Senior Specialist QA – Quality Assurance
BioPharma Consulting JAD Group · Juncos
Job description
About the role
The Senior Specialist, Quality Assurance acts as a technical expert supporting quality systems, validation activities, and regulatory compliance in a regulated manufacturing environment. The role reviews and approves product documentation, validation protocols, environmental reports, and quality records while leading investigations and cross‑functional initiatives.
Key responsibilities
- Review and approve product manufacturing procedures (MPs) and process validation protocols.
- Approve environmental characterization reports and planned incident documentation.
- Release sanitary utility systems in accordance with quality requirements.
- Represent Quality on incident triage and New Product Introduction (NPI) teams.
- Serve as designee for the QA Manager on the local Change Control Review Board (CCRB).
- Collaborate with Manufacturing, Facilities, Utilities, Validation, and Process Development teams.
- Lead investigations and ensure timely closure of quality events.
- Own and maintain site quality program procedures and perform advanced data trending and compliance assessments.
Required profile
- Doctorate + 2 years of directly related experience OR Master’s + 4 years OR Bachelor’s + 6 years OR Associate’s + 10 years OR High School/GED + 12 years.
- Strong knowledge of manufacturing, distribution, QA, QAL, validation, and process development.
Required skills
- KNEAT, CDOCS, SCADA, TrackWise, Maximo.
- Good Documentation Practices (GDP) and Data Integrity compliance.
- Computer System Validation (CSV) and equipment validation.
- Facilities & Utilities commissioning and qualification.
- Risk assessments and risk management.
- SOP development, revision, and document review/approval.
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Published 1 week ago
Expires 1 month from now
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BioPharma Consulting JAD Group
Juncos
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