{"schemaVersion":"jobsearcher.job.v1","id":"0450e883dded1f9209b7ff14","url":"https://jobsearcher.com/jobs/0450e883dded1f9209b7ff14","canonicalUrl":"https://jobsearcher.com/jobs/0450e883dded1f9209b7ff14","title":"Quality Control Manager","description":"PL Developments, also known as PLD, is a leading manufacturer, packager, and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goodsSummaryThe Quality Control (QC) Manager is responsible for leading and managing Quality Control laboratory operations to ensure the timely testing, release, and compliance of raw materials, in-process materials, bulk, stability, and finished products. This role ensures adherence to current Good Manufacturing Practices (cGMP), FDA regulations, and company quality standards while providing strong leadership, technical expertise, and continuous improvement within the QC function.Work schedule: Monday- Friday 8am-5pmJob QualificationsBachelor’s or Master’s Degree in Chemistry, Biology, or a related scientific disciplineMinimum of 7 years of experience in a Quality Control laboratory environment within a regulated industry (pharmaceutical, biotech, or related)Strong working knowledge of cGMPs, FDA regulations, and FDA guidance documentsDemonstrated leadership and people management experienceProven ability to plan, organize, and manage multiple priorities and projects simultaneouslyStrong attention to detail with consistent focus on data integrity and complianceAbility to work effectively in a fast-paced, matrixed environment, both independently and as part of a teamExcellent verbal, written, and interpersonal communication skillsComputer proficiency, including experience with laboratory systems and standard office softwarePosition ResponsibilitiesDirectly supervise and provide leadership to QC laboratory technical and support staffManage the development, implementation, and continuous improvement of QC goals, objectives, procedures, and systems in alignment with company policies and cGMP requirementsEstablish, review, and maintain analytical procedures, methods, and testing guidelinesEstablish and maintain testing schedule to assure adherence to Quality On Time Release (OTR), including Raw Materials, In-Process, Finished Product and StabilityRecruit, train, coach, and develop QC staff; assign work, monitor performance, and conduct performance evaluationsPerform or oversee analytical testing, data review, and approval activities as neededOversee raw material testing, in-process testing, bulk testing, stability testing, and finished product testingSupervise and participate in stability programs, method transfers, and analytical method validationsEnsure the development, review, approval, and maintenance of Certificates of Analysis for bulk and finished productsOversee the laboratory equipment qualification, calibration, and maintenance programsLead laboratory investigations, deviations, OOS/OOT investigations, and recommend corrective and preventive actions (CAPAs)Develop, review, and maintain Quality Control Standard Operating Procedures (SOPs)Support internal and external audits, inspections, and regulatory agency interactions as requiredPartner cross-functionally with Quality Assurance, Manufacturing, R&D, and other departments to support product quality and continuous improvement initiativesPerform additional duties as assigned by the Head of QualityEnsure QC Laboratory compliance with 21 CFR 210 & 211 and Part 11Lead as an QC SME for Internal, Client and Regulatory Audits as neededPhyisical RequirementsAdhere to all safety policies, including the use of personal protective equipment when requiredLight physical activity performing non-strenuous administrative and laboratory dutiesSitting for greater than 75% of the workday; standing and walking up to 25%Manual dexterity sufficient for handling laboratory equipment, samples, and computer workUse of hands and fingers for typing and laboratory tasks up to 75% of the timeOccasional reaching, bending, kneeling, crouching, or climbing less than 25% of the timeAbility to lift up to 50 pounds less than 25% of the timeBenefitsPLD is a proud employer offering many corporate benefits, including: Medical and Dental Benefits Vision 401K with employer match Group Life Insurance Flex Spending Accounts Paid Time Off and Paid Holidays Tuition Assistance Corporate Discount Program Opportunities to Flourish Within the CompanyPL Developments is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.#HP1","company":"Pl Developments","rawCompany":"pl developments","city":"Miami","state":"FL","isRemote":false,"isActive":false,"createdAt":"2026-05-03T02:52:04.067Z","occupations":[{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"11-9121.00","title":"Natural Sciences Managers","slug":"natural-sciences-managers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325998","title":"All Other Miscellaneous Chemical Product and Preparation Manufacturing","slug":"all-other-miscellaneous-chemical-product-and-preparation-manufacturing"},{"code":"541380","title":"Testing Laboratories and Services","slug":"testing-laboratories-and-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Quality Control Manager","description":"PL Developments, also known as PLD, is a leading manufacturer, packager, and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goodsSummaryThe Quality Control (QC) Manager is responsible for leading and managing Quality Control laboratory operations to ensure the timely testing, release, and compliance of raw materials, in-process materials, bulk, stability, and finished products. This role ensures adherence to current Good Manufacturing Practices (cGMP), FDA regulations, and company quality standards while providing strong leadership, technical expertise, and continuous improvement within the QC function.Work schedule: Monday- Friday 8am-5pmJob QualificationsBachelor’s or Master’s Degree in Chemistry, Biology, or a related scientific disciplineMinimum of 7 years of experience in a Quality Control laboratory environment within a regulated industry (pharmaceutical, biotech, or related)Strong working knowledge of cGMPs, FDA regulations, and FDA guidance documentsDemonstrated leadership and people management experienceProven ability to plan, organize, and manage multiple priorities and projects simultaneouslyStrong attention to detail with consistent focus on data integrity and complianceAbility to work effectively in a fast-paced, matrixed environment, both independently and as part of a teamExcellent verbal, written, and interpersonal communication skillsComputer proficiency, including experience with laboratory systems and standard office softwarePosition ResponsibilitiesDirectly supervise and provide leadership to QC laboratory technical and support staffManage the development, implementation, and continuous improvement of QC goals, objectives, procedures, and systems in alignment with company policies and cGMP requirementsEstablish, review, and maintain analytical procedures, methods, and testing guidelinesEstablish and maintain testing schedule to assure adherence to Quality On Time Release (OTR), including Raw Materials, In-Process, Finished Product and StabilityRecruit, train, coach, and develop QC staff; assign work, monitor performance, and conduct performance evaluationsPerform or oversee analytical testing, data review, and approval activities as neededOversee raw material testing, in-process testing, bulk testing, stability testing, and finished product testingSupervise and participate in stability programs, method transfers, and analytical method validationsEnsure the development, review, approval, and maintenance of Certificates of Analysis for bulk and finished productsOversee the laboratory equipment qualification, calibration, and maintenance programsLead laboratory investigations, deviations, OOS/OOT investigations, and recommend corrective and preventive actions (CAPAs)Develop, review, and maintain Quality Control Standard Operating Procedures (SOPs)Support internal and external audits, inspections, and regulatory agency interactions as requiredPartner cross-functionally with Quality Assurance, Manufacturing, R&D, and other departments to support product quality and continuous improvement initiativesPerform additional duties as assigned by the Head of QualityEnsure QC Laboratory compliance with 21 CFR 210 & 211 and Part 11Lead as an QC SME for Internal, Client and Regulatory Audits as neededPhyisical RequirementsAdhere to all safety policies, including the use of personal protective equipment when requiredLight physical activity performing non-strenuous administrative and laboratory dutiesSitting for greater than 75% of the workday; standing and walking up to 25%Manual dexterity sufficient for handling laboratory equipment, samples, and computer workUse of hands and fingers for typing and laboratory tasks up to 75% of the timeOccasional reaching, bending, kneeling, crouching, or climbing less than 25% of the timeAbility to lift up to 50 pounds less than 25% of the timeBenefitsPLD is a proud employer offering many corporate benefits, including: Medical and Dental Benefits Vision 401K with employer match Group Life Insurance Flex Spending Accounts Paid Time Off and Paid Holidays Tuition Assistance Corporate Discount Program Opportunities to Flourish Within the CompanyPL Developments is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.#HP1","datePosted":"2026-05-03T02:52:04.067Z","dateModified":"2026-05-03T02:52:04.067Z","hiringOrganization":{"@type":"Organization","name":"Pl Developments","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Miami","addressRegion":"FL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"0450e883dded1f9209b7ff14"},"url":"https://jobsearcher.com/jobs/0450e883dded1f9209b7ff14"}}