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- Documentation Executive Start Date Starts Immediately CTC (ANNUAL) Competitive salary Competitive salary Experience...SuggestedImmediate start
- ...quality standards. Coordinate with QA, QC, Engineering, and Warehouse departments for smooth production flow. Ensure proper documentation and compliance with USFDA, MHRA, and other regulatory guidelines. Train and guide operators and technicians on GMP practices and...Suggested
- ...Operations Job Grade G10 Location : Dadra At Sun Pharma, we commit to helping you 'Create your own sunshine'— by fostering... ...ongoing cost optimization projects. GMP Compliance & Documentation Ensure strict adherence to cGMP, data integrity (ALCOA+), and...SuggestedShift work
- ...Affairs Job Grade G12A/G12B Location Dadra At Sun Pharma, we commit to helping you ' Create your own sunshine '— by... ...process qualification batches To prepare and review new product documents like material requirement sheet, master formula card, bill of material...Suggested
- 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
- ...Department Review the filled BPR after completion of batch Review the BPR, SOP, validation protocol, and other production related documents Initiation of change control for any change in production related activities Evaluate, investigate, and report critical...SuggestedFull time
- ...Job Grade G9B Location : Mumbai or Baroda At Sun Pharma, we commit to helping you 'Create your own sunshine'— by fostering... ...certificates of analysis/compliance and all related supporting documentation (i.e. documentation review, SOP compliance, instrument...Suggested
- ...and other applicable regulatory guidelines . Maintain proper documentation (GRN, Material Issue Slip, Stock Register, Bin Cards, etc.).... ...documentation practices, and audit compliance. ~ Experience working with ERP systems (SAP / Oracle / Tally ERP / Pharma ERP)....Suggested
- ...Coordinate and plan with various cross functional areas to ensure successful implementation of ideas. Ensure compliance with company & industry standards. Any other work assigned by management from time to time. Required Experience: 2-6 years in Pharma, API...Suggested
Rs 7 - 9.5 lakhs p.a.
...reports and recommend corrective actions to prevent recurrence. Maintain records related to EHS activities, audits, and compliance documentation. Liaise with regulatory bodies, ensuring all EHS statutory requirements are met timely and accurately. Support emergency...SuggestedFor contractors- ...& Compliance Job Grade G8 Location : Dadra At Sun Pharma, we commit to helping you 'Create your own sunshine'— by fostering... ...Implementing various safety measures to minimize incidents and documenting conceptual details through monthly safety meetings. In charge...Suggested
- ...Coordination Responsibilities: Communicating drawings and material requirements to the site execution team Planning and documentation for material dispatch Attending client meetings, providing support, and resolving site queries Tracking project progress...Suggested
- ...To support and execute clinical studies, trials, and observational research activities while developing high-quality clinical documentation, scientific outputs, and regulatory-ready evidence. The role contributes to patient safety, product credibility, and scientific excellence...SuggestedImmediate start
- ...breakdown of any equipment in the manufacturing facility. Manufacturing of CAR-T cells in cGMP environment and preparation of related documents as per quality compliance. Coordination with QC for sharing of In-process and final product samples and preparation of associated...SuggestedShift work
- ...AERB licensing for manufacturing, installation, and servicing of X-Ray, C-Arm, DR, and CT systems. Prepare, maintain, and submit documentation required for AERB, NABL, and ISO 13485 compliance. Liaise with regulatory authorities for approvals, renewals, audits, and...Suggested
- ...Gujarat Reports To: Manager / Senior Manager – Regulatory & Safety Job Purpose: To manage and coordinate regulatory documentation and compliance activities for radiology and imaging systems such as X-Ray, C-Arm, Digital Radiography (DR), and CT equipment...Work at office
- ...requirements. Ensure procurement activities comply with company policies, procedures, and statutory guidelines. Maintain proper documentation related to procurement transactions. Support internal and external audits related to procurement activities and close audit...
- ...Assurance system for surgical robotic products by ensuring compliance with ISO 13485, internal SOPs, and regulatory requirements through documentation control, process adherence, non-conformance handling, and coordination with cross-functional teams. Key Responsibilities: 1...
Rs 2 - 4 lakhs p.a.
Corporate Sales Executive Start Date Starts Immediately CTC (ANNUAL) ₹ 2,00,000 - 4,00,000 ₹ 2,00,000 - 4,00,000 /year ...Immediate startRs 20 - 22 lakhs p.a.
Job Title: Assistant General Manager - Production (Laminates / Panels) Location: Sarigam, Gujarat (near Vapi). Candidate must be willing to relocate to Sarigam. Industry Preference: Laminates / Furniture Panels / MDF / Particle Board / Modular Furniture Boards Reporting...Relocation- ...TFF systems, AKTA chromatography skids, depth filters, and associated single-use technologies. Monitor critical process parameters and document activities in real time following GDP practices. Support technology transfer and process scale-up activities. Troubleshoot process...
- Job Title: Plant Chemist (more than 1-5 years of experience) Qualifications- Bsc Chemistry/Diploma/ B E Chemical Company Overview: We are a dynamic and rapidly growing chemical manufacturing company specializing in hydrogenation, chlorination, reduction, distillation,...
Rs 6 - 10 lakhs p.a.
Key Responsibilities: Drive B2B sales for Pre-Engineered Steel Buildings, Metal Roofing Systems, Heavy Steel Structures, and Industrial Infrastructure solutions. Develop and manage relationships with corporate, institutional, and industrial clients. Identify new business...- ...developing alternate feedstock/raw material in coordination with the business group. Coordinate completion of applicable statutory documents and compliance. Monitor prices of raw materials, products, fuels & utilities etc. to identify profit maximization opportunities....
- ...by following internal and external SOPs, Work Instructions and Forms/Templates for successful preparation of robust CERs and other documents Assisting with other clinical, regulatory, quality and engineering projects as assigned Responsible to acquire, interpret, analyze...Full time
- Roles and Responsibilities: Prepare detailed production and supply plans for forming, processing, and subcontracted operations on a weekly, monthly, and annual basis to ensure timely fulfilment of customer demand. Coordinate daily with the production team to review production...
- ...desirable. Key Competencies Strong experimental and analytical skills Ability to design and optimize biological assays Strong documentation and scientific reporting skills Ability to work in a collaborative research environment Earn certifications in these...Immediate start
Rs 2.5 - 3.5 lakhs p.a.
...Maintenance and EHS teams. Explain company services: · Calibration scope and periodic calibration needs · ISO implementation, documentation and audit support · AMC / annual calibration and certification packages. · Coordinate with internal technical team to prepare...Long term contractFull timeRs 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...- ...surgical robotic products by ensuring effective implementation of the ISO 13485 Quality Management System, regulatory compliance, robust documentation practices, and proactive quality risk management across manufacturing, inspection, and support processes. Key...
