68 Job openings found

Position:          Executive/Asst. Manager - QA Location:         Silvassa Experience:      2 - 10 Years Industries:       Pharma Responsibilities:       Ensure compliance with GMP, regulatory guidelines, and quality standards in pharmaceutical formulation manufacturing. Manage quality systems, audits, documentation, validations, and batch release while leading the QA team. Implement and maintain Quality Management ...

Position:        QA Manager Location:        Ankleshwar Experience:     15 - 18 Years Industries:     Pharma - API   Responsibilities: Day to Day planning and execution of various activities in QA Execution/review/Approval & monitoring of process validation activities. Preparation, review, Approval of process validation Protocol/Report. Preparation, review and Approval of Annual Product Reviews Handling of Change Controls ...

Position:          QC Head  Location:         Jhagadia near by Ankleshwar  Experience:      10 - 15 Years Industries:       Pharma   Responsibilities:         Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards. To approve or reject, as he sees fit, raw materials, packing materials, semi finished product and finished products ...

Position:       QC Officer  Location:       Acchad nearby Bhilad Experience:   0 - 1 Years Industries:   Medical Devices Responsibilities: Individually handling department & manpower. Strong leadership skills to guide, supervise work activities, and help team members develop their skills. Work allocation / Planning and Review of documents. Preparation of SOP, Specification, Standard Test Procedures (STP), Raw Data ...

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 ...

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

Position:     Manager/Sr. Manager -QA Location:     Daman Experience:   10 to 16 Years Industries:     Pharma   Responsibilities: Qualification of Facility Approval of URS,SOP, Protocol & Report Approval of area layouts & equipment positioning layout Qualification of equipment’s Process validation Utility system validation HVAC system validation  Required Skills Greenfield Project Experience Excellent Communication   Required Qualification: - B.pharm/M.pharm Salary :- Upto 15.00 to  18.00  LPA If you are interested for this opening ...

Position:      QA/QC Specialist Location:      Umbergaon Experience:  6 - 7 Years Industries:  Medical Devices  Responsibilities: Quality Management System (QMS) Implement, maintain, and continuously improve the Quality Management System in accordance with CE, ISO 13485, ISO 9001, ISO 14001, ISO 45001, ISO/IEC 17025, and Indian MDR 2017 requirements. Ensure effective document control, change management, and ...

Position:      Design Engineer Location:      Umbergaon Experience:  3 - 6 Years Industries:  Medical Devices  Responsibilities: Product Design & Development   Design and develop hospital furniture and related products based on customer requirements and industry standards. Prepare 2D drawings, 3D models, assemblies, and manufacturing drawings. Develop product concepts and convert them into production-ready designs. Conduct design reviews and implement improvements ...

Position:     Sr. Executive - QA Location:      Silvassa Experience:   8 - 10 Years Industries:    Chemical   Responsibilities: Ensure compliance with Quality Management System (QMS) requirements. Prepare, review, and approve SOPs, specifications, formats, and quality documents. Handle deviations, CAPA, change control, incident investigations, and risk assessments. Conduct internal audits and coordinate external/customer audits. Monitor GMP, GLP, ISO, and ...