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50 Watson Pharmaceuticals Jobs
Supv Production - TAPI
Watson Pharmaceuticals
posted 2d ago
Job Role Insights
Fixed timing
Key skills for the job
Job Description
Responsible for implementing the instruction and producing APIs or intermediates as per approve instruction.
Responsible for proper storage of raw materials, dispensing and storage of Intermediate and finished goods in designated areas and labeling as per applicable procedures.
Maintaining documents and batch cards as per approved instruction and issuing documents relating the facility s activities for ensuring implementation.
To achieve production targets as per plan.
To coordinate with safety, Maintenance and QA/QC for shift activities.
To ensure maintenance cleanliness of critical utilities (if applicable) as per procedures.
Carrying out batch processing including raw material charging, unloading of material and sampling activities during intermediate production.
Qualified in Production Tech and Senior Production Technician duties: Assigning daily tasks to production technicians pertaining to manufacturing of encapsulated products, while completing manufacturing documentation per approved procedures. Includes reviewing documentation for completeness and accuracy per established timelines
Act as qualified trainer of those with less experience. Conduct in-direct supervision of others in the team
Provides input into annual performance evaluations of production technicians as applicable. Investigate and resolve problems. Clear and concise communication to Process Lead and Supervision
Extensive equipment knowledge to perform trouble shooting and root cause analysis. Develops solutions to complex problems requiring resourcefulness and creativity/innovation and ensures solutions are consistent with organization s objectives.
As an Opex champion, identification of improvements projects in respective area and supporting functional head to implement the project
Extensive Knowledge of Documentation in the Pharmaceutical industry related to process cleaning validation, DHT, CHT , Cleaning Verification etc.
Extensive Knowledge to carried out investigation of any OOS/OOT/ Deviation with proper tools.
Preparation of batch card, qualification protocol, report other GMP related documents.
Working experience and knowledge about the Liquide chromatography Spray drying
Your experience and qualifications
M.Sc. : Minimum Experience 9 year in Pharma
B.Tech / B.E (Chemical) : Minimum Experience 5 to 7 years
Employment Type: Full Time, Permanent
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based on 27 employees
Strict timing
Monday to Friday
No travel
Day Shift
Watson Pharmaceuticals Benefits
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