Qa validation jobs in Palghar

 ...Job Summary: The Quality Assurance (QA) Manager will be responsible for developing, implementing, and managing quality control systems to ensure that products or services meet established quality standards and regulatory requirements. This role involves leading a team of QA... 

 ...documentation including Quality Risk Assessment (QRA), Cleaning Validation, Market Complaints, Self-Inspection, Quarterly Review Reports, Site...  .../ M.Pharm Experience: Minimum 8–15 years of experience in QA Documentation with Pharma Formulations Strong understanding of... 

 ...(COA) for approved raw materials. Ensure all logbooks, registers, and worksheets are properly filled and signed. Coordinate with QA for material release tagging Compliance & Audit Readiness: Adhere to cGMP, GLP, and Schedule M requirements. Follow data integrity... 

 ...operating procedure. Ensure all instruments are calibrated and validations are carried out in timely manner. Issue Validation Protocol,...  ...Regulatory requirement. Any other assignments allocated by Unit QA from time to time responsibilities Stay informed about current... 

CANDIDATE MUST BE FROM INJECTION MOULDING -MANUFACTURING OF SPOUTS, CAPS and CLOSURER INDUSTRY FOR FOOD AND BEVERAGE Overall monitoring & control on Day-to-Day Departmental activities. Overall Responsible for overall control on all Incoming RM, In-process and Finish Product...

 ...compatibility studies. Design and execute lab-scale, exhibit, and validation batches of tablets and pellets using QbD principles. Optimize...  ..., GLP, and global regulatory expectations. Collaborate with QA and Regulatory Affairs during internal and external audits, as... 

To conduct and document analytical method validation (AMV), method verification, and method transfer activities for raw materials, in-process samples, and finished pharmaceutical products in compliance with ICH Q2(R1) , GMP , and regulatory standards . Key Responsibilities... 

 ...Job Responsibilities Perform analytical method development, method validation and query response for the finished product. Prepare analytical method development reports, CDP and COA (Certificate of Analysis) Perform and review analysis of In-process sample/Finished... 

 ...Verify supplier COAs and related test data. Vendor Audits: Plan, schedule, and conduct on-site and remote audits of vendors (with QA audit team). Prepare audit plans, checklists, and audit reports. Follow up on audit observations and ensure timely CAPA implementation... 

Job Responsibilities Responsible for handling all production activities pertaining to Pellets or Granulation. Responsible to handling all manufacturing activities as per Regulatory requirement. Responsible to handle the team to achieve the set targets & maintain qualitative...

Job Responsibilities Optimum machine availability, workforce & shifts of maintenance department, draw PPM plan & execute it. CGMP instructions to be followed, solve all technical issues, machine maintenance, care of safety & environmental pollution aspects, breakdown ...