Promoted by the late Mr. Amrut Mody, a pioneer of the Indian pharmaceuticals business, Unichem Laboratories has grown to become one of India’s most respected pharmaceutical companies. It is committed to deliver better health through superior products. By combining strategic research and in-depth industry knowledge, Unichem aims to transform itself into a global pharmaceutical drug Company with an increasing focus on cutting-edge research and developed markets.
- Vacancy details:
- Department: Sr. Officer/Officer Production API
- Qualification:Diploma in Chemical, B.Sc in Chemistry, MS/M.Sc(Science) in Chemistry
- Experienced: 5 – 7 years
- Salary: ₹4.5-6.5 Lacs P.A.
Job Description: Greetings from Unichem Laboratories Ltd .!!
Important Details :
- Location:Pithampur
- Post of date:17/08/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To Face Interview
- Interview Rounds of Interview: HR
Walkin Interview Details:
Date:21st August – 24 August
Time:10.00 AM – 4.00 PM
Venue: Unichem Laboratories Limited, Plot No. 197 Sector 1, Pithampur, Madhya Pradesh
Job description
Role & responsibilities:
1. To ensure that all the SOPs, cGMP practices & safety guidelines in the company.
2. To achieve at par or above monthly budgeted production with consistent quality & yield with zero accidents.
3. Batch Production Record Issuance & production planning.
4. Attending the necessary trainings provided by the company & maintain training records, training planner, etc.
5. Giving hot & cold work permits, maintenance work permits related to the working area.
6. Prepare & maintain Organogram, shift schedule, daily & monthly report.
7. Overall product quality review on daily basis.
8. Prepare & maintain the intermediate finished stock & recovered solvent records of all products.
9. Keeping and maintaining the documents related to plant in presentable from (For external and internal audits)
10. Preparing & updating SOPs, BPRs, etc. as applicable.
11. Carrying out investigation for deviations, OOS, market complaints & submitting the necessary reports.
12. Preparation of compliance report to QA against Out of specification test results, market complaints & internal/external Audits.
13. Update the job responsibilities of officers, Jr. supervisors & their allocation.
14. Conduct self-inspection in plant to meet cGMP & FDA requirements
