Production Manager

Production Manager

1 Nos.
119472
Full Time
8.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
Production / Quality / Maintenance
Pharma/Biotech/Clinical Research
B.Tech/B.E. - Chemical
Job Description:

Position:          Production Manager

Location:         Vapi

Experience:      12 - 15 Years

Industries:       Pharma - API

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

  • Excellent communication skill, with computer proficiency.
  • Very good in negotiation, coordination, organization, and problem solving skill.
  • Ability to multitask, time management, work in a fast-paced environment, and should able to meet deadlines.

 

Required Qualification: - M.Sc/B.E/B.Tech - Chemical

Salary :- Upto 15.00 LPA

If you are interested for this opening please send updated resume on same mail with following details.

 

Total No. of Years Experience :-

Current CTC :-

Expected CTC :-

Notice Period :-

Company Profile

It is a leading Pharma API & Formulation Industry

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