety regulations and processes is preferred. KNOWLEDGE AND EXPERIENCE: A minimum of 2-4 years of relevant work experience, with an understanding of food safety and regulations. Proficiency in Microsoft Office is required. Familiarity with ERP systems like SAP or JD Edwards is preferred.

Job Title: QC Chemist Ready to make an impact? Join Lonza Tampa as a QC Chemist and help ensure the quality and safety of life-changing medicines. In this role, you'll work in a cutting-edge GMP laboratory, collaborating with passionate professionals to deliver products that improve lives worldwide. What you will get An agile career and dynamic working culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. Medical, dental, and vision insurance. Our full list of global benefits can be found here: *************************************** What you will do Perform analytical testing of raw materials, in-process items, and finished products in a GMP laboratory setting. Document results accurately in compliance with cGMP and regulatory standards. Review data for conformance to specifications and report findings promptly. Support method development, validation, and equipment qualification activities. Investigate deviations and implement corrective and preventive actions (CAPA). Ensure adherence to FDA, EPA, and OSHA regulations while maintaining safety and sustainability standards. Contribute to maintaining product Safety, Identity, Strength, Purity, and Quality (SISPQ). What we are looking for Associate's Degree in Science, preferably Chemistry required. Minimum of 3 years' experience in a GMP pharmaceutical environment required. Proficient in HPLC techniques, including hands-on experience with Empower software required. Familiarity with Solutia systems or similar platforms required. Strong knowledge of analytical methodologies and USP standards. Ability to review peer data for compliance with regulatory requirements. Experience supporting audits and regulatory inspections. Detail-oriented with strong documentation and problem-solving skills. Commitment to safety and quality in all work practices. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now

Job Title: QC Chemist Ready to make an impact? Join Lonza Tampa as a QC Chemist and help ensure the quality and safety of life-changing medicines. In this role, you'll work in a cutting-edge GMP laboratory, collaborating with passionate professionals to deliver products that improve lives worldwide. What you will get * An agile career and dynamic working culture. * An inclusive and ethical workplace. * Compensation programs that recognize high performance. * Medical, dental, and vision insurance. * Our full list of global benefits can be found here: *************************************** What you will do * Perform analytical testing of raw materials, in-process items, and finished products in a GMP laboratory setting. * Document results accurately in compliance with cGMP and regulatory standards. * Review data for conformance to specifications and report findings promptly. * Support method development, validation, and equipment qualification activities. * Investigate deviations and implement corrective and preventive actions (CAPA). * Ensure adherence to FDA, EPA, and OSHA regulations while maintaining safety and sustainability standards. * Contribute to maintaining product Safety, Identity, Strength, Purity, and Quality (SISPQ). What we are looking for * Associate's Degree in Science, preferably Chemistry required. * Minimum of 3 years' experience in a GMP pharmaceutical environment required. * Proficient in HPLC techniques, including hands-on experience with Empower software required. * Familiarity with Solutia systems or similar platforms required. * Strong knowledge of analytical methodologies and USP standards. * Ability to review peer data for compliance with regulatory requirements. * Experience supporting audits and regulatory inspections. * Detail-oriented with strong documentation and problem-solving skills. * Commitment to safety and quality in all work practices. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now