Teva Supv Production - TAPI 

India, Uttar Pradesh 

3317041

• 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

M.Sc. : Minimum Experience 9 year in Pharma

B.Tech / B.E (Chemical) : Minimum Experience 5 to 7 years

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