Manager Production
Manager Production
Posted on :
21-08-2025
Employer Active
1 Vacancy
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Share
Send me jobs like this
Job Alert
You will be updated with latest job alerts via emailValid email field required
Send jobs
Job Description
1. Overall responsible for planning and maintenance of optimum inventory of raw materials in process and finished goods.
2. To ensure the products are manufactured and stored according to pre-approved instructions to obtain required quality.
3. Implementation of procedures related to intermediates or APIs manufacturing processing production areas.
4. Regular review & evaluation of production record for- quality and yields and completeness prior to submission in Quality Assurance.
5. To ensure required initial and continuing training for department personal shall carried out according to need.
6. To review of master formula record Batch Manufacturing record and Standard Operating Procedure.
7. To ensure activity shall be done by qualified personnel & recorded online at the time they performed.
8. Making sure that production deviations are reported and evaluated and that critical deviations are investigated and the conclusions are recorded.
9. Evaluating proposed changes in product process or equipment.
2. To ensure the products are manufactured and stored according to pre-approved instructions to obtain required quality.
3. Implementation of procedures related to intermediates or APIs manufacturing processing production areas.
4. Regular review & evaluation of production record for- quality and yields and completeness prior to submission in Quality Assurance.
5. To ensure required initial and continuing training for department personal shall carried out according to need.
6. To review of master formula record Batch Manufacturing record and Standard Operating Procedure.
7. To ensure activity shall be done by qualified personnel & recorded online at the time they performed.
8. Making sure that production deviations are reported and evaluated and that critical deviations are investigated and the conclusions are recorded.
9. Evaluating proposed changes in product process or equipment.
that no Impact on product quality safety & productivity for proposed changes.
or modified Facilities and equipments are qualified prior to use.
develop reprocess/ rework procedure for non-conformance of Intermediate and APIs & report to all production related activities/ issues to General Manager (Plant Head)/Director.
sure that production facilities are clean and appropriately disinfected.
sanction leave to the staff in consultation with Works Executive to Meets production targets & planning resources.
optimum operation and utilization of plant and machine for timely production of finished products as per dispatch plan.
training to employee on production operation SOPs & proposed changes related to implementation of CAPA.
effectively handle & explain the regulatory/customer investigator during the audit/inspection.
of manpower/ resource to meets the production targets & timely dispatch of material.
section QAMS DMS activities to be performed in absence of respective person
20. Handling of manufacturing investigation as part of OOS / OOT / Market complaints / rejected or recalls material etc.
21. Involving in the investigation and review / approval of Incident Change controls CAPA SOPs MFR BMR QAMS/DMS application.
or modified Facilities and equipments are qualified prior to use.
develop reprocess/ rework procedure for non-conformance of Intermediate and APIs & report to all production related activities/ issues to General Manager (Plant Head)/Director.
sure that production facilities are clean and appropriately disinfected.
sanction leave to the staff in consultation with Works Executive to Meets production targets & planning resources.
optimum operation and utilization of plant and machine for timely production of finished products as per dispatch plan.
training to employee on production operation SOPs & proposed changes related to implementation of CAPA.
effectively handle & explain the regulatory/customer investigator during the audit/inspection.
of manpower/ resource to meets the production targets & timely dispatch of material.
section QAMS DMS activities to be performed in absence of respective person
20. Handling of manufacturing investigation as part of OOS / OOT / Market complaints / rejected or recalls material etc.
21. Involving in the investigation and review / approval of Incident Change controls CAPA SOPs MFR BMR QAMS/DMS application.
Employment Type
Full-time
Key Skills
Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.
