Regulatory Affairs Job Vacancies in Palghar

  • 6 - 12 yrs
  • 12.0 Lac/Yr
  • Palghar Thane
Dossier CDSCO State FDA Of Drugs and Cosmetics Act & Rules
Urgent OpeningRegulatory Affairs Manager (Veterinary Pharmaceuticals)Veterinary Pharmaceutical Manufacturing CompanyPalghar, MaharashtraQualification B.Pharm / M.Pharm / M.V.Sc. / M.Sc. or an equivalent qualification. Additional certification in Regulatory Affairs will be an added advantage. Experience 8-12 years of experience in Regulatory Affairs within the veterinary or pharmaceutical industry. Experience in handling product registrations and regulatory approvals. Regulatory Affairs Manager to oversee all regulatory activities for veterinary pharmaceutical products. The candidate will be responsible for product registrations, dossier preparation, regulatory submissions, license management, and ensuring compliance with all applicable veterinary pharmaceutical regulations.Key Responsibilities Manage regulatory affairs activities for veterinary pharmaceutical products. Prepare, review, and submit product registration dossiers to regulatory authorities. Coordinate with the CDSCO, State FDA, and other regulatory authorities for approvals and licensing. Ensure compliance with the Drugs and Cosmetics Act & Rules, Schedule M, GMP, and other applicable regulations. Prepare and maintain regulatory documentation, technical files, and product dossiers. Handle applications for manufacturing licenses, product permissions, and renewals. Coordinate with QA, QC, Production, R&D, and Marketing departments for regulatory compliance. Review product labels, package inserts, and artwork to ensure regulatory compliance. Respond to regulatory queries and deficiency letters from authorities. Monitor changes in regulatory guidelines and implement necessary updates. Support internal, customer, and regulatory audits. Maintain regulatory records and ensure timely submission of required documents. Required Skills Strong knowledge of Veterinary Pharmaceutical Regulations. Experience in CDSCO, State FDA, and product registration processes. Knowledge of Drugs and Cosmetics Act & Rules, Schedule M, and GMP. Ability to coordinate effectively with cross-functional teams and regulatory authorities.
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  • 10 - 14 yrs
  • 15.0 Lac/Yr
  • Palghar Thane
Hard Working Knowledge Of Factory Quality Assurance Regulatory Affairs Production
Urgent OpeningFactory Manager (Veterinary Pharma)Veterinary Pharmaceutical Manufacturing Company. Palghar East, Maharashtra Qualification B.Pharm / M.Pharm / B.Sc. / M.Sc. / B.E. / B.Tech. or an equivalent qualification. Additional qualification in Operations or Industrial Management is an added advantage. Experience 10-15 years of experience in the pharmaceutical or veterinary pharmaceutical industry. Minimum 5 years of experience as a Factory Manager or Plant Manager. The Factory Manager will oversee the overall operations of the veterinary pharmaceutical manufacturing facility in the Company. The candidate should have strong knowledge of Production, Quality Assurance (QA), Quality Control (QC), Warehouse, Engineering, Maintenance, Regulatory Compliance, and Dispatch to ensure smooth plant operations and compliance with GMP and regulatory standards. Key Responsibilities Manage the overall operations of the manufacturing plant. Ensure production targets are achieved as per the production plan. Supervise and coordinate Production, QA, QC, Warehouse, Engineering, Maintenance, and Dispatch departments. Ensure compliance with GMP, GLP, SOPs, Schedule M, and other regulatory requirements. Required Skills Strong knowledge of Production, QA, QC, Warehouse, Engineering, Maintenance, and Regulatory Affairs. Good understanding of GMP, GLP, GDP, Schedule M, and Quality Management Systems (QMS). Experience in handling regulatory inspections and audits. Excellent leadership, decision-making, and people management skills. Strong planning, problem-solving, and communication abilities. Proficiency in MS Office and ERP systems.
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Regulatory Affairs Regulatory Officer Manager Regulatory Affairs Walk in
Roles and Responsibilities :Regulatory/ DMFAsking for necessary technical inputs from various departments in the Factories and doing its assessment.To give the necessary technical inputs required by the respective government departments (FDA, CDSCO ) under the guidance of the Head RegulatoryCompilation, review and submission of DMF (Drug master file) to Regulatory & ROW markets as per the given guidelines.To keep DMF files active as per the agency requirements.Revision/Renewal of CEP.Compilation & submission of Applicants part DMF (Drug master file) & QOS for customers.Compilation & Submission of RP DMF for authorities.Submissions of DMF Annual report to USFDASubmissions of DMF amendments to USFDAReply to the queries raised by respective authoritiesCustomer ServicingResponsible to address different questions and queries (technical) in the given time frame for customersTo get the necessary information from QA, QC for compilation and onward submission to regulatory authorities and customers as response to their queriesTo evaluate the technical agreements /CDA to be signed with the customers as on basis.Review of vendor questionnaire within the required timeframe along with supporting documents to customers and maintaining the record for the same.Preparation of the certificate of suitability for various customersPreparation/review of different kinds of declarations as per customer requirementsReview of change control, customer notification/intimationKeeping the track of customer notification/Intimation and response to the various queries raised by various customers & Log Maintenance Preparation of LOAs
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