{"schemaVersion":"jobsearcher.job.v1","id":"923feb5bbe93671ca2e00aae","url":"https://jobsearcher.com/jobs/923feb5bbe93671ca2e00aae","canonicalUrl":"https://jobsearcher.com/jobs/923feb5bbe93671ca2e00aae","title":"Supervisor, QA Internal Operations","description":"Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.\n\nWe are PCI.\n\nOur investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.\n\nJOB DESCRIPTION:\n\nPosition Title: Supervisor, QA Internal Operations\n\nLocation: Bedford, NH\n\nDepartment: Quality Assurance Internal Operations\n\nReporting To: Senior Manager QA Operations\n\nResponsible For (Staff): Yes\n\nThe Supervisor, QA Internal Operations is responsible for leading a team of QA Operations Associates responsible for on-the- floor support (Quality in Plant –or QIP) that provides 7 days a week QA oversight. This includes providing QA support in the manufacturing of clinical and commercial drug products/medical devices to ensure compliance with the principles and guidelines of cGMP. The QA Supervisor assists in assisting with quality systems, such as laboratory control, investigation management, materials management, document control and training to ensure control of the manufacturing process. This position will actively partner with Manufacturing Operations, Visual Inspection, Materials Management, and other supporting departments to provide compliance and technical guidance to ensure quality issues are identified and resolved in a timely manner.\n\nESSENTIAL DUTIES AND RESPONSIBILITIES:\n\nOversee and provide QA support and guidance for daily cGMP manufacturing operations.\nCoordinate with cross-functional teams to continually improve procedures with respect to area line clearances, labeling, packaging and material release.\nSupport scheduling activities by monitoring the production and visual inspection schedules and reviewing factors that may impact schedules.\nOversee and assist employees with product / material labeling and disposition functions, routine manufacturing area line clearances; Assist with AQL Sampling and Inspection of Final Package Lots.\nReview and approval of Blue Mountain documents and work orders\nComplete staff performance reviews and align personnel goals to corporate initiatives.\nEnsure all pertinent training is assigned to staff, and employee training is in good standing\nAssist with review of master and executed raw material records and logbooks\nReview of associated QC data to support facility and products\nParticipation in writing or revising Standard Operating Procedures, material control procedures, deviations, CAPA’s, and Quality Investigations when applicable.\nSupport external client audits at LSNE, and regulatory inspections\nObtain gown qualification for sterile manufacturing line clears\nMaintain and evaluate current processes and procedures, and look for opportunities for continuous improvement\nOther duties as assigned\nGuide personnel indirectly and directly involved in GMP operations pertaining to cGMP compliance, internal procedures, regulatory requirements and industry best practices\n\nAssist QA Specialists in batch record reviews and generating CoAs\n\nQUALIFICATIONS:\n\nRequired:\n\nBachelor’s Degree in relevant scientific discipline\n5+ years of pharmaceutical or biotech industry experience\n3+ years of experience in a QA Operations role supporting late stage clinical and/or commercial production, or equivalent.\nASQ certification Highly preferred\nExceptional organizational skills and attention to detail\nAbility to make risk based decisions and resolve issues with minimal guidance\nExcellent interpersonal skills and the ability to communicate well orally and in writing\nProficiency in MS Office including Word, and Excel\nExcellent verbal and written communication skills required\n\nPreferred:\n\nAbility to supervise and lead people in a dynamic, fast paced work environment\nHonesty, integrity, respect and courtesy with all colleagues\nCreative with the ability to work with minimal supervision and balanced with independent thinking\nResilient through operational and organizational change\nAbility to coach, train, and mentor others\nCross functional staff, members of management, internal and external clients, members of the Quality organization\n\n#LI-RS1\n\nJoin us and be part of building the bridge between life changing therapies and patients. Let’s talk future\n\nEqual Employment Opportunity (EEO) Statement:\nPCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.\n\nAt PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.","company":"Pcipharmaservices","rawCompany":"pcipharmaservices","city":"Bedford","state":"NH","isRemote":false,"isActive":false,"createdAt":"2026-08-19T21:04:43.485Z","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":"51-1011.00","title":"First-Line Supervisors of Production and Operating Workers","slug":"first-line-supervisors-of-production-and-operating-workers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Supervisor, QA Internal Operations","description":"Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.\n\nWe are PCI.\n\nOur investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.\n\nJOB DESCRIPTION:\n\nPosition Title: Supervisor, QA Internal Operations\n\nLocation: Bedford, NH\n\nDepartment: Quality Assurance Internal Operations\n\nReporting To: Senior Manager QA Operations\n\nResponsible For (Staff): Yes\n\nThe Supervisor, QA Internal Operations is responsible for leading a team of QA Operations Associates responsible for on-the- floor support (Quality in Plant –or QIP) that provides 7 days a week QA oversight. This includes providing QA support in the manufacturing of clinical and commercial drug products/medical devices to ensure compliance with the principles and guidelines of cGMP. The QA Supervisor assists in assisting with quality systems, such as laboratory control, investigation management, materials management, document control and training to ensure control of the manufacturing process. This position will actively partner with Manufacturing Operations, Visual Inspection, Materials Management, and other supporting departments to provide compliance and technical guidance to ensure quality issues are identified and resolved in a timely manner.\n\nESSENTIAL DUTIES AND RESPONSIBILITIES:\n\nOversee and provide QA support and guidance for daily cGMP manufacturing operations.\nCoordinate with cross-functional teams to continually improve procedures with respect to area line clearances, labeling, packaging and material release.\nSupport scheduling activities by monitoring the production and visual inspection schedules and reviewing factors that may impact schedules.\nOversee and assist employees with product / material labeling and disposition functions, routine manufacturing area line clearances; Assist with AQL Sampling and Inspection of Final Package Lots.\nReview and approval of Blue Mountain documents and work orders\nComplete staff performance reviews and align personnel goals to corporate initiatives.\nEnsure all pertinent training is assigned to staff, and employee training is in good standing\nAssist with review of master and executed raw material records and logbooks\nReview of associated QC data to support facility and products\nParticipation in writing or revising Standard Operating Procedures, material control procedures, deviations, CAPA’s, and Quality Investigations when applicable.\nSupport external client audits at LSNE, and regulatory inspections\nObtain gown qualification for sterile manufacturing line clears\nMaintain and evaluate current processes and procedures, and look for opportunities for continuous improvement\nOther duties as assigned\nGuide personnel indirectly and directly involved in GMP operations pertaining to cGMP compliance, internal procedures, regulatory requirements and industry best practices\n\nAssist QA Specialists in batch record reviews and generating CoAs\n\nQUALIFICATIONS:\n\nRequired:\n\nBachelor’s Degree in relevant scientific discipline\n5+ years of pharmaceutical or biotech industry experience\n3+ years of experience in a QA Operations role supporting late stage clinical and/or commercial production, or equivalent.\nASQ certification Highly preferred\nExceptional organizational skills and attention to detail\nAbility to make risk based decisions and resolve issues with minimal guidance\nExcellent interpersonal skills and the ability to communicate well orally and in writing\nProficiency in MS Office including Word, and Excel\nExcellent verbal and written communication skills required\n\nPreferred:\n\nAbility to supervise and lead people in a dynamic, fast paced work environment\nHonesty, integrity, respect and courtesy with all colleagues\nCreative with the ability to work with minimal supervision and balanced with independent thinking\nResilient through operational and organizational change\nAbility to coach, train, and mentor others\nCross functional staff, members of management, internal and external clients, members of the Quality organization\n\n#LI-RS1\n\nJoin us and be part of building the bridge between life changing therapies and patients. Let’s talk future\n\nEqual Employment Opportunity (EEO) Statement:\nPCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.\n\nAt PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.","datePosted":"2026-08-19T21:04:43.485Z","dateModified":"2026-08-19T21:04:43.485Z","hiringOrganization":{"@type":"Organization","name":"Pcipharmaservices","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bedford","addressRegion":"NH","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"923feb5bbe93671ca2e00aae"},"url":"https://jobsearcher.com/jobs/923feb5bbe93671ca2e00aae"}}