1 Opening(s)
7.0 Year(s) To 12.0 Year(s)
7.00 LPA TO 10.00 LPA
Position: Executive/Sr. Executive - Production
Location: Daman
Experience: 7 - 12 Years
Industries: Pharma Formulation
Responsibilities:
Manage day-to-day production operations, ensuring timely and efficient manufacturing.
Ensure compliance with GMP, safety, and environmental regulations.
Optimize production processes to improve efficiency, reduce costs, and maintain product quality.
Monitor and control production schedules, ...
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)
5.0 Year(s) To 6.0 Year(s)
6.00 LPA TO 7.00 LPA
Position: RA Executive (Khopoli)
Location: Khopoli - Raigarh
Experience: 5 - 6 Years
Industries: Pharma
Responsibilities:
Dossier Preparation & Submission
Prepare, compile, and review CTD / ACTD / eCTD dossiers for product registration in global markets.
Coordinate for ANDA, DMF, CEP, COS, and other regulatory submissions for APIs and ...
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)
15.0 Year(s) To 20.0 Year(s)
15.00 LPA TO 20.00 LPA
Position: Factory Manager
Location: Bhimpore - Daman
Experience: 15 - 20 Years
Industries: Pharma
Responsibilities:
Regulatory Compliance: Ensure adherence to global regulatory standards including USFDA, MHRA, WHO, and GMP.
cGMP & Quality: Implement and monitor current Good Manufacturing Practices across all manufacturing and packaging operations.
Plant Operations Management: ...
2 Opening(s)
1.0 Year(s) To 2.0 Year(s)
3.00 LPA TO 3.75 LPA
Position: Production Supervisor
Location: Silvassa
Experience: 1 - 2 Years
Industries: Chemical
Responsibilities:
Supervise and monitor day-to-day production activities on the shop floor.
Ensure production targets are achieved within defined timelines.
Maintain quality standards and ensure compliance with SOPs and GMP.
Implement and monitor safety procedures as per company policy.
Plan manpower allocation and ...
2 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.50 LPA TO 4.00 LPA
Position: QA Officer
Location: Vapi
Experience: 2 - 5 Years
Industries: Pharma
Responsibilities:
Documentation & Record Review:
Review specifications, sampling instructions, test methods, and analytical reports.
Review and approval of Batch Manufacturing Record (BMR), Batch Packing Record (BPR), Master Formula Record (MFR), and Equipment Qualification Records.
Review completed Batch ...
2 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 6.00 LPA
Key Responsibilities:
Preventive, predictive & breakdown maintenance of plant & utility equipment (Water, Steam, HVAC, Pneumatic, Hydraulic).
Ensure compliance with cGMP, cGLP, GDP, GEP & safety policies.
Manage validation, qualification, calibration & engineering documentation.
Plan and execute preventive maintenance programs to minimize downtime.
Coordinate with production & external agencies for timely maintenance.
Oversee pest control, site ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
Not Disclosed by Recruiter
Documentation & Compliance
Prepare, review, control BMRs, SOPs, logbooks, and formats.
Ensure cGMP & ALCOA+ compliance in documentation.
Manage DocuSign workflows, approvals, revisions, and closures.
Maintain archives for audits/inspections.
Production Support
Record and verify production data in SAP/digital systems.
Coordinate with QA/QC/Engineering/Stores for timely closures.
Review PISCADA reports with batch documentation.
Support OQ/PQ documentation for equipment/utilities.
QMS & Regulatory
Manage QMS ...
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 ...