Supv Production - TAPI
Gajraula, India, 244235
Who we are
TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service.
Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market.
How you’ll spend your day
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Responsible for implementing the instruction and producing APIs or intermediates as per approve instruction.
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Responsible for proper storage of raw materials, dispensing and storage of Intermediate and finished goods in designated areas and labeling as per applicable procedures.
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Maintaining documents and batch cards as per approved instruction and issuing documents relating the facility’s activities for ensuring implementation.
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To achieve production targets as per plan.
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To coordinate with safety, Maintenance and QA/QC for shift activities.
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To ensure maintenance & cleanliness of critical utilities (if applicable) as per procedures.
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Carrying out batch processing including raw material charging, unloading of material and sampling activities during intermediate production.
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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
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Act as qualified trainer of those with less experience. Conduct in-direct supervision of others in the team
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Provides input into annual performance evaluations of production technicians as applicable. Investigate and resolve problems. Clear and concise communication to Process Lead and Supervision
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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.
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As an Opex champion, identification of improvements projects in respective area and supporting functional head to implement the project
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Extensive Knowledge of Documentation in the Pharmaceutical industry related to process & cleaning validation, DHT, CHT , Cleaning Verification etc.
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Extensive Knowledge to carried out investigation of any OOS/OOT/ Deviation with proper tools.
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Preparation of batch card, qualification protocol, report & other GMP related documents.
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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
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