1 Opening(s)
12.0 Year(s) To 15.0 Year(s)
25.00 LPA TO 30.00 LPA
Position: QA Manager
Location: Ahmedabad
Experience: 12 - 15 Years
Industries: Pharma
Responsibilities:
Ensure compliance with GMP, regulatory guidelines, and quality standards in pharmaceutical formulation manufacturing.
Manage quality systems, audits, documentation, validations, and batch release while leading the QA team.
Implement and maintain Quality Management Systems (QMS) as per USFDA, WHO-GMP, ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
20.00 LPA TO 25.00 LPA
Position: AGM/DGM - ADL
Location: Mundra
Experience: 10 - 15 Years
Industries: Chemicals
Responsibilities:
Responsible for a analytical team in method development, method transfer and validation of various stages of product development.
Develop testing method by GC, HPLC, GCMS etc and interpretation of analytical data.
Develop testing wet ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
Position: QC Manager
Location: Vapi
Experience: 8-10 YEARS
Industries: Pharma
Responsibilities:
Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards.
To approve or reject, as he sees fit, raw materials, packing materials, semi finished product and finished products as per agreed/approved ...
1 Opening(s)
10.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 20.00 LPA
Position: QC Manager
Location: Ahmedabad
Experience: 10 - 12 Years
Industries: Pharma - Formulation Responsibilities:
Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards.
To approve or reject, as he sees fit, raw materials, packing materials, semi-finished product and finished products ...
2 Opening(s)
5.0 Year(s) To 10.0 Year(s)
7.00 LPA TO 9.00 LPA
Position: Executive/Sr. Executive - QC
Location: Daman
Experience: 5 - 10Years
Industries: Pharma
Responsibilities:
Individually handling department & manpower.
Strong leadership skills to guide, supervise work activities, and help team members develop their skills.
Work allocation / Planning and Review of documents.
Preparation of SOP, Specification, Standard Test Procedures ...
2 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.50 LPA
Position: QA - Officer
Location: Silvassa
Experience: 2 – 5 Year
Industries: Pharma
Responsibilities:
Line clearance prior to Dispensing, Manufacturing, and Packaging and Validation activity.
In process check during batch manufacturing and packing as per the instructions and frequency given in the ...
2 Opening(s)
4.0 Year(s) To 7.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: Microbiologist Officer
Location: Daman
Experience: 4 - 7 Years
Industries: Pharma
Responsibilities:
Microbiological Testing: Perform microbiological tests (sterility, microbial limit tests) on raw materials, in-process samples, and finished products.
Environmental Monitoring: Conduct routine environmental monitoring of cleanrooms, aseptic areas, and production zones, ensuring microbial control limits are met.
Aseptic Process ...
7 Opening(s)
6.0 Year(s) To 7.0 Year(s)
5.00 LPA TO 10.00 LPA
Position: Asst. Manager - QA
Location: Daman
Experience: 6 - 7 Years
Industries: Pharma
Responsibilities:
Shall be Responsible for ensuring Good Laboratory Practices compliance in Quality Control department.
Handling of out of Specification (OOS), Out of Trend (OOT), Out of Calibration (OOC) and Lab Event investigations.
Sporadic Review of stability. PM, ...
1 Opening(s)
1.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: Officer/Sr. Officer - IPQA
Location: Daman
Experience: 1 - 4 Years
Industries: Pharma
Responsibilities:
Review and approve batch records, laboratory data, and other relevant documents related to the manufacturing process.
Ensure all operations comply with GMP guidelines and internal quality standards.
Conduct internal audits to assess adherence to GMP, standard operating procedures ...
1 Opening(s)
6.0 Year(s) To 8.0 Year(s)
4.20 LPA TO 6.00 LPA
Position: Sr. Executive/Asst. Manager - QA
Location: Panoli - Ankleshwar
Experience: 6 - 8 Years
Industries: Pharma - API
Responsibilities:
Review and approve batch records, laboratory data, and other relevant documents related to the manufacturing process.
Ensure all operations comply with GMP guidelines and internal quality standards.
Conduct internal audits ...