Unichem Laboratories Ltd. is looking for a qualified Production Associates, Validation officer – QA & MEE Officer to join its EHS team & MEE operator at the Pithampur API manufacturing plant.
Walk-in interview details
Date of interview: 21st October – 24 October 2026
Timings: 10.00 AM – 4.00 PM
Venue: Unichem Laboratories Limited 197, Sector 1, Pithampur, Madhya Pradesh – 454775.
We are hiring for following positions
- Production Assocaite API Plant
- MEE Officer EHS Department
- Operator MEE
- Validation officer Quality Assurance API Plant
Production Assocaite API Plant
Department: Production
Role: Associate
Experience: Candidates should have 1-3 years of experience in pharmaceutical API manufacturing, with knowledge of production operations, GMP practices, and safety procedures.
Role & responsibilities
- Carry out API manufacturing activities as per approved Batch Manufacturing Records (BMRs) and Standard Operating Procedures (SOPs).
- Handle and monitor manufacturing equipment such as reactors, centrifuges, filters, dryers, and other process equipment.
- Perform charging, material transfer, filtration, drying, and other unit operations as per process requirements.
- Ensure compliance with cGMP, safety guidelines, and plant procedures.
- Maintain batch records, equipment usage logs, and other production documentation.
- Perform equipment and area cleaning, line clearance, and housekeeping activities.
- Coordinate with Quality Control (QC), Quality Assurance (QA), and Engineering teams for smooth production operations.
- Follow EHS requirements and ensure safe handling of chemicals and raw materials.
Preferred candidate profile
- Experience: 1-3 years in API / pharmaceutical manufacturing.
- Candidates with hands-on experience in API production and chemical process operations will be preferred.
- Willingness to work in shifts.
- Good understanding of safety, discipline, and documentation practices.
- API manufacturing and production operations.
- Knowledge of pharmaceutical cGMP and SOPs.
- Familiarity with reactors, centrifuges, filters, and dryers.
- Batch Manufacturing Record (BMR) documentation.
- Chemical handling and industrial safety practices.
- Equipment cleaning, line clearance, and housekeeping.
- Basic knowledge of process parameters and troubleshooting.
MEE Officer EHS Department
Department: EHS
Role: MEE Officer
Experience: 3 – 6 years
Qualification:
- B.Sc in Chemistry, Environmental Science
- MS/M.Sc(Science) in Chemistry, Environmental science
Role & responsibilities:
- Supervise and monitor Multiple Effect Evaporator (MEE) operations.
- Monitor MEE performance and ensure process parameters remain within specified limits.
- Oversee ETP/STP operations and effluent treatment processes.
- Monitor effluent quality and coordinate sampling and analysis as required.
- Maintain operational records, environmental data, logbooks, and reports.
- Ensure compliance with applicable environmental regulations and site EHS procedures.
- Identify operational issues and coordinate corrective and preventive actions.
- Coordinate with internal teams for environmental monitoring, inspections, and audits.
- Promote safe operating practices and ensure adherence to plant safety procedures.
Preferred candidate profile
- MEE Plant Operations and Monitoring
- ETP/STP Operations
- Effluent Treatment and Management
- Environmental Compliance
- Environmental Monitoring and Documentation
- Process Parameter Monitoring
- Troubleshooting and Root Cause Analysis
- EHS Procedures and Safety Practices
- API Pharmaceutical Manufacturing
Operator MEE
Department: ETP
Role: Operator – MEE
Experience: 3 – 6 years
Qualification: B.Sc. in Chemistry/ Environmental Science
Role & responsibilities
- Operate and monitor Multiple Effect Evaporator (MEE) systems.
- Monitor process parameters such as temperature, pressure, flow rate, and vacuum.
- Operate and monitor ETP/STP systems and associated equipment.
- Monitor effluent treatment processes and ensure smooth plant operations.
- Maintain operational logs, equipment records, and shift reports.
- Identify operational abnormalities and troubleshoot routine equipment issues.
- Follow EHS procedures, safety practices, and environmental compliance requirements.
- Coordinate with the EHS team for routine inspections and maintenance activities.
Required Skills
- Multiple Effect Evaporator (MEE) Operation
- ETP/STP Operations
- Effluent Treatment
- Process Parameter Monitoring
- API Pharmaceutical Industry
- Environmental Safety Practices
- Equipment Troubleshooting
- Operational Documentation
Validation officer Quality Assurance API Plant
Department: Quality Assurance
Role: Validation Officer
Experience: 3 – 5 years
Qualification: B.Sc./ M.Sc.
Role & responsibilities
- Execute and coordinate process validation activities for API manufacturing processes.
- Prepare, review, and execute validation and qualification protocols and reports.
- Perform equipment qualification activities, including IQ, OQ, and PQ.
- Coordinate qualification of utility systems used in API manufacturing.
- Ensure validation activities comply with applicable GMP requirements and approved SOPs.
- Review validation data, identify discrepancies, and support investigations wherever required.
- Coordinate with Production, Engineering, Quality Control, and other relevant departments.
- Ensure proper documentation, traceability, and timely closure of validation activities.
- Support preparation for internal audits and regulatory inspections.
- Maintain validation documentation and records in accordance with site procedures.
Key Requirements:
- 3-5 years of relevant experience in validation/qualification within the pharmaceutical industry.
- API manufacturing plant experience preferred.
- Practical exposure to process validation and equipment/utility qualification.
- Knowledge of GMP requirements and pharmaceutical quality systems.
- Good documentation, analytical, and coordination skills
About Unichem Laboratories
The company Unichem Laboratories Ltd, operates formulation manufacturing facilities at Goa, Ghaziabad (Uttar Pradesh) and Baddi (Himachal Pradesh), and API facilities at Roha and Kolhapur (Maharashtra) and Pithampur (Madhya Pradesh), all approved by USFDA, UK-MHRA, EDQM, TGA, PMDA and other major global health authorities. Supported by a strong R&D centre at Goa focused on NDDS, complex APIs, process chemistry, biotechnology and biosimilars, Unichem caters to diverse therapies including cardiology, neurology, anti-infectives, gastroenterology, musculoskeletal and dermatology.