Average salary: Rs439,929 /yearly
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- ...Plant Details : USFDA Formulation (OSD & Sterile) Manufacturing Plant Job Location : Daman Position : Senior Manager - Engineering (Utilities) Role : Section Head Positing Reports to : HOD - Engineering @ Daman Key Responsibility Areas: A) Budgetary Control...SuggestedFull time
- Data and Documentation Review: Perform rigorous independent review of analytical raw data calculations instrument audit trails and final reports (including OOS and deviation investigations) to ensure compliance with quality standards (ALCOA). Compliance Oversight: Review...SuggestedFull time
- ...Identify and resolve manufacturing deviations aseptic failures and process inefficiencies to ensure continuous improvement. Coordination & Training: Work closely with QA QC and Engineering teams and train staff on sterile handling gowning and aseptic techniques ....SuggestedFull time
- Environmental Monitoring: Conduct regular environmental monitoring of critical areas including clean rooms production areas and laboratories to ensure compliance with microbial limits. Microbial Testing: Perform microbiological testing on air surface water and personnel...SuggestedFull time
- The Senior Officer QC (Validation) will be responsible for testing and analysis of sample to ensure compliance . Perform validation activities for QC instruments equipment and analytical methods as per regulatory guidelines (USFDA EU ICH). Execute calibration qualification...SuggestedFull time
- Job Purpose This position is open with Bajaj finance limited The Branch manager is a managerial responsibility for providing full leadership and direction to the team of employees in growing business and client base of consumer gold loan. The overall objective of this...SuggestedFull time
- ...levels strictly comply with ALCOA principles and global regulatory standards. QMS & Audit Compliance: Lead investigations for engineering deviations implement CAPAs draft Change Controls and represent the automation/maintenance department during regulatory audits (...SuggestedFull time
- Raw Material Testing: Perform physicochemical and instrumental analysis (HPLC GC UV FTIR Titrations) of raw materials and excipients. Compliance & Documentation: Maintain test records COAs and laboratory documentation as per GMP GLP and data integrity guidelines...SuggestedFull time
- Plant Details : USFDA Formulation Manufacturing Plant based at Daman near Vapi (Gujarat). Position : Manager - Production QMS (Sterile) Position Reports to : Senior Manager -Production(Sterile) Desired Qualification : / Job Description: 1. Change control/ Deviations...SuggestedFull time
