Sr. QA Specialist - Supplier Quality
PCI Pharma Services
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.We are PCI. Our 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.JOB DESCRIPTION:Position Title: Sr. QA Specialist – Supplier QualityLocation: Bedford, New HampshireDepartment: Quality AssuranceReporting To: QA Dir, Quality Systems & ComplianceResponsible For (Staff): NoThis position is part of PCI’s Quality Compliance team responsible for the quality aspects of supplier quality management for suppliers that provide raw materials, components, contract test labs and services for GMP operations. The position is responsible to ensure all aspects of the Supplier Qualification program are successfully executed across all PCI facilities.ESSENTIAL DUTIES AND RESPONSIBILITIES:Responsible for compliance relative to the overall Supplier Qualification Program by performing supplier audits to evaluate compliance to standard operating procedures, quality and regulatory standards and is responsible for creating and issuance of audit reportsResponsible for follow up and tracking of supplier audit observations to assure timely closureMonitor and communicate supplier change notifications and manage supplier non-conformance and complaint handlingResponsible for reviewing all audit responses to assure non-recurrence of deficienciesMaintain, trend, analyze and report quality metrics as it relates to supplier audits and performanceDrafting, review and management of supplier quality assurance agreements (QAA’s) and non-disclosure agreementsProvide support for Quality Council meetingsProvides support during FDA and other regulatory agency inspectionsComplete assignments and works independently without appreciable directionWrites and revises QA Standard Operating Procedures (SOP)Support continuous improvement initiativesPerforms other duties as assigned.QUALIFICATIONS:Required:Bachelor of Science Degree preferred with 15+ years’ in a QA GMP environment; alternatively, Master’s Degree with 10+ years’ experience in a QA GMP environment. (High School diploma with 20+ years’ of progressive experience in QA GMP environment).Exceptional organizational skillsExcellent interpersonal skills and the ability to communicate well orally and in writingProficiency in MS Office including Word, Excel, Access and VisioExcellent verbal and written communication skills requiredExperience with GMP quality systems in a pharmaceutical/biotech/medical device environment is a mustThorough knowledge of FDA regulations (i.e., 21CFR Part 210, 211 & 820) Guidance’s, and ICH is required; EMEA and other agency regulationsPreferred:Auditing certification preferred (i.e., ASQ, CQA or similar)Experience working with cross-functional teams, including giving training and/or presentations to large groupsDetail oriented and a results driven team playerAbility to work in a dynamic, fast paced work environmentHonesty, integrity, respect and courtesy with all colleagues Creative with the ability to work with minimal supervision and balanced with independent thinkingResilient through operational and organizational change#LI-RS1Join us and be part of building the bridge between life changing therapies and patients. Let’s talk futureEqual Employment Opportunity (EEO) Statement:PCI 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.At 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.SummaryLocation: Bedford, NH, USAType: Full time
- ...the future of PCI.This position is part of PCI’s Quality Compliance team responsible for the quality aspects of supplier quality management for suppliers that provide... ...of Science Degree preferred with 3+ years’ in a QA GMP environment; High School diploma with 5+ years...QualityFull timeContract work
$95k - $124k
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Department: 107100 Quality Location: San Diego, USA- Remote Be a... ...Position Summary The Senior Specialist, Quality Assurance Technical,... ...Change Controls related to supplier changes Manufacturing and Laboratory... ...job performance. Support QA with various technical...QualitySeniorContract workTemporary workInterim roleRemote work- Position Summary The Sr. Quality Inspector is a senior role within the quality team, responsible for overseeing inspections, mentoring junior inspectors, and ensuring all products meet or exceed regulatory and customer requirements. This position involves leading inspections...QualitySeniorContract workWork experience placementWork at office
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- ...Senior CAD Designer contributes design modifications to improve the quality and function of the product and may be responsible for the... ...other documented information furnished by Design Engineers or from suppliers. Creating drawings by planning arrangement of a product...QualitySenior
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- ...our global network to pioneer and shape the future of PCI.Position Title: QA Operations Specialist I - Floor SupportLocation: Bedford, New HampshireDepartment: Quality Assurance,Reporting To: Sr. Director, QualityResponsible For (Staff): NoThe QA Operations Specialist...QualityFull timeImmediate startFlexible hoursShift work
- ...impact. The Impact That You Will MakeThe Sr. Buyer is critical to the evolution of ARMI... ..., placing orders, tracking status, supplier follow up, invoice reconciliation and order... ...seamless relationship with Operations Support, Quality Assurance, Quality Control, Project...QualitySeniorContract workShift work
- ...behalf of Millyard Advanced Medical Products, is looking for a Quality Systems Specialis t to work in a dynamic Medical Device Research... ...training as required to DEKA personnel Promote QMS awareness to non-QA departments throughout DEKA Skills needed to be successful: 2+...QualityContract workWork at office
$88k - $132k
...Accounting teams. This role partners closely with IT to ensure data quality, integrity, and seamless integration across Salesforce CPQ,... ...implement solutions Participate in all stages of the SDLC, including QA and UAT, for Zuora-related changes and dependent system impacts...QualitySeniorRemote workHome office$159.43k
...make a difference and change the world. Job Description Job Duties: • Develop, implement, and maintain the project-specific Quality Assurance Surveillance Plan (QASP) in compliance with Federal Acquisition Regulations (FAR), Construction Quality Management (CQM)...QualityContract workFor contractorsWork experience placementFor subcontractorH1bImmediate startFlexible hours- DEKA Research & Development in Manchester, NH, seeks a Quality Systems Specialist to maintain and improve the quality management system in a dynamic medical device R&D setting. This high visibility role reports to the Director of Quality and directly impacts quality records...Quality
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