Job Description
Min experience of 6-8 years in Quality assurance and regulatory. Graduate or Post Graduate.
Requirements
• Graduate and/or Post Graduate (Pharmacy, Biochemistry, Biotechnology, Chemistry.)
• Knowledge of techniques involving quality assurance of pharmaceuticals antibodies/ Proteins
• On-job knowledge of in vitro MDD / IVD documentation
• Min experience of 6-8 years in Quality assurance and regulatory with preferably IVD/medical devices / injectable in Executive / Managerial position.
• Innovative thinking for solutions of problems arising out of established Quality Management System, Leader
• Good written and spoken English
• Computer proficiency (MS Excel, PPT, Word)
Duties and Responsibilities
• Monitor Implemented Quality Control Systems
• Provide training wherever required
• To conduct Internal audits at regular intervals
• Coordinate Batch failure and OOS Investigations ensuring appropriate Corrective and Preventive actions (CAPA).
• Qualification and Validations (Revalidation) of facility, equipment and processes
• Participate in the Vendor development and audits for raw materials and packing materials
• Support Quality Head in QMS and its effective implementation.
• Support in maintain effectiveness of established strategic vision for the Quality Assurance
💡 Quick Summary
Seeking a career-building opportunity? The Asst| Manager QA and Regulatory position is now open for candidates interested in the Health Jobs sector. This role in Surat offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Health Jobs is a plus.
