Associate
Lupin · Greater Aurangabad Area
- Experience2–5 yrs
- SalaryNot disclosed
- Work modeonsite
- Levelmid
- Posted18 Sept 2026
About Lupin
Lupin is hiring in Greater Aurangabad Area in pharma biotech. This role looks for around 2+ years of experience.
Skills
- cGMP
- GxP
- Good Manufacturing Practice
- Standard Operating Procedures
- Batch Manufacturing Records
- granulation
- compression
- coating
- encapsulation
- in-process checks
- equipment calibration
- preventive maintenance
The role
A production associate at a pharmaceutical manufacturing company operates granulation, compression and coating processes, applying cGMP and Good Manufacturing Practice to batch manufacturing and in-process checks. The role also uses Standard Operating Procedures and Batch Manufacturing Records to maintain compliant production.
Full job description
Job Description
Department: Production
Designation: Associate- Production
Working Section: Granulation, Compression, Coating and Encapsulation
Comply with all cGMP, GxP and any other applicable regulatory requirement, including EH&S requirements.
Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task.
Conduct all tasks/activities as per the applicable SOPs. Report any difficulty or deviation in following the procedure/instruction to immediate supervisor/managers.
Report any quality concern or suggestion for improvement to supervisors/ managers.
Manufacturing / processing of batches of assigned products under supervision as per instructions given in the BMR.
Handling and movement of raw material, bulk, semi-finished and finished goods.
Operation, washing and cleaning of equipment’s and accessories used in related production activities as per respective SOP.
Up-keeping area and machines as per GMP requirements.
To Support Quality Management Systems and to report any discrepancy, abnormity, non-conformance or any incidence observed to the Department Head and QA Head.
Receipt of RM and PM from Warehouse and ensuring overall cleanliness of areas.
Doing operations as per the SOPs and BMR with online recording in respective documents as applicable.
To ensure self-hygiene before entering in the production area and follow all the other rules & regulation set by HR department.
Performing in-process checks as per respective BMR and recording of results of in respective documents as applicable.
To fulfil the training need as per current needs with respect to cGMP, Job, safety, health & Hygiene by attending the training programmes.
Cost effectiveness in production operation by controlling overtime, revenue expenses and achieving standard yield.
Critically monitoring of the environmental conditions with a view to meet the standards mentioned in BMR and SOP.
Ensure calibration and preventive maintenance of manufacturing equipment and instruments as per approved schedule and the results of same meeting the standards.
To perform line clearance activity during batch to batch and product to product change over and ensure the compliance as per SOP.
Issuance, retrieval and destruction of dies and punches, product dedicated bags and sieves, silicon sleeves, pipes, hose pipes and screens.
To ensure the audit compliance.
Trouble-shooting: To attend the problems of machine and process as and when necessary.
Any other assignment allocated by production Head.
To attend required cGMP/ On Job /Functional training activities as per planner.
Work Experience
2 to 5 years.
Education
Diploma
Competencies
Innovation & Creativity
Result Orientation
Collaboration
Customer Centricity
Developing Talent
Stakeholder Management
Strategic Agility
Process Excellence