5 Opening(s)
3.0 Year(s) To 5.0 Year(s)
0.50 LPA TO 6.00 LPA
Job Summary: We are looking for a highly motivated and detail-oriented R&D Research Associate to join our API development team. The ideal candidate will be responsible for supporting the design, development, and optimization of synthetic processes for Active Pharmaceutical Ingredients (APIs), ensuring scalability, regulatory compliance, and quality standards. This role ...
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)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 3.60 LPA
Roles & Responsibilities:
Oversee operation and maintenance of electrical systems including transformers, VCB, ACB, LT/HT panels, and motors.
Perform preventive, predictive, and breakdown maintenance for all electrical equipment.
Ensure smooth and uninterrupted power supply to all plant departments and utilities.
Lead troubleshooting and root cause analysis (RCA) of electrical faults and implement corrective actions.
Maintain ...
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 ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 5.00 LPA
Position: QA Officer
Location: Vapi
Experience: 2 - 5 Years
Industries: Pharma API
Responsibilities:
To impart the departmental training & co-ordinate for cGMP training as per planned schedule.
To Coordination of Regulatory/Customer audit and its compliance. Review the audit feedback and provide the action ...
2 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: Research Associate
Location: Vadodara
Experience: 3 - 5 Years
Industries: Pharma
Responsibilities:
Synthetic Chemistry / Lab Work
Perform multi-step organic synthesis of target molecules as per project requirements.
Conduct reaction monitoring, work-up, purification, and isolation of intermediates and final products.
Maintain accurate lab records and notebooks (ELN ...
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 ...
9 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 3.60 LPA
Job Description: Production Executive
We are looking for a Production Executive with hands-on experience in API manufacturing to join our dynamic production team. The ideal candidate will be responsible for supervising daily production activities, ensuring batch operations run smoothly, and maintaining compliance with safety and quality standards.
Key Responsibilities:
Execute and monitor day-to-day ...
10 Opening(s)
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 7.00 LPA
Industry: Pharma Formulation
Openings: 10Experience: 3–7 YearsPreference: Male Candidates only / Gujarati-speaking
Key Responsibilities:
Perform testing of Raw Materials (RM) & Packaging Materials (PM) as per pharmacopoeial standards.
Ensure timely release of materials with accurate documentation.
Follow cGMP, GLP, and regulatory compliance in QC lab.
Maintain records, calibration logs, and SOP adherence.
Coordinate with QA, Production, and Warehouse for smooth operations.
Requirements:
B.Sc./M.Sc. ...