61 Job openings found

Position:          Executive/Asst. Manager - QA. Location:         Daman Experience:     2 - 5 Years Industries:      Pharma Responsibilities: Handling of out of Specification (OOS), Out of Trend (OOT), Out of Calibration (OOC) and Lab Event investigations. Sporadic Review of stability. PM, RM, FP, SF, SFP, in-process and process validation reports. Review of SOPs, STPs ...

Position:          QC Officer Location:         Sarigam near by Vapi Experience:     2 - 5 Years Industries:      Pharma Responsibilities: Microbiological Testing: Perform routine testing on raw materials, in-process materials, and finished products. Sterility & Endotoxin Testing: Conduct sterility and endotoxin testing to ensure product safety. Documentation: Accurately document test results, ...

We are looking a skilled and experienced QC / Lab Incharge for our distillery plant to oversee quality control operations and laboratory functions. The ideal candidate will be responsible for ensuring compliance with quality standards, monitoring production processes, and leading the laboratory team to maintain product integrity and safety. Education: B.Sc. ...

Key Responsibilities:- Monitor Production Processes: Oversee and document the production process toensure adherence to safety and quality standards.- Conduct Inspections and Tests: Perform routine inspections and quality tests on rawmaterials and finished products to identify potential food safety issues and deviationsfrom established standards.- Compliance and Documentation: Ensure compliance with local, ...

    Technical skills &  Competencies / Language Technical competence.  Leadership skills.  Analytical ability.  Planning ability.  Communication skills.  Problem solving.  Team building.  KEY ACCOUNTABILITIES  Analysis and approval  Sampling, analysis and ascertaining quality of raw materials, packaging material, intermediates, In-process samples and API for Chemistry Ankleshwar.  Testing of the method validation samples and process validation samples and cleaning validation.  Perform analysis and documentation of API finished ...

Position:          Trainee Microbiologist Location:          Daman Experience:       Fresher Industries:       Pharma  Responsibilities: GOOD KNOWLEDGE OF MICRO  WATER VALIDATON  AREA MONITORING  ROUTINE ANALYSIS OF SAMPLE. VALIDATION OF MICRO AND PREPARATION OF PROTOCOL   Required Skills Must be excellent in written and spoken English; net savvy and adept at computer skills. Logical thinking. Organizing. Good in communication.   Required Qualification: - B.Sc/M.Sc ...

  Job Overview - Routine Microbial Analysis of Raw Material & Finish Good Samples Routine Calibration Environment Monitoring Media preparation Product Stability Documentation Report Preparation   Responsibilities and Duties- - Prepare monthly, quarterly and annual sampling plan, Validation plan and/or qualification plan - Prepare and implement stability plan for all products. - Daily Reporting and release of Raw materials and finished goods - Co-ordination ...

Internal Job Description Education / Experience  M.Sc. Analytical/Organic Chemistry/Inorganic Chemistry  Min. 5 years’ Experience in a Quality Control/Analysis laboratory in a cGMP/ISO environment, with exposure to method development and validation activities  Technical skills &  Competencies / Language Technical competence.  Leadership skills.  Analytical ability.  Planning ability.  Communication skills.  Problem solving.  Team building.  KEY ACCOUNTABILITIES  Analysis and approval  Sampling, analysis and ascertaining quality of raw materials, packaging ...

Position:          Sr. Executive/ Asst. Manager - QA Location:         Vapi Experience:      8 - 12 years Industries:       Pharma API   Responsibilities: QMS handling like, change control, deviation, market compliant, returned product, SMF, Quality manual, VMP, and  New BMR , BPR preparations or revisions. Audit work ,preparation for compliance ...

Environment/Pathogen Monitoring Program, Sampling & Testing of Pkg. material, raw material, finished goods, EMP sample preparation and sterilization microbiological media, Tracking, Weekly Biological indicator test for Autoclave, growth promotion test Should be aware of ISO & USP guideline for Microbiology. Good knowledge of GMP practices Responsible for Decontamination of Bio-hazard waste generated from ...