1 Opening(s)
2.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 6.00 LPA
Perform routine quality control analysis of raw materials, packing materials, in-process and finished products.
Operate and maintain HPLC and GC instruments for analytical testing.
Perform sample preparation, testing and documentation as per approved SOPs and specifications.
Review analytical results and ensure compliance with specifications.
Maintain proper laboratory records, logbooks and analytical worksheets.
Follow GMP, GLP ...
2 Opening(s)
2.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 4.00 LPA
Key Responsibilities
Manage receipt, storage, and issue of raw materials, packing materials, and finished goods.
Ensure proper identification, labeling, segregation, and storage of materials as per GMP guidelines.
Maintain warehouse records, stock registers, and inventory documentation.
Handle material inward/outward activities and coordinate with Production, QC, and QA departments.
Follow FIFO/FEFO practices and ensure proper stock ...
10 Opening(s)
1.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 6.00 LPA
Machines / Equipment
Candidates with hands-on experience in any of the following machines:
Vial Filling & Sealing Machine
Ampoule Filling & Sealing Machine
Pre-filled Syringe Filling Machine
Vial Washing Machine
Key Responsibilities
Operate aseptic area machines as per SOP, BMR and GMP requirements.
Perform machine setup, operation, changeover and cleaning.
Monitor machine parameters, filling accuracy, speed and output.
Handle loading/unloading ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
Key Responsibilities
Handling of bulk chemical storage tanks and transfer operations
Loading & unloading of raw materials, solvents, and finished products
Monitoring tank levels, temperature, pressure, and flow parameters
Safe operation of pumps, valves, pipelines, and transfer systems
Maintaining proper records of tank farm activities and material movements
Coordination with production, utility, and EHS departments
Ensuring compliance ...
3 Opening(s)
1.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 6.00 LPA
Job Responsibilities (Universal Chemicals)
Ensure all products meet quality standards and specifications.
Perform in-process and final product quality checks.
Review and maintain QA documents, records, and reports.
Prepare and update SOPs, specifications, and quality documents.
Monitor GMP, safety, and quality compliance in the plant.
Handle deviations, CAPA, and change control activities.
Participate in internal and external quality ...
1 Opening(s)
4.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 5.00 LPA
Key Responsibilities
Perform analysis of raw materials, in-process samples, finished products, and stability samples.
Operate and maintain laboratory instruments such as HPLC, GC, UV, FTIR, and other analytical equipment.
Prepare, review, and maintain QC documentation, test reports, and laboratory records.
Follow Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and data integrity requirements.
Ensure compliance ...
2 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
Responsible for taking ownership for safety and quality related compliance execution in respective work areas as per defined company standards.
Responsible for maintaining shift wise logbooks as per defined standard /operating procedure/ work instructions.
Responsible for maintaining excellent 5S /housekeeping standards in respective work area.
Responsible for reporting any deviation / abnormalities to ...
1 Opening(s)
0 To 3.0 Year(s)
3.00 LPA TO 4.00 LPA
JD for Process Engineer: -Location: Jhagadia PlantDepartment: Process EngineeringExperience: 2-5 YearsQualification: B.E./B. Tech in Chemical Engineering.Budget: 7 LPA
Job SummaryWe are seeking a dynamic and result-oriented Process Chemical Engineer with 2-5 years of industrialexperience to support process optimization, scale-up activities, troubleshooting, and continuousimprovement initiatives. The candidate will work closely with Production, ...
3 Opening(s)
1.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 6.00 LPA
Job Responsibilities (Universal Chemicals)
Ensure all products meet quality standards and specifications.
Perform in-process and final product quality checks.
Review and maintain QA documents, records, and reports.
Prepare and update SOPs, specifications, and quality documents.
Monitor GMP, safety, and quality compliance in the plant.
Handle deviations, CAPA, and change control activities.
Participate in internal and external quality ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 5.00 LPA
🏭 Asence Pharma Pvt. Ltd. is looking for a proactive and experienced HR Officer to join our team at our API Manufacturing Facility in Ranoli, Vadodara.
📍 Location: Ranoli, Vadodara, Gujarat 🏢 Industry: API / Pharmaceutical Manufacturing 💼 Experience: 2–4 Years 🎓 Qualification: MBA (HR) / MSW / MHRM
✅ Mandatory Requirements
Experience ...