Founded in 1989, Sudeep Pharma Private Limited is a pioneering force in the pharmaceutical industry, excelling in excipient and mineral actives manufacturing. Renowned for innovation, the company has expanded into specialty pharmaceutical ingredients and diversified into Food and Nutrition Segments, integrating advanced technologies to stay ahead of industry trends.
Post : Assistant Manager - Regulatory Affairs
Job Description
• To attend to all technical queries from the customers.
• To update all specification and to verify with the production and QC team.
• To update all customer specification and to verify with the production and QC team.
• To make record of the special requirements of the customer
• To arrange and analyze the raw materials and finished product testing results to help management take decisions.
• To analyze complaints product wise and unit wise for management review.
• To manage and review the sample requests received form customers.
• To co-ordinate with the QC team of the customers where harmonization of test methods is required.
• To co-ordinate with the Production team of the customers where modification of our product quality is required.
• To attend to customer complaints by email conversation and review of the CAPA effectiveness with concern department.
• To co-ordinate R&D and QC in development of new products.
• To help co-ordinate with the customer with their vendor qualification procedure.
• Additional work as per requirement. In absence of her, her colleague is responsible to complete her work.
Additional Information
Experience : Minimum 6 years
Qualification : B.Pharm, M.Pharm, M.Sc.
Location : Nandesari, Vadodara
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Regulatory Affairs
End Date : 30th March 2024
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