Average salary: Rs465,266 /yearly
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- Analytical Development Officer | Pharma | Vapi, Gujarat We are seeking a proactive and highly skilled Analytical Development Laboratory (ADL) Officer to join our team in Vapi, Gujarat. This full-time position offers a fantastic opportunity to contribute to the pharmaceutical...SuggestedFull time
- ...standard operating procedures (SOPs). Monitor in-process checks (IPC) and ensure compliance with quality standards. Coordinate with QA, QC, Engineering, and Warehouse departments for smooth production flow. Ensure proper documentation and compliance with USFDA, MHRA, and...Suggested
- ...performing team. BASIC REQUIREMENTS: Academic Qualifications: B.E./B.Tech. Chemical Job Experience: Minimum 15-20 years in Chemical/Pharma Company Technical Qualifications: SAP – MM module, MS Office etc. Job Location: Vapi (Gujarat) Other skills: Strong...SuggestedShift work
Rs 4 - 8 lakhs p.a.
...Quality Assurance Officer will act as a bridge between production and QC, ensuring manufacturing processes comply with internal and... ...~ M.Sc. in Chemistry. ~2+ years of experience in QA/QC within Pharma, Fine Chemical, or Cosmetic industries. ~ Knowledge of GMP documentation...Suggested- ...Global Operations Job Grade G10 Location : Dadra At Sun Pharma, we commit to helping you 'Create your own sunshine'— by fostering... ...practices in compliance with SOPs. Coordinate with QA, QC, Planning, and Engineering to ensure smooth batch execution and timely...SuggestedShift work
- ...Review and approve quality control data, test results, and inspection reports before product release. Coordinate with the Production and QC Testing teams to ensure timely resolution of non-conformities. 2. Process Validation and Documentation Prepare, execute, and...Suggested
- ...Support training initiatives related to documentation best practices. 6. Cross-Functional Coordination • Coordinate with RA, QA, QC, R&D, Manufacturing, and Validation teams for documentation related to IVF devices. • Support documentation for process validation, bench...Suggested
- ...feedback to engineering, manufacturing, and suppliers for quality improvement. 6. Documentation & Regulatory Compliance • Maintain QC documentation in line with ISO 13485 and CDSCO requirements. • Ensure accurate recording of inspection results, test data,...Suggested
- ...perspective. • Review inspection records and ensure compliance with engineering drawings and quality requirements. • Coordinate with QC teams for raw material inspection planning and execution. 4. Non-Conformance & Deviation Handling • Assist in documentation and...Suggested
- Job Title: Quality Control Engineer – Surgical Robotics. Department: Quality Control – Surgical Robotics. Location: Vapi, Gujarat. Reports To: Manager / Senior Manager – Quality Control. Job Purpose: To ensure the quality, safety, and compliance of...Suggested
- ...A pharmaceutical company in Vapi is seeking Executives in Production, QC, and Packing (Oral Liquid) . The ideal candidates will be responsible for overseeing various aspects of the production process, ensuring quality control, and managing packing operations. Responsibilities...SuggestedFull time
- ...3 to 6 Years Qualifications: B. Sc/ M. Sc- Organic Chem. Or B. Pharma / M. Pharma (Preferable) Location: Vapi - Gujarat Client is... ...of regulatory systems (e.g., UKMHRA, EMA, ANVISA CDSCO). • Prior QC/analytical lab experience (esp. with HPLC) is a plus. • Proficient...SuggestedPermanent employmentFull timeWorldwide
Rs 5 - 8.5 lakhs p.a.
...Track production output, machine efficiency, downtime, and wastage. Ensure product quality as per specifications and coordinate with QA/QC teams. Enforce adherence to SOPs, GMP, 5S, and safety standards on the shop floor. Maintenance & Process Management Coordinate...SuggestedShift work- ...Job Title: QC Testing Engineer – Radiology & Imaging Systems (X-Ray / C-Arm / DR / CT) Department: Quality Control / Quality Assurance – Radiology Division Location: Vapi, Gujarat Reports To: QC Supervisor / Manager – Radiology Systems Job Purpose:...Suggested
- ...transfer and process scale-up activities. Troubleshoot process deviations and assist in investigations. Work closely with Upstream, QA, QC, and Validation teams to ensure smooth batch execution. Maintain strict adherence to aseptic practices, safety guidelines, and...Suggested
- ...RIL HSE Management System HSE Policy, Principles, Standards and Procedures & Practices Emergency Preparedness and response Education Qualification-: B. Sc. Chemistry, Masters preferred Experience Required -: Minimum 5-7 years in QA/QC discipline...Shift work
- ...logbooks, and deviation reports. Train and guide operators on SOPs, equipment handling, and safety protocols. Coordinate with QA, QC, R&D, and engineering teams for validations, investigations, and new product introductions. Participate in audits, CAPA implementation...
- ...Informatics Location: Dadra Areas Of Responsibility At Sun Pharma, we commit to helping you 'Create your own sunshine' — by... ...compliance to all quality related, Policies, Standards and IT systems at QC of the site. Facilitate internal and regulatory agency audits,...
Rs 2.5 - 3.5 lakhs p.a.
...lab equipment, process instruments) and ISO certification/upgrade requirements. · Generate enquiries by meeting Owners, Plant Heads, QA/QC Heads, Maintenance and EHS teams. Explain company services: · Calibration scope and periodic calibration needs · ISO...Long term contractFull time- ...strip packing machines. Good leadership, communication, and problem-solving skills. Key Competencies Attention to detail and documentation accuracy. Ability to work under pressure and meet deadlines. Strong coordination with QA, QC, and Production teams....
- Should have worked in Managerial capacity in Pharmaceutical API Intermediate/CDMO manufacturing set ups Responsible for Daily Production activities as per the monthly plan Responsible for Yield and Quality improvement and it’s monitoring Responsible for RMC and productivity...Full time
- Job Responsibility & Accountability (Key Roles, functions & accountability): Perform inspections as and when assigned in accordance to Client and Bureau Veritas guidelines. Manage the operations of the station office (if assigned). Fully understand...Work at officeLocal area
- ...thickness, friability) and resolve deviations. Oversee equipment setup, cleaning, and preventive maintenance. Coordinate with QA/QC for line clearance and documentation accuracy. Handle changeovers and ensure timely completion of production schedules. Train and...Shift work
Rs 20 - 22 lakhs p.a.
...Management Reduce rejections, scrap and rework through robust quality controls and root cause analysis (RCA). Coordinate with QA/QC to implement corrective actions and maintain quality certifications. Monitor customer complaints and ensure timely resolution and preventive...Relocation- ...Managing timely commission of Green Field Project & manufacturing of Pharma Intermediates & API’s Products, its operations, production/... ...leading a direct team of functional managers (Production, Maintenance, QC & Engineering) and a team of plant operators. # Will be...For contractors
- IT DESKTOP SUPPORT ENGINEER PHARMA Start Date Starts Immediately CTC (ANNUAL) Competitive salary Competitive salary Experience...Immediate start
- ...in Daman. The ideal candidate will have a strong background in aseptic filling, QMS, and plant maintenance, with expertise in QA, IPQA, QC, and microbiology. 1. Production – Aseptic Filling (Injectable) Experience: 4–8 Years Qualification: B.Pharm / M.Pharm / B.Sc / M....Full time
Rs 4.5 - 8 lakhs p.a.
...internal and external audits and implement corrective actions. Ensure adherence to statutory and regulatory requirements applicable to pharma packaging. Maintain high product quality standards meeting customer specifications. Operational Excellence & Continuous...Rs 2.5 - 4.5 lakhs p.a.
• Supervise manufacturing processes ensuring adherence to quality control standards • Monitor raw material usage and maintain batch consistency • Conduct routine testing of raw materials, in-process products, and finished goods • Collaborate with Quality Assurance team...- ...activities including URS, FRS, HDS, RA, IQ, OQ, PQ, and Validation Summary Reports (VSR). Perform validation of manufacturing, packing, QC, and utility systems (PLC/SCADA/DCS, EMS/BMS, LIMS, ERP, QMS, chromatography systems, CSV‑related equipment). Ensure compliance with...
