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.10.Ensure that no Impact on product quality, safety & productivity for proposed changes.
11.New or modified Facilities and equipment's are qualified prior to use.
12.To develop reprocess/ rework procedure for non-conformance of Intermediate and APIs & report to all production related activities/ issues to General Manager (Plant Head)/Director.
13.Making sure that production facilities are clean and appropriately disinfected.
14.To sanction leave to the staff in consultation with Works Executive to Meets production targets & planning resources.
15.Ensure optimum operation and utilization of plant and machine for timely production of finished products as per dispatch plan.
16.Impart training to employee on production operation, SOPs & proposed changes related to implementation of CAPA.
17.To effectively handle & explain the regulatory/customer investigator during the audit/inspection.
18.Planning of manpower/ resource to meets the production targets & timely dispatch of material.
19.PPS 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 etc. in QAMS/DMS application.
experience
12show more 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.10.Ensure that no Impact on product quality, safety & productivity for proposed changes.
11.New or modified Facilities and equipment's are qualified prior to use.
...
12.To develop reprocess/ rework procedure for non-conformance of Intermediate and APIs & report to all production related activities/ issues to General Manager (Plant Head)/Director.
13.Making sure that production facilities are clean and appropriately disinfected.
14.To sanction leave to the staff in consultation with Works Executive to Meets production targets & planning resources.
15.Ensure optimum operation and utilization of plant and machine for timely production of finished products as per dispatch plan.
16.Impart training to employee on production operation, SOPs & proposed changes related to implementation of CAPA.
17.To effectively handle & explain the regulatory/customer investigator during the audit/inspection.
18.Planning of manpower/ resource to meets the production targets & timely dispatch of material.
19.PPS 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 etc. in QAMS/DMS application.
experience
12show more
