68 applicants

Company

Original Job Post

Eclaro · 5 days ago

QA Specialist

New Brunswick, NJ

Full-time

Onsite

Mid, Senior Level

5+ years exp

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Responsibilities

Provides oversight for CMO Batch Production Records.

Reviews executed Batch Records, GMP documents and prepare documentation for product release / disposition.

Assists with Document Control and other QA functions.

Coordinates and assist in timely review of documentation associated with manufacturing at CMO site.

Assists with preparation for FDA and other regulatory agency audits and inspections.

Provides daily summaries and follows the completion of CAPAs from audit findings.

Gives guidance to CMO as needed and ensure CMO is compliant with Client Quality standards.

Ensures that all audit items are resolved. Supports site for Inspection.

Reviews any Quality Events, CAPAs from internal and external audits to ensure that actions necessary to provide adequate confidence that the cGMP requirements are completed on time.

Escalates critical quality problems to Senior Management in a timely manner.

Qualification

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QA Site OperationsQA SystemsValidations SupportPharmaceutical Industry KnowledgeBiotechnology Industry KnowledgeEnglish Language FluencyQuality Oversight CoordinationGMP ComplianceBatch Records ReviewLog ReviewManagement CommunicationManufacturing CollaborationError DetectionProblem-SolvingEffective CommunicationDetail-OrientedCGMP QualityQuality SystemsBiopharma Production Processes21CFR 210-211ICH guidelinesFDA Guidance for Industry for Investigating OOS ResultsDeviationsCAPAsValidationStability StudiesQC laboratory operationsManufacturing operationsAuditing

Required

BS in Life Sciences or equivalent with 5+ years related experience within a pharmaceutical or Biotechnology Company.

Hands-on QA Site or ExM Operations / QA Systems experience including supporting Validations within pharmaceutical or Biotechnology Company.

Must be fluent in English language.

Ability to Coordinate Quality oversight and working with other site groups.

Ability to review Quality documents and ensuring compliance to GMP. Documents to include batch records, logs, and others.

Ability to be an effective communicator to Management, and line staff.

Ability to work with other manufacturing teams to implement business objectives.

Must be very detail oriented and be able to quickly detect errors within documentation.

Preferred

Additional experience in an area allied with cGMP Quality, Quality Systems, Biopharma Production Processes, 21CFR 210-211, ICH guidelines, FDA Guidance for Industry for Investigating OOS Results, Deviations, CAPAs, Validation, Stability Studies, QC laboratory operations and manufacturing operations, auditing is preferred.