Roles and Responsibilities :

• Initiation/Review of change control, impact assessment and management of change control records.
• Preparation of Annual Product Quality Review & MRM record.
• Review of Vendor questionnaire and related documents.
• Handling of deviation, market complaints, out of specification and CAPA.
• Review of Investigation of Deviation, OOS & Other Non-Conformities.
• Review Of Validation, Qualification CSV Document.
• Release of Intermediate in absence of Manager-QA
• Conduct GMP/ Regulatory Training.
• Conduction Internal Audit.
• Review of analysis data of finished product before release.
• Preparation and Review of SOPs, BPRs, Specifications and STPs, Protocols, Quality manual, MSDS.
• Review of stability data provided by QC.
• Updating of Master Formats, Master document Index and Master Format List.

One of the largest manufacturers of Vitamin D3 and a key global player. Headquartered in Thane, India. The company caters to clientele across the globe, with a worldwide distribution network. Its state-of-the-art R&D centre is based at Thane, and world class manufacturing facilities are located in Kullu, Himachal Pradesh and Dahej, Gujarat. Apart from Vitamin D3, It also offers niche APIs, integrated biotechnology platforms such as enzymes for antibiotic synthesis as well as environmental solutions for waste water management and treatment.