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
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...Responsibilities include leading cross-functional teams to support design and supplier changes, CAPAs, NCRs, Product Complaints and other compliance... ...on design changes, process improvement projects and quality/compliance initiatives.Creates and executes protocols for...QualitySeniorWork at officeWorldwideFlexible hours- ...impact. The Impact That You Will Make The Sr. Buyer is critical to the evolution of... ...requests, placing orders, tracking status, supplier follow up, invoice reconciliation and order... ...relationship with Operations Support, Quality Assurance, Quality Control, Project Management...QualitySeniorContract workShift work
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$115k - $130k
...transformative transportation initiatives that enhance safety, mobility, and quality of life across communities throughout the Northeast. This is a... ...guidance to junior engineers and technicians, including QA/QC reviews to uphold quality standards.Support business...QualitySeniorLocal areaFlexible hours$57.4k - $99k
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...Enterprise Application Development, Integration Development, Leadership, Problem Solving, Process Improvements, Product Development, Project Management, Quality Assurance (QA), Software Development, System Designs, Technical Support, Troubleshooting, Workday FinancialsQualitySeniorRemote workHome office£60k per year
...the UK's largest independent provider of specialist education and care. Through our... ...programmes involving multiple stakeholders, suppliers and technical teams, ensuring projects are... ...compliance requirements. Ability to produce high‑quality reporting and presentations for senior...QualitySeniorPermanent employmentFull timeContract workWork at officeLocal areaMonday to FridayFlexible hours2 days per week$80k - $90k
...ConsultingCompany OverviewWe are a leading environmental testing and consulting firm specializing in asbestos, mold, lead, indoor air quality and building science assessments. We help our clients identify, assess and resolve environmental hazards through expert...QualitySenior- ...goodwill impairments, ESOP valuations, estate and gifting, and minority shareholder matters.Manage engagements end-to-end, ensuring quality, accuracy, and timely delivery.Present findings to executive teams, boards, attorneys, and advisors with clarity and confidence.Act...QualitySeniorWork at officeLocal area
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