30 Job openings found

Position:       QA Officer  Location:       Acchad nearby Bhilad Experience:   1 - 2 Years Industries:   Medical Devices Responsibilities: Review QC raw data, BMRs, STPs, and specifications. Monitor compliance with cGMP, GLP, and documentation practices. Conduct GMP training sessions and maintain related records. Handle deviations, change control, CAPA, and non-conformance. Perform self-inspections, audits, and ensure ISO compliance. Familiarity with ...

Position:    Maintenance Executive (Documentation) Location:        Vapi Experience:    1 - 3 Years Industries:     Pharma - API Responsibilities: Documentation Management Prepare, review, and maintain maintenance-related documents such as: Standard Operating Procedures (SOPs) Preventive Maintenance (PM) schedules Breakdown maintenance records Equipment history cards Maintenance logbooks Calibration records Utility maintenance records Control issuance, revision, archival, and retrieval of engineering documents. Compliance & Regulatory ...

Position:        R&D Engineer Location:       Kalol - Gandhinagar Experience:    2 - 3 Years Industries:     Engineering Responsibilities:  Work on projects with the concurrent support and instructions from the manager as per the project plan. Each design shall incorporate relevant codes and standards as well safety requirements during design stage and legible in ...

Position:        Plant Head (Bhopal) Location:       Bhopal Experience:   20 - 25 Years Industries:    Pharma Responsibilities: Lead end-to-end technical operations including biologics manufacturing, sterile injectables, formulation & fill-finish. Drive cGMP compliance, data integrity, technology transfer, process optimization & commercial scale-up. Ensure readiness for global regulatory inspections including USFDA, EU GMP, MHRA, WHO, ANVISA etc. Oversee plant administration, ...

Position:        Design & Development Officer Location:       Daman Experience:   2 - 3 Years Industries:    Pharma Responsibilities:         Design and develop mechanical equipment/components using AutoCAD, Solid Edge, and SolidWorks, ensuring compliance with GMP, cGMP, ISO, and FDA standards. Prepare detailed 2D/3D drawings and models as per ASME/IS standards and software-based design practices. Utilize design ...

Position:      Asst. Manager/Manager - QA Location:      Kadi - Ahmedabad  Experience:   5 - 7 Years Industries:    Pharma Responsibilities: Quality Assurance & Compliance Ensure compliance with cGMP, GLP, and regulatory requirements (WHO, USFDA, MHRA, etc.) Handle audits (internal, external, regulatory) and ensure audit readiness at all times Review and approve SOPs, BMRs, BPRs, protocols, and reports Documentation Management Oversee ...

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:         QA Officer Location:        Vapi Experience:     3 - 4 Years Industries:      Pharma API   Responsibilities: Review QC raw data, BMRs, STPs, and specifications. Monitor compliance with cGMP, GLP, and documentation practices. Conduct GMP training sessions and maintain related records. Handle deviations, change control, CAPA, and non-conformance. Perform self-inspections, audits, and ensure ISO ...

Position:         Maintenance Manager Location:        Khopoli Experience:     11 - 12 Years Industries:      Pharma  Responsibilities: Planning and execution of maintenance activities. Utility Log sheet monitoring. Co- ordination with all departments pertaining to maintenance activity. Review utility consumption report on daily / monthly basis. Preventive maintenance of all the equipment monitoring. Ensure calibration of ...

Position:          Sr. Executive - QA Location:          Bhimpore - Daman Experience:       7 - 10 Years Industries:        Medical Device Responsibilities: Preparation, coordination, and successful handling of audits from USFDA, MHRA, WHO-Geneva, and other regulatory authorities. Review and compilation of documents required for regulatory inspections. Preparation of ...