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97 jobs found for Pharma Plant Fitter

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  • Monitor the required data of consumable like water, electricity, fuels & gases, etc. Preventive maintenance, mechanical work related to all equipment's, feedback & record in break down register. Min 2 years exp in chemical plant as a fitter Immediate joining. ITI (MMCP) / (Fitter ...

  • Qualification: M.Pharma/B.Pharma Experience: 15 Yrs to 20years CTC: As per Industry Std. Gender: Male Reporting to: Managing Dicretor

  • Should have vast experience & expert in Pharma Formulation Manufacturing, Administration, Engineering , Utilities ,cGMP -RA Guidelines ,Communication ,Business development & handling of plant Independently as a profit center. Industry Medical / Healthcare / Hospitals functional Area

  • For a leading pharmaceutical company in Vadodara, Gujarat. we have an opening for Pilot Plant Department. Having experience of 2 - 10 Years for various posts: - Officer - Sr. Officer - Executive - Sr. Executive Asst Manager

  • For a leading pharmaceutical company in Vadodara, Gujarat. we have an opening for Pilot Plant Department. Having experience of 2 - 10 Years for various posts: - Officer - Sr. Officer - Executive - Sr. Executive Asst Manager

  • To ensure timely deliveries of products as per marketing, focus on Quality, Cost & Productivity. Review PPMC monthly production plan. Ensure quality compliance in line with international regulatory requirements. ensure corrective actions Industry Pharma / Biotech / Clinical Research

  • -Should have exposure in handling softgel product. -Experience of working in regulated plant

  • 1. Preparation & Up gradation of Standard Operation Procedures formats and designed new documents as per global quality standards. 2. Compilation of data for API Drug Master Files for US and European markets. 3. Preparation of Daily and Monthly GMP reports & annual budget for up gradation as per cGMP & regulatory requirement and planning accordingly. 4. Maintaining cGMP in manufacturing area and training of ...

  • 1. Preparation & Up gradation of Standard Operation Procedures formats and designed new documents as per global quality standards. 2. Compilation of data for API Drug Master Files for US and European markets. 3. Preparation of Daily and Monthly GMP reports & annual budget for up gradation as per cGMP & regulatory requirement and planning accordingly. 4. Maintaining cGMP in manufacturing area and training of ...

  • 1. Preparation & Up gradation of Standard Operation Procedures formats and designed new documents as per global quality standards. 2. Compilation of data for API Drug Master Files for US and European markets. 3. Preparation of Daily and Monthly GMP reports & annual budget for up gradation as per cGMP & regulatory requirement and planning accordingly. 4. Maintaining cGMP in manufacturing area and training of ...

  • 1. Preparation & Up gradation of Standard Operation Procedures formats and designed new documents as per global quality standards. 2. Compilation of data for API Drug Master Files for US and European markets. 3. Preparation of Daily and Monthly GMP reports & annual budget for up gradation as per cGMP & regulatory requirement and planning accordingly. 4. Maintaining cGMP in manufacturing area and training of ...

  • 1. Preparation & Up gradation of Standard Operation Procedures formats and designed new documents as per global quality standards. 2. Compilation of data for API Drug Master Files for US and European markets. 3. Preparation of Daily and Monthly GMP reports & annual budget for up gradation as per cGMP & regulatory requirement and planning accordingly. 4. Maintaining cGMP in manufacturing area and training of ...

  • 1. Preparation & Up gradation of Standard Operation Procedures formats and designed new documents as per global quality standards. 2. Compilation of data for API Drug Master Files for US and European markets. 3. Preparation of Daily and Monthly GMP reports & annual budget for up gradation as per cGMP & regulatory requirement and planning accordingly. 4. Maintaining cGMP in manufacturing area and training of ...

  • Responsible for manufacturing & support functions of the USFDA/Regulated markets oral solids plant in Pune having around 1000 employees. The Production head, EHS head, HR and all support functions of the plant will report into him Person with around 15 years of experience who is GM or VP level in any Pharma plant handling oral solids, should have faced USFDA audits ...

  • Responsible for manufacturing & support functions of the USFDA/Regulated markets oral solids plant in Pune having around 1000 employees. The Production head, EHS head, HR and all support functions of the plant will report into him Person with around 15 years of experience who is GM or VP level in any Pharma plant handling oral solids, should have faced USFDA audits ...

  • Responsible for manufacturing & support functions of the USFDA/Regulated markets oral solids plant in Pune having around 1000 employees. The Production head, EHS head, HR and all support functions of the plant will report into him Person with around 15 years of experience who is GM or VP level in any Pharma plant handling oral solids, should have faced USFDA audits ...

  • Should have direct exposure of handling pharma R/M & P/M products Experience of working in regulated plant will be preferred Candiadate preferred from PHARMA industry.Purchase dept ...

  • Diploma Mechanical / ITI Fitter with experience in operation & maintenance of the purified water plant at any reputed pharmaceutical - API/bulk drugs/Formulations co ...

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