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- Research and develop new medical devices based on market requirements. Identify opportunities for new product development and innovation. Develop product concepts, designs, specifications, and prototypes. Conduct feasibility studies for new product development. ...SeniorFull time
- ...Notebook. The applicant will have an excellent practical and theoretical understanding of synthetic organic chemistry or a relevant technology and can design and execute high-quality, thoughtful experimentation while making significant contributions both independently and as...SuggestedFull timeShift work
- ...wiring diagrams, and hook-up drawings . Perform loop checking and assist with commissioning activities. Check 4–20 mA, 24 VDC, digital signals, and analogue I/O . Follow plant safety procedures, permit-to-work systems, and maintenance standards . Maintain...DigitalFull time
- QA-Manager Criteria: B Tech (Chemical, Food, Cosmetics) with minimum 3 to 7 years of experience as QA head in cosmetics/ FMCG industry 1. Quality System Oversight o Develop, implement, and maintain GMP (Good Manufacturing Practices) and ISO standards for cosmetics production...SuggestedFull time
Rs 15 - 17 lakhs p.a.
Senior Manager, Procurement Department: Procurement & Supply Chain Location: Vapi, Gujarat Experience: 12–15 years CTC budget: 15–17 LPA Employment type: Full-time Industry: Real Estate, Construction, Engineering Job Summary Manage procurement ...SeniorFull timeContract work- Key Responsibilities Execute day-to-day manufacturing of urology medical devices. Prepare and maintain Batch Manufacturing Records (BMR) and production documentation. Ensure compliance with ISO 13485, GMP, and company Quality Management System. Coordinate with...SeniorFull time
- Implement and monitor workplace Health, Safety, and Environment (EHS) policies, procedures, and practices to ensure a safe working environment. Ensure effective implementation of fire safety measures , including fire prevention, fire protection systems, firefighting equipment...SeniorFull timeFor contractors
- 0-2 year experience in Medical Device/Pharma industry. Job Responsibility - Monitoring of qualification and validation activities. - Preparation of technical files and related documentation. - Preparation and review of qualification & validation protocols and reports...SeniorFull time