Vice President of Quality

20 years

0 Lacs

Posted:2 months ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Job Title: Head (VP) – Quality (Formulations) Location: Bangalore, India Experience Required: Minimum 20 years Function: Corporate QA Industry: Pharmaceutical Formulations Reporting To: Site Head / Corporate Quality Head Job Summary: We are seeking a highly experienced and dynamic Head of Quality to lead the Quality Assurance (QA), Quality Control (QC), and Microbiology functions across two state-of-the-art formulation manufacturing plants based in Bangalore. The ideal candidate must have strong expertise in regulatory audits, QMS, and laboratory operations, with a proven track record of successfully leading international regulatory audits (such as USFDA, UKMHRA, and EU QP audits). The incumbent must have at least 5 years of recent experience handling both QA and QC functions and should possess excellent leadership and compliance management capabilities. Key Responsibilities: Lead and manage the Quality Assurance , Quality Control , and Microbiology functions for both formulation plants. Ensure full compliance with global regulatory requirements including USFDA, UKMHRA, EU, and other international authorities. Oversee the development, implementation, and continuous improvement of Quality Management Systems (QMS) . Lead the preparation and handling of regulatory inspections and customer audits; ensure timely closure of audit observations (CAPA). Ensure effective documentation, data integrity practices, and adherence to cGMP guidelines across all quality functions. Provide strategic guidance to QA and QC teams to ensure the release of raw materials, in-process materials, and finished products as per specifications. Review and approve quality-related documentation such as SOPs, protocols, specifications, and validation reports. Drive laboratory excellence in QC and Microbiology with a strong focus on analytical accuracy and regulatory compliance. Collaborate closely with cross-functional teams including Manufacturing, Regulatory Affairs, and R&D to ensure alignment with business and compliance goals. Mentor, develop, and lead a team of quality professionals across both sites. Candidate Profile: Educational Qualification: M. Pharm / M.Sc. / B. Pharm or equivalent (higher qualifications preferred). Experience: Minimum 20 years of experience in Quality functions in pharmaceutical formulations. At least 5 years of recent experience leading both QA and QC functions . Strong track record in handling international regulatory audits such as USFDA, UKMHRA, EU QP , etc. Deep understanding of QMS , ICH guidelines , cGMP , and data integrity principles. Experience in managing multiple manufacturing sites will be an added advantage. Strong leadership, analytical, and communication skills with the ability to work cross-functionally. Compensation: Competitive and commensurate with experience. Location Flexibility: Candidate must be willing to be based full-time in Bangalore . Show more Show less

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