What are the responsibilities and job description for the Manufacturing Quality Engineer – Validation position at Talent Groups?
Seeking a Lead Engineer, Quality Validation to oversee process validation, technology transfers, and compliance in biopharmaceutical manufacturing. This role ensures GMP, FDA, and ICH compliance while managing validation activities with internal teams and CMOs .
Key Responsibilities :
- Oversee process validation, qualification, and technology transfers
- Ensure compliance with GMP, FDA, and ICH guidelines
- Conduct risk management, deviations, and process verification
- Collaborate with CMOs and cross-functional teams
- Provide updates and reports to senior management
Qualifications :
8–12 years of experience in biopharma / pharma validation
Strong knowledge of GMP, process validation, and regulatory standards
Experience with CMOs, process transfers, and analytical validation
Excellent problem-solving, communication, and leadership skills
