Site Quality Head OSD

As a Site Quality Head at our reputed pharmaceutical manufacturing company in Vapi, Gujarat, you will play a crucial role in leading and overseeing the Quality Assurance and Quality Control functions at our Oral Solid Dosage (OSD) facility. Your responsibilities will include: - Leading and managing the complete Quality function (QA and QC) at the site - Ensuring compliance with GMP, regulatory, and customer requirements - Overseeing quality systems such as deviations, CAPAs, change controls, validations, and documentation - Monitoring and guiding all laboratory operations, including chemical, instrumentation, and microbiological testing - Preparing for and leading regulatory and customer audits such as USFDA, MHRA, WHO-GMP, etc. - Driving continuous improvement in quality processes and systems - Collaborating cross-functionally with production, supply chain, engineering, and regulatory teams - Developing and mentoring the site's QA and QC teams to foster a strong quality culture To excel in this role, you should possess the following qualifications and experience: - B.Pharm / M.Pharm / M.Sc or equivalent in life sciences - Minimum 15 years of experience in the pharmaceutical industry with significant exposure to OSD manufacturing - Currently working as a Site Quality Head or in an equivalent leadership role - Proven experience in managing both Quality Assurance and Quality Control functions - In-depth knowledge of GMP regulations, audit readiness, and global regulatory expectations - Strong leadership, communication, and stakeholder management skills - Experience in handling regulatory inspections and third-party audits Join us and be part of a company dedicated to delivering high-quality products through robust systems and a strong quality culture.,