Title Not mentioned in the provided Description. Zydus Group

2.0 - 10.0 years

0 Lacs

ahmedabad, gujarat

On-site

**Role Overview:** If you have the talent and zeal, an opportunity awaits you to join our Greenfield Injectable manufacturing plant at Ahmedabad in various roles such as Production, Engineering, Quality Assurance, and Quality Control. **Key Responsibilities:** - **Production: Shift In charge** - Supervising Injectable production with a B. Pharm/M.Pharm qualification and 3 to 10 years of experience. - **Production: Operator/Tech. Associate** - Operating in Injectable production with an I.T.I./ Diploma qualification and 2 to 8 years of experience. - **Engineering: Shift Incharge** - Handling Instrumentation, Plant maintenance, Engineering QMS for Injectable Manufacturing Plant with a B.E./B.Te...

Posted 5 days ago

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Engineering QMS - Lead - Unison Pharmaceuticals Unison Pharmaceuticals

10.0 - 15.0 years

8 - 18 Lacs

ahmedabad

Work from Office

Unison Pharmaceuticals is seeking candidates for the role of Engineering QMS - Lead for our EU Approved Facility, Unit III Company : Unison Pharmaceuticals Ltd. Location : Moraiya, Ahmedabad - Unit III Designation : Upto Manager Job Role/Position: Engineering QMS - Lead Experience Required : 1015 Years (Pharma Industry OSD preferred) Key Responsibilities Preparation, review, and implementation of SOPs in line with GMP compliance . Review and control of daily operation logbooks and engineering documentation . Operation & Maintenance knowledge of utility equipment, HVAC, and water systems . Handling breakdown maintenance of utility and process equipment. Initiation, handling, and documentation...

Posted 1 month ago

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Executive - Engineering Documentation (API Unit) @Bhiknoor, Kamareddy MSN Group

2.0 - 5.0 years

3 - 5 Lacs

Bhiknoor

Work from Office

Job Summary: We are seeking a detail-oriented and process-driven Executive Engineering Documentation to manage and maintain engineering records and documentation related to equipment qualification, change control, and plant utilities. The ideal candidate should be well-versed with GMP documentation practices , engineering schedules , and technical drawing updates . Key Responsibilities: Prepare, review, and maintain equipment qualification documents (IQ/OQ/PQ). Assist in managing Change Control procedures related to equipment and utility modifications. Prepare and update logbooks, calibration schedules, preventive maintenance schedules , and related engineering records. Verify and maintain d...

Posted 3 months ago

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