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47 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

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

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

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

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

  • We are currently sourcing profiles for the following Opening: Designation: DGM-QC Job Location: Aurangabad Qualification: M.Sc/M.Pharma Expierence: 10-15yrs 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 ...

  • Operation of GC & HPLC in Pharma & chemical company. Operation of spectrometer, Visco meter, PH meter.Other related operation experience in Lab equipment. Assess relevant regulatory status of products to ensure legal compliance for customers. Ensure & perform effective communication of regulatory status satisfy customer demand. Assess customer requests & define harmony Good knowledge of analytical chemistry ...

  • 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 ...

  • To assist Asst. QC Manager / QC Manager to carryout day to day microbiological analysis as per requirement. To update SOPs, specification and testing methods related to microbiological activities prepared by Asst. Microbiologist. To co-ordinate with National Chemical Laboratory to procure standard Candidates should be B.Sc. / M.Sc. (with Microbiology) and approved by FDA in Microbiology Section. Candidates ...

  • 1. QA :- API Plant Exp :- 5 to 10 Years Qualification :- B.Sc or M.Sc Place of Posting :- Sotonala, Behror, Rajasthan. No of Open Position :- 10 2. QC :- API Plant Exp :- 5 to 10 Years

  • ANALYTICAL R&D, METHODS, VALIDATIONS, QC KNOWLEDGE, CALIBRATION, FORMULATION DEVELOPMENT, GMP/GLP, SOP/ STP, DOCUMENTATION, TROUBLESHOOTING GC, HPLC. ANALYTICAL R&D IN FORMULATION, KNOWLEDGE OF ICH GUIDELINES, CONDUCT MULTIMEDIA DISSOLUTION, ANALYSIS OF THE DEVELOPMENTAL SAMPLES AND STABILITY SAMPLES AT EACH STAGE OF FORMULATIONS DEVELOPMENT, FOLLW GLP, SOP & STP ...

  • 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 ...

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