Ourvita · 11 hours ago
Quality Control Manager
Largo, FL
Full-time
Onsite
Senior Level
7+ years expOurvita is the largest Europe-based CDMO for food supplements, with a strong global presence. The Quality Control (QC) Manager is responsible for overseeing all aspects of the Quality Control laboratory, ensuring compliance with cGMP and regulatory standards while providing leadership and technical expertise.
CosmeticsManufacturingMedical Device
Responsibilities
Manage day-to-day operations of QC laboratories (Analytical and Micro) to ensure timely and accurate testing
Schedule QC team members and resources to meet organizational commitments
Ensure compliance with GMPs, SOPs, and regulatory requirements (21 CFR 111/211, NSF, FDA, etc.)
Oversee incoming material inspections, sampling, and disposition of components and finished products
Develop, validate, and maintain test methods and specifications for raw materials and finished products
Review and approve technical reports, SOPs, protocols, and laboratory documentation
Investigate and document deviations, OOS results, and implement CAPAs
Manage stability programs and ensure timely reporting
Ensure accuracy and integrity of all QC data, review data for compliance with specifications. Represents QC in cross-functional project teams and client interactions
Identify and implement process improvements and best practices
Support internal and external audits and regulatory inspections
Supervise day-to-day operations of assigned team or workgroups to ensure organizational and objectives are met
Understand and adhere to Good Manufacturing Practices
Stop any observed unsafe acts and obey facility safety rules and procedures
Correct or report any observed safety hazards
Support safety policies and programs
Provides leadership and direction to the Quality Control (QC) team
Carries out supervisory responsibilities in accordance with the organization’s policies and applicable laws
Interviews, hires, and trains employees; plans, assigns, and directs work; appraises performance; rewards and disciplines employees; addresses complaints and resolves problems
Qualification
Required
Bachelor's degree or higher in Chemistry or related scientific field
Minimum 7–10 years of experience in QC operations within pharmaceutical, food, or dietary supplement industry
Minimum 5 years of supervisory/management experience in a cGMP laboratory environment
Capable of interaction at all levels of the organization
Strong leadership and team development skills
Excellent technical knowledge of analytical chemistry and microbiology
Proficiency with analytical techniques and instruments: HPLC/UPLC, GC, LC-MS/MS, ICP-MS, KF, UV/Vis, FTIR
Familiarity with compendial standards (USP, FCC, AOAC)
Strong organizational, problem-solving, and communication skills
Ability to manage multiple projects and meet deadlines
Computer proficiency (MS Word, Excel, PowerPoint, Outlook, Access)
Experience supporting regulatory and third-party audits
Benefits
Medical, Dental, and Vision coverage
Basic Life, Accidental Death and Dismemberment (AD&D), Short Term Disability (STD) and Long-Term Disability (LTD) benefits at no cost to employees
Retirement Plan 401(k) match
Holiday pay and Paid Time Off (PTO)
Opportunities for advancement
Fitness discounts
Tuition Reimbursement
Company
Ourvita
Ourvita innovates and manufactures health supplements, medical equipment, and wellness goods.
1001-5000 employees
Funding
Current Stage
Late StageCompany data provided by crunchbase