561 Job openings found

1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 3.60 LPA
A Sr. Chemist QC (Quality Control) analyzes raw materials, in-process samples, and finished products using advanced techniques (HPLC, GC) to ensure quality, consistency, and regulatory compliance (GMP, ISO), requiring strong analytical skills, documentation, equipment management, and leadership to mentor junior staff and resolve complex quality issues. Key duties involve developing SOPs, ...
1 Opening(s)
5.0 Year(s) To 7.0 Year(s)
8.00 LPA TO 9.00 LPA
Position:        Shift Incharge - Production Location:        Bhilad - Vapi Experience:     5 - 7 Years Industries:      Cosmetics Responsibilities: Supervise daily production activities for cosmetic and personal care products such as creams, lotions, shampoos, soaps, and face washes. Manage batch preparation, raw material dispensing, mixing, heating, homogenization, and filling ...
1 Opening(s)
12.0 Year(s) To 20.0 Year(s)
Not Disclosed by Recruiter
Designation - Manager E&M Mechanical Working Days - Mon to Fri & Alternate Sat working Work timing - 9:30 to 5:30 Payroll - Offrole contractual role (Contract is auto-renewable) Job Description: Responsible for Maintenance & modification works of API Plant equipment.  Need to maintain uptime of plant equipment to meet production targets. Responsible for investigation and CAPA ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 6.00 LPA
Role OverviewThe MEP Design Engineer will support the planning and design of pharmaceutical cleanrooms and associatedbuilding services, ensuring that layouts and engineering systems meet project requirements, applicablestandards, and GMP expectations. Key Responsibilities Develop and review MEP design deliverables for pharmaceutical projects, with a focus on cleanroom andcontrolled-environment facilities. Prepare and coordinate ...
1 Opening(s)
8.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 15.00 LPA
Key Responsibilities: Ensure compliance with cGMP, GLP, FDA and regulatory requirements. Lead QC team operations, daily task allocation and technical troubleshooting. Review analytical raw data, HPLC/GC audit trails, SOPs and batch release documents. Lead investigations related to OOS, OOT, deviations and incidents, including RCA and CAPA. Manage stability studies, instrument calibration, analytical method validation/transfer and ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
4.00 LPA TO 5.50 LPA
Position:        QC Executive Location:      Bhilad nearby Vapi Experience:    3 - 4 Years Industries:     Cosmetic  Responsibilities: Supervising in-process quality control and managing bulk approvals and finished goods (FG) release. Hands-on experience in instrumental and analytical testing of raw materials (RMs). Identifying quality-related issues and implementing effective solutions to mitigate them. Maintaining comprehensive ...
1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 6.00 LPA
Position:        Manufacturing Executive Location:       Bhilad nearby Vapi Experience:    3 - 6 Years Industries:     Cosmetic Responsibilities: Bulk Manufacturing Operations: Execute Planning and monitor bulk manufacturing processes including Raw material Handling, weighing, mixing, blending, and batch preparation as per approved formulas and SOPs. Ensure production targets and batch schedules are completed ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
3.50 LPA TO 4.00 LPA
Position:      Production Officer ( Documentation ) Location:      Daman Experience:  1 - 5 Years Industries:    Pharma Responsibilities: Monitor and control daily production activities as per production plan. Ensure manufacturing of tablets, capsules, syrups, or other formulations as per SOPs and GMP guidelines. Supervise machine operation, line clearance, and production manpower. Maintain batch manufacturing records ...
1 Opening(s)
5.0 Year(s) To 7.0 Year(s)
7.00 LPA TO 7.20 LPA
Position:         QC Officer Location:         Dadra Experience:     5 - 7 Years Industries:     Chemical - MNC Responsibilities: Perform quality inspections of raw materials, in-process products, and finished goods. Conduct routine testing and measurements according to standard procedures. Record and maintain quality control data and reports. Identify quality issues and report deviations to ...
1 Opening(s)
8.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 15.00 LPA
Key Responsibilities: Ensure compliance with cGMP, GLP, FDA and regulatory requirements. Lead QC team operations, daily task allocation and technical troubleshooting. Review analytical raw data, HPLC/GC audit trails, SOPs and batch release documents. Lead investigations related to OOS, OOT, deviations and incidents, including RCA and CAPA. Manage stability studies, instrument calibration, analytical method validation/transfer and ...

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