23 Job openings found

Duties & Responsibility :·       Quality Management System Implementation and Modification control.·       Document Control.·       Approval for batch release.·       Review and approval of Qualification Document.·       Review and approval of Calibration and Validation document.·       Planning, execution and compliance of both internal and external audits.·       Preparation of audit compliance report·       Review and approval ofSMF, VMP and Quality manual.·       Review and approval of BMR, ...

A Deputy Manager - Quality in a chains manufacturing company (such as industrial, automotive, or conveyor chains) is responsible for upholding stringent quality standards for raw materials, in-process production, and finished products. The role focuses on preventing defects, implementing QMS (IATF 16949/ISO), and driving continuous improvement (Kaizen/Six Sigma).      Core Responsibilities: Supplier Quality Management ...

Job Responsibilities: Maintain QMS documentation, SOPs, training records & audit readiness Conduct internal audits for clinical, BE & pharmacovigilance operations Support vendor audits, gap assessments, CAPA tracking, compliance reviews Ensure adherence to ICH GCP, regulatory guidelines & quality standards Required Qualification: B.Pharm/M.Pharm/MSc in Life Sciences 1–3 years experience in QA within CRO/BE/Clinical Trial setup Understanding of QMS, risk ...

Position:           Manager Microbiology Location:          Daman Experience:      5 - 10 YEARS Industries:       Pharma Responsibilities: Experience in vaccine and biological (Mabs) manufacturing, Handled greenfield / brownfield – Microbiology lab, qualification and validation of Microbiology lab and instruments, preparation and review of all Microbiology documents such as SOPs, protocols, reports, etc., USFDA and EU ...

Hiring for Grade starches Pharmaceutical Products Manufacturing Industry Position: - QC Manager Education: MSc / BSc Experience: Min 7 years experience in Pharma Company Having good knowledge of QMS documentation like change control, deviation, CAPA, OOS, Qualifications, vendor handling.... etc Location: - Dondaicha – Nandurbar MH If you are interested kindly send your updated CV   For ...

Hiring for Grade starches Pharmaceutical Products Manufacturing Industry Position: - QC officer- Education: MSc / BSc Analytical Experience: 3 -5 years of experience in the pharmaceutical industry. Position: - QA Executive:- Education: MSc / BSc Experience: 4-6 years experience in Pharma Company Having good knowledge of QMS documentation like change ...

Hiring for Manager & Senior Manager Quality in Corrugated Boxes of 3 ply and 5 ply Manufacturing Industry Post : Senior Quality Manager Quality Manager Education: Any graduate / Engineering education background candidates should be preferred Experience: Min 10 Years in Corrugated Boxes Packaging Industries operating the quality management system & Integrated Management System (EMS & OHSAS), TPM, Kaizen, Writing procedures and processes to support the QMS development, internal auditing, ...

 B.E (Mechanical /Electrical/Instrumentation) with 6 to 10 years of experience in OSD pharma facility. Having Strong knowledge of o    Utility operations and maintenance o    Water system operations and maintenance o    HVAC operations and maintenance o     Requalification activities o     QMS documentation like SOP preparation, Change control, Qualification documentation preparation etc. Plant maintenance and calibration experience would be added advantages.      

Qualification: Diploma / BE in Mechanical, ProductionExperience: Min 10 to 15 yrs exp in Supply chain activities, Vendor development/improvement, PPAP & QMS documentation required.Work location: Greater Noida Job description:Drawing reading, feasibility & part cost confirmation, New Components development for Machining, Casting, Bending Automotive components. Identifying & developing new vendor/supplier for Machining, ...

IPQA activities, Plant round, Online BMR review, Line clearance, Samplingof APIs, Analytical data review, Batch release, APQR preparation. People who have faced regulatory audits like EDQM would be givenpreference.  Process & cleaning validation, including cleaning matrix preparation QMS documentation management; SOP preparation, review, and training IPQA activities to ensure GMP compliance during manufacturing. Regulatory inspection exposure ...