Production Associate/ Pharma industry

Avani Consulting; Mysuru; On-site; INR 400,000 - 700,000; Full time

Job summary

Avani Consulting in Mysore invites applications for Production Associate in a leading pharmaceutical API manufacturing setup. The role focuses on planning and executing production batches while adhering to cGMP and safety standards.

The ideal candidate has 3–8 years of API manufacturing experience, with a BE/B.Tech/M.Tech in Chemical Engineering or MSc in Chemistry, and will work on-site in Mysore.

Qualifications

• BE/B.Tech/M.Tech in Chemical Engineering.
• MSc in Chemistry.

Responsibilities

• Plan and execute batches per commitments, ensuring cGMP and safety.
• Maintain gowning, entry/exit, PPE usage.
• Follow Batch Manufacturing Records and SOPs.
• Maintain good housekeeping on the shop floor.
• Ensure cGMP, safety, health and environment compliance.
• Review batch records before QA release.
• Report deviations and coordinate investigations with cross-functional teams.
• Ensure online documentation with signatures and dates.
• Monitor manufacturing environment and daily logs.
• Oversee preventive maintenance and calibration schedules.
• Perform department sanitization activities.
• Assist QA in investigations related to OOS, deviations, CAPA.
• Label raw material/intermediates/APIs at each stage with proper storage.
• Reconcile stocks at regular intervals.
• Take on any other assignment from Production head.

Education

BE/B.Tech/M.Tech in Chemical Engineering

MSc in Chemistry

Job description

Production Associate

We are hiring for the position of Production Associate with a leading Pharmaceutical API Manufacturing Industry.

Position: Associate

Interview Mode: Face - to - Face (At Mysore)

Hiring Date: 31-10-2026

Work Experience: 3 - 8 years in API Manufacturing

CTC: 4 - 7 LPA

Location: Mysore

Gender: Male

Qualifications

• 1.B.E./B.Tech/M.Tech in Chemical Engineering
• 2.MSc in Chemistry

Roles & Responsibilities

• 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements.
• 2. To ensure gowning practices, entry / exit procedures, usage of PPEs are followed by team while in the department.
• 3. To ensure adherence of process instructions as per Batch Manufacturing Record and respective departmental procedures.
• 4. To ensure good housekeeping in the production shop floor.
• 5. To ensure compliance to cGMP, Safety, Health & Environment in delivering the product of intended Quality.
• 6. To ensure batch records on completion are reviewed for adequacy prior to hand over to QA for review, compliance & release / rejection.
• 7. To report deviations / incidents immediately upon occurrence and to conduct investigation in coordination with cross-functional teams.
• 8. To ensure all document entries are performed online with legible, errors corrected with signature and date.
• 9. Monitoring and control of manufacturing environment and filling of daily log books.
• 10. To ensure preventive maintenance of equipment, calibrations of gauges / instruments are performed as per schedule & the outcome of verification is within control.
• 11. To ensure the sanitization activity is performed in the department.
• 12. To support QA in investigations related to OOS, Deviations, CAPA, Incidents, complaints or recalls, validations and any other support that would be required.
• 13. To ensure the raw material / Intermediates / API(s) are labelled at each stage of process and stored with appropriate segregation at recommended storage conditions ensuring no impact on product Quality.
• 14. To ensure that stocks are reconciled at regular intervals.
• 15. Any other assignment allocated by Production head.