Engr 3, Quality

Must Have 21 CFR Part 210/211 BS in scientific/technical field (or equivalent experience) Direct CAPA authoring Investigation writing Pharmaceutical/Drug Manufacturing Technical Review Nice To Have Cleaning ValidationsEquipment Validation, Transfer, and Qualification

ICH Q9 OOS

Investigations Supplier Assurance Role:

GMP professional to support CAPA deliverables as part of a broader quality remediation initiative, bringing strong knowledge of 21 CFR Part 211 requirements and demonstrated expertise in technical writing and document review within a regulated environment. The ideal candidate will be capable of independently driving high-quality, inspection-ready outputs while partnering with cross-functional teams and contributing to a risk-based approach to compliance, with additional value placed on familiarity with ICH Q9 principles — key capabilities include: Develop and execute CAPA records, ensuring alignment with regulatory expectations and internal quality standards Perform thorough technical writing and critical review of investigations, protocols, and reports Apply 21 CFR Part 211 knowledge to ensure GMP compliance across deliverables and identify potential risks or gaps Collaborate with SMEs and functional teams to drive timely closure of CAPAs and maintain project timelines Additional desired skills in risk assessment and risk management to contribute to or author/review risk assessments using a structured, science- and risk-based approach (ICH Q9 experience preferred)