1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 3.00 LPA
Plan monthly/weekly/daily production schedules as per demand & forecasts✔️ Manage inventory of Raw & Packing Materials (RM/PM) + Finished Goods✔️ Coordinate with Production, QA/QC, Engineering & Procurement✔️ Update ERP/MRP systems & generate MIS reports✔️ Ensure compliance with cGMP, GDP & global regulatory standards
🧩 What We’re Looking For✅ Strong knowledge of ...
1 Opening(s)
0 To 1.0 Year(s)
1.00 LPA TO 2.00 LPA
Position: Trainee - Production/Quality
Location: Dabhel - Daman
Experience: 0 - 1 Years
Industries: Pharma
Responsibilities:
Production (Manufacturing) Support:
Assist in batch manufacturing processes such as granulation, compression, coating, filling, and packing under supervision.
Follow Standard Operating Procedures (SOPs) and Batch Manufacturing Records (BMRs).
Ensure cleanroom hygiene, gowning practices, and compliance ...
1 Opening(s)
0 To 1.0 Year(s)
1.00 LPA TO 2.10 LPA
Position: RA Trainee(Khopoli)
Location: Khopoli - Raigarh
Experience: 0 - 1 Years
Industries: Pharma
Responsibilities:
Assist in the preparation and compilation of regulatory dossiers (CTD / ACTD / eCTD) for product registration in various markets.
Support the collection and review of technical documents from R&D, QA, QC, and Production ...
1 Opening(s)
0 To 1.0 Year(s)
2.00 LPA TO 2.10 LPA
Position: QC Trainee
Location: Dabhel - Daman
Experience: 0 - 1 Years
Industries: Pharma
Responsibilities:
Assist in sampling and testing of raw materials, in-process, and finished products as per approved specifications.
Learn and perform routine tests using analytical instruments (e.g., HPLC, UV, IR, pH meter, KF, etc.).
Support the ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: Store Officer
Location: Dabhel - Daman
Experience: 2 - 3 Years
Industries: Pharma
Responsibilities:
Stores & Inventory Management
Receive, inspect, and store raw materials, packing materials, and consumables as per SOPs.
Maintain accurate stock records and perform daily/weekly/monthly stock reconciliations.
Ensure compliance with FEFO (First Expiry First Out) / ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 12.00 LPA
Position: Asst. Manager – External Preparation(P)
Location: Pariya - Vapi
Experience: 10 - 15 Years
Industries: Pharma
Responsibilities:
Production & Compliance:
Oversight of External Preparations, and Oral Liquid Finished Formulations
Ensure adherence to batch manufacturing records (BMR), batch packing records (BPR), and standard operating procedures (SOPs).
Monitor ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
8.00 LPA TO 10.00 LPA
Position: Manager/Sr. Manager - R&D
Location: Vadodara
Experience: 10 - 15 Years
Industries: Pharma
Responsibilities:
Project & Team Management
Lead and manage multiple API development projects across various stages (Route scouting, lab development, scale-up, validation).
Plan and allocate resources effectively among chemists and analysts.
Mentor and guide junior ...
2 Opening(s)
6.0 Year(s) To 10.0 Year(s)
10.00 LPA TO 12.00 LPA
Position: Asst. Manager - R&D
Location: Pariya - Vapi
Experience: 6 - 10 Years
Industries: Pharma
Responsibilities:
Lead formulation development for OSD, external preparations, oral liquids, and injectables.
Oversee pre-formulation studies, prototype development, and scale - up activities.
Ensure compliance with regulatory guidelines (ICH, WHO, USFDA, ...
1 Opening(s)
5.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 12.00 LPA
Position: Executive/Asst. Manager - QC(P)
Location: Vapi
Experience: 5 - 12 Years
Industries: Pharma
Responsibilities:
Analytical Operations:
Perform and supervise analysis of Raw Materials (RM), Packing Materials (PM), and Finished Goods (FG).
Operate and maintain analytical instruments:- HPLC, GC, UV-Vis, FTIR, Dissolution Apparatus
Ensure compliance with ...
10 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 8.00 LPA
Key Responsibilities:
Conduct routine microbiological testing (water, environment, raw materials, in-process & finished products).
Perform environmental monitoring of cleanrooms, utilities, and aseptic areas.
Support media fill, sterility testing, endotoxin testing, and microbial limits testing.
Ensure compliance with cGMP, SOPs, and regulatory guidelines (USFDA, EU, WHO, etc.).
Review and document microbiological data, deviations, and OOS/OOT investigations.
Participate ...