2 Opening(s)
1.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 8.00 LPA
Key Responsibilities:
1 Responsible for aseptic inoculum preparation, transfer, sampling and sterility. Timely release of fermentation inoculum.
2 Perform periodic monitoring of facility (Settle plate, Swabs, Samplings, etc)3 Timely analysis, reporting to the Shift In charge during Production.4 Logical expression of plates, reporting and support to Production.5 Ensure that Culture is properly ...
1 Opening(s)
2.0 Year(s) To 7.0 Year(s)
2.00 LPA TO 5.00 LPA
Job Title:
Warehouse Operator – Dispensing (Formulation Plant)
Department:
Warehouse / Stores – Dispensing Section (Formulations) 📍 Location: [Insert Location] 🕒 Experience: 2 to 5 Years 🎓 Qualification: B.Pharm / M.Pharm / Diploma in Pharmacy (Mandatory)
Job Summary:
We are hiring a dedicated Warehouse Operator – Dispensing for our Formulation manufacturing facility, responsible for precise ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
Not Disclosed by Recruiter
Job Description:
We are looking for an IPQA Executive to monitor and ensure in-process quality during manufacturing and packing operations in our API facility. The ideal candidate will be responsible for real-time quality assurance, GMP compliance, and documentation control throughout the production lifecycle.
Key Responsibilities:
Perform in-process checks during various stages of API ...
2 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 6.00 LPA
Execute preventive and breakdown maintenance of all equipment's (Plant & Utility) as per respective equipment checklist and SOP.
Predictive Maintenance to Reduce Down Time
Ensuring that all activities are performed in accordance with cGMP, cGLP, Company SOP and health & safety policies at site.
Validation and Qualification of Equipment and Facilities.
Management of the ...
2 Opening(s)
1.0 Year(s) To 3.0 Year(s)
1.50 LPA TO 5.00 LPA
Key Responsibilities:
1. Recruitment & Staffing
Handle recruitment for manufacturing, QA, QC, production, engineering, warehouse, and admin departments.
Screen resumes, schedule interviews, conduct HR rounds, and manage offer letters.
Coordinate with department heads for manpower planning.
2. Onboarding & Induction
Complete joining formalities, new employee documentation, ID cards, and induction program.
Ensure training on GMP, safety, and ...
1 Opening(s)
7.0 Year(s) To 10.0 Year(s)
Not Disclosed by Recruiter
Automation & Control System Management-
Lead the operation, maintenance, configuration, and troubleshooting of Programmable Logic Controllers (PLC), Supervisory Control and Data Acquisition (SCADA) systems, and Distributed Control Systems (DCS).
Ensure high availability and reliability of all critical automation and control systems across the facility.
Manage system backups, security, and lifecycle management for all ...
1 Opening(s)
6.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 7.50 LPA
Key Responsibilities:•Handling of QMS tools like change control, CAPA, Deviation etc.•Handle QA efficiently and able to maintain documentation as per GMP.•Preparation and maintenance of training schedule and co-ordinate with working staff to establish Procedures, Standards and System.•Preparation of Raw Material and Finished Product specification in accordance with Regulatory Guideline.•Vendor Evaluation, ...
2 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 6.00 LPA
Execute preventive and breakdown maintenance of all equipment's (Plant & Utility) as per respective equipment checklist and SOP.
Predictive Maintenance to Reduce Down Time
Ensuring that all activities are performed in accordance with cGMP, cGLP, Company SOP and health & safety policies at site.
Validation and Qualification of Equipment and Facilities.
Management of the ...
3 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 3.60 LPA
Roles & Responsibilities:
Operate and maintain utility equipment like chillers, air compressors, and nitrogen plants.
Perform routine checks, preventive maintenance, and troubleshooting of utility systems.
Ensure uninterrupted supply of utilities (air, water, nitrogen, cooling, etc.) to production areas.
Maintain daily utility logs, pressure/temperature records, and compliance checklists.
Follow cGMP, safety standards, and SOPs during utility ...
2 Opening(s)
3.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 6.00 LPA
Position: QC Manager Location: Palanpur, Gujarat Industry: Pharma – API
Key Responsibilities:
Lead and oversee Quality Control operations in compliance with cGMP & regulatory guidelines.
Manage QC documentation, including qc document review, SOPs, and analytical records.
Supervise laboratory activities such as RM, PM, in-process, and finished product testing.
Ensure timely calibration, qualification, and maintenance of ...