Production Manager
1 Nos.
114643
Full Time
12.0 Year(s) To 15.0 Year(s)
13.00 LPA TO 15.00 LPA
Production / Quality / Maintenance
Pharma/Biotech/Clinical Research
B.Tech/B.E. - Chemical; M.Sc / MS Science - Chemistry
Job Description:
Position: Production Manager
Location: Vapi
Experience: 12 - 15 Years
Industries: Pharma
Responsibilities:
- Overall responsible for planning and maintenance of optimum inventory of raw materials, in – process and finished goods.
- To ensure the products are manufactured and stored according to pre-approved instructions to obtain required quality.
- Implementation of procedures related to intermediates or APIs manufacturing processing production areas.
- Regular review & evaluation of production record for- quality and yields and completeness prior to submission in Quality Assurance.
- To ensure required initial and continuing training for department personal shall carried out according to need.
- To review of master formula record, Batch Manufacturing record and Standard Operating Procedure.
- To ensure activity shall be done by qualified personnel & recorded online at the time they performed.
- Making sure that production deviations are reported and evaluated and that critical deviations are investigated and the conclusions are recorded.
- Evaluating proposed changes in product, process or equipment.
- Ensure that no Impact on product quality, safety & productivity for proposed changes.
- New or modified Facilities and equipment's are qualified prior to use.
- 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.
- Making sure that production facilities are clean and appropriately disinfected.
- To sanction leave to the staff in consultation with Works Executive to Meets production targets & planning resources.
- Ensure optimum operation and utilization of plant and machine for timely production of finished products as per dispatch plan.
- Impart training to employee on production operation, SOPs & proposed changes related to implementation of CAPA.
- To effectively handle & explain the regulatory/customer investigator during the audit/inspection.
- Planning of manpower/ resource to meets the production targets & timely dispatch of material.
- PPS section QAMS, DMS activities to be performed in absence of respective person.
- Handling of manufacturing investigation as part of OOS / OOT / Market complaints / rejected or recalls material etc.
- Involving in the investigation and review / approval of Incident, Change controls, CAPA, SOPs MFR, BMR etc. in QAMS/DMS application.
Required Skills:
- Must be excellent in written and spoken English; net savvy and adept at computer skills.
- Logical thinking.
- Organizing.
- Good in communication.
Required Qualification: - M.Sc/B.E/B.Tech - Chemical
Salary :- Upto 15.00 LPA
If you are interested in this opening, please send updated resume on same mail with following details.
Total No. of Years Experience: -
Current CTC: -
Expected CTC: -
Notice Period: -
Key Skills :
Company Profile
Leading API Manufacturing USFDA Approved Company located at Vapi
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