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Site Quality Head (VP Quality)
Bharuch, Gujarat, India · Tam zamanlı
Başvuran ilk kişi siz olun
- Deneyim
- 18–25 yrs
- Maaş
- INR 6,000,000 – INR 9,000,000 / year
- Açılışlar
- 1
- Yayınlandı
- 2 gün önce
- Çalışma modu
- Ofiste
- Eğitim
- Master's degree in Pharmacy, Chemistry or related Life Sciences
- Uygunluk
- Candidates currently employed in senior management roles such as Senior GM, AVP, or VP in pharmaceutical quality functions are eligible to apply.
- Sürdürmek
- Başvuru yapılması gerekmektedir.
Çalışacağınız yer
İş tanımı
About the Role and Company
This leadership position as Site Quality Head (VP Quality) is based at a large-scale oral solid dosage (OSD) formulation manufacturing plant in Dahej, Gujarat. The site produces tablets, capsules, and oral suspensions and holds approvals from US FDA and WHO. The plant employs over 2,000 staff, with a quality team exceeding 500 personnel. The company, Pharma Placements, has a strong global presence with annual sales above 500 crore INR, exports to 52 countries, and is launching a new division focused on cosmeceuticals, dermaceuticals, and anti-aging products.
Primary Responsibilities
- Provide leadership for Quality Assurance and Quality Control at the manufacturing facility.
- Ensure strict adherence to cGMP and global regulatory standards including WHO-GMP, US FDA, MHRA, and EU-GMP.
- Design and execute site-specific quality strategies aligned with corporate quality goals.
- Manage batch release processes, investigations, deviations, OOS/OOT events, CAPA actions, change control, and risk mitigation.
- Maintain audit preparedness for regulatory, client, and internal inspections.
- Drive initiatives to continuously enhance quality metrics and processes.
- Collaborate cross-functionally with Manufacturing, Engineering, Supply Chain, Regulatory Affairs, and Corporate Quality teams.
- Lead regulatory inspection management and oversee responses to findings.
- Develop and guide the quality leadership team to foster compliance culture and operational excellence.
Candidate Profile and Eligibility
- Master's degree in Pharmacy, Chemistry or related Life Sciences fields.
- 18 to 25 years of experience in pharmaceutical quality functions, specifically in OSD manufacturing environments.
- Demonstrated leadership in managing quality for large formulation manufacturing plants, preferably US FDA approved.
- Current seniority as Senior General Manager, AVP, or Vice President in Quality roles is required.
- Strong expertise in global regulatory frameworks and proven skills in handling international regulatory inspections.
- Excellent communication, leadership, and stakeholder management capabilities.