11 Job openings found

Media Section Supervisor Jobs in Pharma | Pharmaceutical Production & Media Preparation Careers – Orbit Global HR Consultants Job Title: Supervisor – Media SectionJob Location: To be confirmed with the hiring companyDepartment: Pharmaceutical Production / Media PreparationIndustry: Pharmaceutical / Biopharmaceutical ManufacturingEmployment Type: Full-Time, Permanent (subject to confirmation)Hiring Company: Confidential Pharmaceutical CompanyRecruitment ...

Cell Culture Production Jobs in Hyderabad | Pharma Manufacturing Careers Job Title: Cell Culture Production Manager / ExecutiveJob Location: Hyderabad, TelanganaDepartment: Production – Cell CultureIndustry: Pharmaceutical / Biopharmaceutical ManufacturingEmployment Type: Full-TimeHiring Company: Confidential Pharmaceutical CompanyRecruitment Partner: Orbit Global HR Consultants LLPExperience Required: To be confirmedSalary: As per experience and industry standardsJob ...

Position:       Sr. Officer/Executive/Sr.Executive - Microbiology Location:       Ahmedabad Experience:    4 - 6 Years Industries:     Pharma   Responsibilities Temperature, RH and Differential pressure monitoring of Microbiology Lab areas and refrigerator. Microbial limit test, Pathogen and Bio-burden test of Raw material, Finished product as per current version of Specification and STP Sampling of water Chemical and Microbial ...

Position: Micro Officer Location: VAPI- GUJARAT Experience: 1 to 3 Years Qualification: B. Sc/ M. Sc- Micro/ Biotechnology   Job Description: Water Sampling & Analysis: - Collection and microbiological testing of purified water, WFI, and utility systems - Trending and reporting of water quality parameters Environmental Monitoring: - - - Routine monitoring of clean rooms, ...

Actual Vs. Documentation Microbial limit test finish product (A) Second day, (B) Forth day. Microbial limit test water sample(A) Second day (B) Forth day. Microbial limit test swab test(A) Second day (B) Forth day. Grovåh promotion test (A) Mannitol salt agar, (B) Cetrimide agar, (C) MacConkey's Broth, (D) Rappaport Vassiliadis Salmonella Enrichment Broth, (E) Nutrient ...

Actual Vs. Documentation Microbial limit test finish product (A) Second day, (B) Forth day. Microbial limit test water sample(A) Second day (B) Forth day. Microbial limit test swab test(A) Second day (B) Forth day. Grovåh promotion test (A) Mannitol salt agar, (B) Cetrimide agar, (C) MacConkey's Broth, (D) Rappaport Vassiliadis Salmonella Enrichment Broth, (E) Nutrient ...

Actual Vs. Documentation Microbial limit test finish product (A) Second day, (B) Forth day. Microbial limit test water sample(A) Second day (B) Forth day. Microbial limit test swab test(A) Second day (B) Forth day. Grovåh promotion test (A) Mannitol salt agar, (B) Cetrimide agar, (C) MacConkey's Broth, (D) Rappaport Vassiliadis Salmonella Enrichment Broth, (E) Nutrient ...

Assist in ensuring product quality and compliance with regulatory standards, including MDR and QMS requirements. Support the preparation and maintenance of quality manuals, formats, and SOPs under guidance. Conduct routine document reviews, including COAs, calibration reports, and sterilization checklists. Participate in internal audits and assist with audit documentation and follow-ups. Maintain and update records ...

  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 ...

Quality Assurance Specialist Responsibilities: Ensure product quality and conformity to regulatory standards, including Medical Device Regulation (MDR) and Quality Management System (QMS). Conduct internal quality audits and participate in management review meetings. Handle investigations of complaints and implement corrective and preventive actions. Maintain and update quality manuals, formats, and standard operating procedures (SOPs) in ...