Pharma documentation jobs in Dahej

 ..., Admin and Quality team. ~ Compliance to process safety and environmental protection code as per BASF Practice. ~ Ensure the documentation of Responsible care requirement on continual basis. ~ Act as EHS representative in the shifts. ~ As a Part of ERT(Emergency Response... 

 ...ensure timely completion with required quality standards. Assist in optimizing production efficiency and minimizing downtime. 2. Documentation & Compliance Maintain and update Batch Production Records (BPR) and other GMP documents accurately. Ensure proper... 

 ...and stock audits; resolve discrepancies. Maintain accurate documentation and ERP/WMS records. 3. Team & Coordination Supervise warehouse...  ...warehouse/store management experience (preferably in Food Pharma or regulated industry). Knowledge of GMP & food safety standards... 

 ...regulations. Coordinate with government authorities for inspections and audits. Maintain statutory records returns and environmental documentation. Support environmental audits and sustainability initiatives. 3. Maintenance & Troubleshooting Plan preventive and... 

 ...viable customer solutions. Partner with product stewardship and HSE to assess and manage product risks, safety data, and compliance documentation.       Requirements (education, experience, competencies and specific job requirements): ~ Ph.D. in Chemistry or... 

 ...system products for key parameters on monthly basis Unsafe Act / Unsafe Condition/ Stop card/ Quality near miss to be reported with documented evidence on monthly basis in coordination with quality control officer Monitor and review MSDS management for Turbhe plant ensure... 

 ...calibration data for all laboratory equipment as per laboratory calibration plan and all ISO related activities. Follow ISO quality and documentation requirements. Adhere to EHS guidelines and identify potential safety risks in laboratory operations. Maintain good... 

Roles and Responsibilities: * Overall responsibility for performance safety quality cost and compliance of assigned manufacturing plant(s). * Convert production plans into daily/shift targets and ensure adherence to output quality and material norms. * Monitor deviations...

About Cliet: Leading speciality chemicals agrochemicals agrochemicals intermediates and pharmaceutical intermediates manufacturing company. Job Title: Purchase Deputy Manager – Chemical Plant Reports To: Purchase Manager / Plant Head Job Summary: Manage direct...

 ...temperature of furnace and other parameters and to look after day-to-day Maintenance activity and problem solving. Maintain necessary documents and records and reports related to furnace as per ISO and GMP Requirements. # Co-ordinate with Other Departments for the... 

 ...validation verification troubleshooting and specification revisions as per pharmacopeial updates. Review validation protocols APQR QMS documents and analytical reports before submission to QA. Coordinate internal customer and regulatory audits; support market complaint... 

 ...diverse portfolio of Active Pharmaceutical Ingredients (APIs). Roles And Responsibilities: Prepare review and maintain QA documents including Validation Master Plan Site Master File Drug Master File Annual Product Quality Review SOPs COAs and audit reports.... 

VIBRATION ANALYST Start Date Starts  Immediately CTC (ANNUAL) Competitive salary Competitive salary Experience ...

About the Company We are a leading API manufacturing organization in India, ranked among the top pharmaceutical companies globally, with multiple USFDA-approved manufacturing facilities. The company has a strong presence in regulated markets including the United States, Europe...

About Client: Client is among the Top 10 Pharmaceutical API Manufacturers in India cater to both domestic and international markets with a diverse portfolio of Active Pharmaceutical Ingredients (APIs). Job Title: HR Manager – Plant HR Reporting To: HR Head Job Summary...