1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
9.00 LPA TO 10.00 LPA
Position: QA Executive
Location: Daman
Experience: 8 - 10 Years
Industries: Pharma
Responsibilities:
Ensure compliance with cGMP, GLP, SOPs and regulatory requirements.
Review and approve BMR/BPR, SOPs, specifications and quality documents.
Handle Deviations, OOS/OOT, CAPA, Change Control and investigations.
Monitor QA activities across manufacturing and ensure GMP compliance.
Conduct and support internal, customer and ...
1 Opening(s)
18.0 Year(s) To 20.0 Year(s)
16.00 LPA TO 18.00 LPA
Position: QC Head
Location: Daman
Experience: 18 - 20 Years
Industries: Pharma
Responsibilities:
Lead and manage the overall Quality Control function and QC laboratory.
Ensure compliance with cGMP, GLP, ICH, WHO and regulatory requirements.
Oversee testing and release of raw materials, packing materials, in-process and finished products.
Review and approve specifications, analytical reports, SOPs, ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: QC Executive
Location: Silvassa
Experience: 2 - 6 Years
Industries: Pharma
Responsibilities:
Perform sampling and testing of raw materials, in-process and finished products.
Conduct chemical/physical analysis as per SOPs and specifications.
Maintain QC records, logbooks, worksheets, and test reports.
Operate and maintain laboratory instruments and equipment.
Handle OOS/OOT investigations and support CAPA activities.
Ensure compliance ...
1 Opening(s)
0 To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: Officer/Executive - QC
Location: Silvassa
Experience: 0 - 5 Years
Industries: Pharma
Responsibilities:
Perform raw material, in-process, finished product, and packaging material testing.
Conduct chemical and physical analysis as per specifications and SOPs.
Prepare and maintain analytical records and laboratory documentation.
Operate and maintain laboratory instruments (HPLC, GC, UV, pH ...
1 Opening(s)
6.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 8.00 LPA
Position: Dy. Manager - QC
Location: Vapi
Experience: 6 - 8 Years
Industries: Pharma - API
Responsibilities:
Manage day-to-day Quality Control activities for raw materials, intermediates, APIs, finished products, and stability samples.
Ensure compliance with cGMP, GLP, ICH, FDA, EU GMP, and regulatory requirements.
Review and approve analytical test results, ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 5.00 LPA
Responsibilities: QA Executive
To assign control number of Change control, Deviation, CAPA, OOS, OOT etc.
To handle QMS related documents and its applicable Quality trends.
To review investigation reports for deviation, OOS, OOT, OOE & Market Complaint.
To coordinate for Internal Audit.
To Issue and retrieve of Batch Production Record and Equipment Cleaning Record for ...
1 Opening(s)
7.0 Year(s) To 10.0 Year(s)
6.00 LPA TO 8.00 LPA
Position: Sr. Executive - QA
Location: Bhimpore - Daman
Experience: 7 - 10 Years
Industries: Medical Device
Responsibilities:
Preparation, coordination, and successful handling of audits from USFDA, MHRA, WHO-Geneva, and other regulatory authorities.
Review and compilation of documents required for regulatory inspections.
Preparation of ...
1 Opening(s)
10.0 Year(s) To 20.0 Year(s)
10.00 LPA TO 12.00 LPA
Key Responsibilities
Quality Control Operations
Overall responsibility for raw material, in-process, and finished product testing
Ensure timely analysis and release of materials and products
Review and approve COAs (Certificates of Analysis)
Ensure adherence to approved specifications and SOPs
Laboratory Management
Manage QC laboratory operations, manpower, and workflow
Ensure proper calibration, validation, and maintenance of laboratory instruments
Control and monitoring ...
1 Opening(s)
3.0 Year(s) To 8.0 Year(s)
Not Disclosed by Recruiter
The job description is as below:
Purpose of the RoleTo ensure timely, accurate, compliant, and scientifically justified responses to regulatory and customer queries related to pharmaceutical and medical device testing, in alignment with global regulatory and accreditation requirements.
Key Responsibilities
1. Regulatory Query ManagementReceive, log, track, and respond to regulatory queries, including US ...
1 Opening(s)
20.0 Year(s) To 30.0 Year(s)
Not Disclosed by Recruiter
Minimum 20 years in Quality Assurance/Quality Systems in API/pharmaceutical manufacturing, with significant exposure to regulated markets
To provide strategic and operational leadership to the Quality function, ensuring robust implementation of quality systems, compliance with global regulatory requirements, and continuous improvement in all quality-related processes for API manufacturing.
Key Responsibilities
Quality Systems & Compliance
Implement, ...