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57 jobs found for Qc Pharma

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  • Designation: Sr.GM-QC (Formulation) Job Location: Gujarat Qualification: M.Sc/M.Pharma Expierence: 15 yrs & Above Salary: As per industry std. Description: -Candidate having more than 15 yrs Expirence into Quality Control (Formulation). - Candidate should have work expirence in USFDA Approved

  • Designation: Sr.GM-QC (Formulation) Job Location: Gujarat Qualification: M.Sc/M.Pharma Expierence: 15 yrs & Above Salary: As per industry std. Description: -Candidate having more than 15 yrs Expirence into Quality Control (Formulation). - Candidate should have work expirence in USFDA Approved

  • Job Location: Aurangabad Qualification: M.Sc/M.Pharma Expierence: 10-15yrs Salary: As per industry std ...

  • We have urgent opening for the position of QC Micro at Vapilocation leading pharma company. Designation: QC Micro Experience: 3 to 10 Year Location: Vapi

  • Designation: DGM-QC Job Location: Daman Qualification: M.Sc/M.Pharma Expierence: 10-15 yrs Salary: As per industry std ...

  • About Our Client Co. Our Client Co is leading & fastest Growing Pharma with Corporate office & RD Center in Mumbai & 4 Manufacturing Plants located across India. Position: Officer/Executive-Quality Control Location: Dahej, Bharuch Exp: 1 to 7 Yrs Qualification & Experience: MSC / M. Pharma, B ...

  • 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 ...

  • of the documental records to be prepared by Q.C. Department for authorization and detailed specification for – a. All materials ii) Regents iii) Solvents & iv) Water. 18. Complain investigation recording format and its proper implementation. 19. Specification records to be prepared for: i. Raw Materials. ii. Job Description ***Urgent Opening for "Lab Chemist" (QC/ Production) for leading Pharmaceutical company in ...

  • process with the business needs of our clients. We believe in providing a solution for all the HR related activities. About Our Client Co. Our Client Co is leading Pharma with Corporate office & RD Center in Mumbai & 4 Manufacturing Plants located across India. Here below Mentioned is Detailed JD Note ...

  • 1. QA :- API Plant Exp :- 5 to 10 Years Qualification :- B.Sc or M.Sc

  • Openings for 1) Production Incharge 2) QC Incharge cum Microbiologist for our medical device manufacturing unit located in Malur. 1) for Production Incharge : Minimum BSC qualification or B Pharma, M Pharma, D-Pharma will also do. 2) For QC incharge : BSC with Microbiology or Biotechnology Graduate. Experience : Minimum 1 year at least. Should be able to shift to Malur or should be able to travel to Malur daily ...

  • Walk in at VAPI for (QC-HPLC-GC & AMV) for Gujrat & Indore Location 1. HPLC Officer -7 2. Analytical Officer-2 3. Microbiologist Officer -2 Note -They must have experience of minimum -3 to 4 years of pharma industry in formulation division ...

  • Walk in at VAPI for (QC-HPLC-GC & AMV) for Gujrat & Indore Location 1. HPLC Officer -7 2. Analytical Officer-2 3. Microbiologist Officer -2 Note -They must have experience of minimum -3 to 4 years of pharma industry in formulation division ...

  • Operator - 20 position - Injection Filling QA/QC - 20 position (BSC/MSC/Bpharma/M pharma 3 to 8 year Exp)Budget 3 to 7 lac Production - Tablet as well as Injection 3 to 10 year

  • Walk - in Interview at PUNE 26 FEB for Formulation/Sterile -QA/QC/Prod. Operator - 20 position - Injection Filling QA/QC - 20 position (BSC/MSC/Bpharma/M pharma 3 to 8 year Exp)Budget 3 to 7 lac Production - Tablet as well as Injection 3 to 10 year

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