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.Responsibilities:
Perform functions following quality criteria, safety, and health standards.Carry out job duties aligned with the company's established behavioral values.Work according to GMP regulations.Perform tasks related to quality assurance, including quality inspection responsibilities.Collaborate to maintain order and cleanliness in the area.Conduct AQL inspections of packaging materials and bulk/intermediate/finished products.Sample packaging materials and products at various stages.Develop and/or review procedures related to quality activities.Approve/review manufacturing record books.Control and archive batch documentation.Initiate, investigate, and participate in quality events such as out-of-specification results, out-of-trends, deviations, change controls, CAPA actions, complaints, rejections, returns, and recalls.Prepare documentation for registration processes.Participate in internal and external audits, including customer and regulatory inspections, especially visual inspection areas.Assist in establishing corrective and preventive action plans for the quality assurance department.Join us and be part of building the bridge between life-changing therapies and patients.Let’s talk future.Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity / Affirmative Action Employer. We do not unlawfully discriminate based on race, color, religion, age, sex, creed, national origin, ancestry, citizenship, marital or civil union status, familial status, sexual orientation, gender identity or expression, genetics, disability, military status, or veteran status.
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