Senior Executive-Quality Assurance-Oncology(Formulation Sterile Inj)
24 hours ago
Roles and Responsibilities
- Conduct BPR review, BMR review, Change Control, Cleaning Validation, Deviation investigation, IPQA activities, Process Validation, QMS implementation, and Quality Assurance for Formulation Sterile Injectables.
- Ensure compliance with regulatory requirements and company policies.
- Collaborate with cross-functional teams to resolve quality issues and improve processes.
- Develop and maintain documentation related to quality control procedures.
- Participate in audits and inspections conducted by regulatory authorities.
Desired Candidate Profile
- Strong understanding of Good Manufacturing Practices (GMP), Current Good Laboratory Practice (cGMP), and Quality Management System (QMS).
- Bachelor's degree in Pharmacy (B.Pharma) or Science (B.Sc).
- 2-7 years of experience in pharmaceutical industry with expertise in formulation sterile injectable products.
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