1 Opening(s)
10.0 Year(s) To 12.0 Year(s)
12.00 LPA TO 13.00 LPA
Position: Asst./Dy. Manager - Production
Location: Vapi
Experience: 10 - 12 Years
Industries: Pharma - API
Responsibilities:
Oversee day-to-day API manufacturing operations (batch/continuous processes).
Ensure strict compliance with cGMP, USFDA, MHRA, WHO, and other regulatory standards.
Review and execute Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
Coordinate with QA/QC to ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
12.00 LPA TO 13.00 LPA
Position: Dy. Manager - Quality
Location: Vapi
Experience: 8 - 10 Years
Industries: Pharma API
Responsibilities:
Quality Management System (QMS)
Establish, implement, and maintain an effective Quality Management
System in line with cGMP, ICH, USFDA, EU-GMP, WHO, and other regulatory requirements.
Ensure compliance with SOPs, policies, and ...
1 Opening(s)
12.0 Year(s) To 18.0 Year(s)
20.00 LPA TO 25.00 LPA
Position: Sr. Manager - QC
Location: Ahmedabad
Experience: 12 - 18 Years
Industries: Pharma
Responsibilities:
Lead and oversee the entire Quality Control department operations.
Ensure compliance with cGMP, regulatory guidelines, and company quality standards.
Review and approve analytical methods, specifications, and validation protocols.
Supervise raw material, in-process, and ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: QA Officer
Location: Vapi
Experience: 3 - 4 Years
Industries: Pharma API
Responsibilities:
Review QC raw data, BMRs, STPs, and specifications.
Monitor compliance with cGMP, GLP, and documentation practices.
Conduct GMP training sessions and maintain related records.
Handle deviations, change control, CAPA, and non-conformance.
Perform self-inspections, audits, and ensure ISO ...
1 Opening(s)
11.0 Year(s) To 12.0 Year(s)
14.00 LPA TO 15.00 LPA
Position: Maintenance Manager
Location: Khopoli
Experience: 11 - 12 Years
Industries: Pharma
Responsibilities:
Planning and execution of maintenance activities.
Utility Log sheet monitoring.
Co- ordination with all departments pertaining to maintenance activity.
Review utility consumption report on daily / monthly basis.
Preventive maintenance of all the equipment monitoring.
Ensure calibration of ...
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)
6.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: Sr. Officer - IPQA
Location: Bhimpore - Daman
Experience: 6 - 8 Years
Industries: Medical Device
Responsibilities:
IPQA (In-Process Quality Assurance) Monitoring
Supervise and monitor all IPQA activities in manufacturing areas.
Ensure compliance with cGMP guidelines during production processes.
Line clearance verification before batch ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
2.00 LPA TO 4.00 LPA
Position : Production Officer (Documentation)
Location : Vapi
Experience: 2- 3 Years
Industries: Pharma - API
Responsibilities:
Coordinate with QA, QC, Purchase, and Warehouse for smooth production flow.
Monitor raw material usage, yield efficiency, and finished product quality.
Maintain cGMP compliance in all production operations and documentation.
Ensure shift-wise presence and manage production ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: Executive - Utility & Maintenance
Location: Vapi
Experience: 4 - 6 Years
Industries: Pharma API
Responsibilities:
Planning and execution of routine maintenance activities.
Check utility daily Log sheet.
Co- ordination with all departments pertaining to maintenance activity.
Carry out all the maintenance activities as ...
1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 5.50 LPA
Position: QA Officer
Location: Sarigam Near By Vapi
Experience: 3 - 6 Years
Industries: Chemical
Responsibilities:
Ensure current versions of all GMP documents are in use across departments.
Prepare, revise, and control SOPs and related quality documents.
Implement and enforce Good Documentation Practices (GDP).
Prevent retention of obsolete ...