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  • Pharma Department:-Formulation Job Profile: Candidates should have exposure of FP/in-process/process validation/analytical data review/stability. Experience of instruments like HPLC, UV-Spectrophotometer, Particle Size analyser, KF-Autotitrator (Metrohm), Dissolution test apparatus, ICPMS ...

  • 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

  • Interview held in Vapi&INDORE On 18th December. , 24TH DEC AT AHMEDABAD Job Profile: 1. Handling GC, UV. 2. Having knowledge of Formulation 3. Having Experience in tablet,Capsule. Waiting your revert. If you have any query, request you to kindly reach on below contact details: Department: QC Experience ...

  • 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 ...

  • Position - QC Team Leader - Implementation Location - Bonthapally, Andhra Pradesh, India Purpose of the job - To provide analytical support to production for routine QC releases. Responsible for the best and cost effective utilization of the available resources for timely deliveries. GMP compliance

  • 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 ...

  • 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 ...

  • Developing SOP & quality manualBenefits?Best in the IndustryClient Introduction?One of the well known brands and having spread across India ...

  • 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 ...

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