64 Job openings found

1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 12.00 LPA
Position:       QA Manager Location:       Daman Experience:   8 - 10 Years Industries:    Packaging Responsibilities: Develop and maintain Quality Management System (QMS) as per ISO/BRC standards Conduct internal and external quality audits Approve and inspect incoming raw materials (resins, additives, inks) Monitor production processes (extrusion, printing, lamination, slitting) Ensure calibration and maintenance of testing equipment Define and ...
1 Opening(s)
20.0 Year(s) To 25.0 Year(s)
18.00 LPA TO 22.00 LPA
Good Knowledge of USFDA/ EDQM /ANVISA / and all other regulatory & CGMP awareness. Strategic oversight and leadership: Develop and implement the company's quality management system (QMS) and strategy, aligning it with business objectives. This includes overseeing all aspects of quality operations and managing the QA and QC departments. Regulatory compliance: Ensure ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
5.00 LPA TO 7.00 LPA
Quality Assurance Specialist Responsibilities: Ensure product quality and conformity to regulatory standards, including Medical Device Regulation (MDR) and Quality Management System (QMS). Conduct internal quality audits and participate in management review meetings. Handle investigations of complaints and implement corrective and preventive actions. Maintain and update quality manuals, formats, and standard operating procedures (SOPs) in ...
10 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 8.00 LPA
🔬 Quality Testing & Analysis Perform routine and non-routine chemical analyses on raw materials, in-process samples, and finished goods using standard laboratory methods. Operate and validate analytical instruments such as HPLC, GC, UV-Vis, FT-IR, Karl Fischer titrator and other relevant equipment. Record, calculate, interpret and report accurate analytical results, ensuring data integrity and ...
10 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 8.00 LPA
🔬 Quality Testing & Analysis Perform routine and non-routine chemical analyses on raw materials, in-process samples, and finished goods using standard laboratory methods. Operate and validate analytical instruments such as HPLC, GC, UV-Vis, FT-IR, Karl Fischer titrator and other relevant equipment. Record, calculate, interpret and report accurate analytical results, ensuring data integrity and ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
2.40 LPA TO 2.64 LPA
  02.02.26 125475 HPS/2026/90 Quality Supervisor Male 1 2 to 3 BA/BCOM 10 Hours/9 to 7 PM A Quality Supervisor oversees a company's quality assurance/control department, ensuring products or services meet safety, industry, and customer standards Key Responsibilities- Inspection & Monitoring: Supervise daily QC inspectors and monitor production lines to identify defects in materials and finished products. Quality Management System (QMS): Develop, document, and maintain quality ...
1 Opening(s)
10.0 Year(s) To 20.0 Year(s)
15.00 LPA TO 20.00 LPA
• To review the maintenance of analytical instruments, facilities, records, anddocuments.• To review validation activities, including analytical test procedures, instruments, andcalibration of control equipment.• To ensure that initial and ongoing training of Quality Control personnel is conductedas per requirements.• To update final product specifications in line with statutory requirements.• To ...
1 Opening(s)
10.0 Year(s) To 20.0 Year(s)
8.00 LPA TO 11.00 LPA
Develop, implement, and maintain the Quality Management System (QMS). Ensure compliance with standards API product specification requirements related to quality control. Follow management of change, risk assessment and management and contingencies procedures for his function and maintain applicable records for his function as defined in the procedures Lead internal and external audits, including ...
5 Opening(s)
1.0 Year(s) To 6.0 Year(s)
Not Disclosed by Recruiter
Responsibilities Perform and supervise In-Process Quality Assurance (IPQA) OR QA checks during API manufacturing operations. Conduct on-line review of Batch Production Records (BPR) and ensure adherence to approved procedures. Ensure sampling, line clearance, and process compliance as per GMP/cGMP norms. Identify, record, and support resolution of deviations, non-conformances, and quality incidents during manufacturing. Support quality investigations and prepare required ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
4.80 LPA TO 7.20 LPA
12.02.26 20306 HPS/2026/132 Senior QC Chemist Male/Female 1 5 to 10 BSc/MSc 8 Hours Senior QC ChemistBudget – 40-60 k JOB DESCRIPTION-Responsible for ensuring that the quality management system (QMS) is fully implemented and followedDevelop test procedures with the help of R&D and upgrade all test facilities as per demanding requirementof customersCoordinate with external agencies for joint testingMaintain all records ...

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