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)
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)
2.0 Year(s) To 5.0 Year(s)
5.00 LPA TO 7.00 LPA
Position: Maintenance Engineer
Location: Vapi
Experience: 2 - 5 Years
Industries: Pharma - API
Responsibilities:
Core Documentation Responsibilities
Equipment & Facility Documentation
Maintain and control engineering drawings, P&IDs (Piping & Instrumentation Diagrams), equipment manuals, and spare parts lists
Manage equipment qualification documents (IQ, OQ, PQ) and requalification schedules
Create and update equipment files, ...
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)
3.0 Year(s) To 7.0 Year(s)
2.00 LPA TO 4.50 LPA
📌 Key Responsibilities
Handle day-to-day API production operations as per BMR/BPR and SOPs.
Operate and monitor reactors, centrifuges, dryers, filters and other process equipment.
Execute batch manufacturing activities as per approved procedures.
Monitor critical process parameters and ensure batch yield and quality.
Maintain proper production documentation and ensure ALCOA+ compliance.
Follow cGMP, SOP, EHS and safety ...
1 Opening(s)
4.0 Year(s) To 7.0 Year(s)
5.00 LPA TO 6.00 LPA
A Quality Assurance (QA) Assistant Manager for a starch powder or pharmaceutical/food-grade starch active/derivative manufacturing plant in the Dhule/Dondaicha MIDC region oversees cGMP compliance, QMS documentation, process validation, and regulatory audits for specialized grades (IP, BP, USP).
Job Profile & Core Details
Position Title: Assistant Manager - Quality Assurance (QA)
Industry Segment: ...
1 Opening(s)
1.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 4.00 LPA
Position: Officer/Executive - Packing
Location: Daman
Experience: 1 - 8 Years
Industries: Pharma
Responsibilities:
To finalize Packing plan for weekly and monthly.
To allocate work to workforce and perform the critical checks and ensure line clearance at all stages of Packing to implement Current good manufacturing practice.
Preparation and ...
1 Opening(s)
18.0 Year(s) To 25.0 Year(s)
40.00 LPA TO 50.00 LPA
Position: Production Head
Location: Bhopal
Experience: 18 – 25 Years
Industries: Pharma
Responsibilities:
Lead end-to-end production operations for biologics, sterile injectables, formulation & fill-finish activities.
Ensure compliance with cGMP, GDP, aseptic practices & data integrity requirements.
Drive production planning, process optimization, technology transfer & commercial scale-up activities.
Ensure manufacturing readiness for global regulatory inspections including USFDA, ...
1 Opening(s)
6.0 Year(s) To 8.0 Year(s)
Not Disclosed by Recruiter
Designation – Process - Equipment ( OSD)
Qualification – BE Mechanical/ Chemical
Work Timings – 9 hours
Working Days – Monday to Saturday
Work Location – Pithampur
Salary (Min & Max) – Best in industry
Experience – 5+ years
Benefits - On duty Lunch, PF, Mediclaim, Paid leaves
Note: This role will be on payroll of Talisman HR SolutionsAuto renewable contract based ...