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Operator III - TAPI Job Details | Teva Pharmaceuticals

2.00 to 5.00 Years Gwalior (Madhya Pradesh) 18 May, 2025

Job Location	Gwalior (Madhya Pradesh)
Education	M.Sc. (Science)B.Sc. (Science)
Salary	As per Industry Standards
Industry	Telecom, IT-Hardware/Networking
Functional Area	Production/Manufacturing/Maintenance/Packaging
EmploymentType	Full-time

Job Description

Operator III - TAPIDate: Apr 30, 2025Location: Gwalior, India, 477117Company: Teva PharmaceuticalsJob Id: 61727Who we areTAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industrys broadest portfolio including over 350 API products, we are the go-to global supplier for APIs, supporting 80 PERCENT 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 enables 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 headquarters 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 youll spend your day

Carrying out dispensing activities as per applicable procedure.
Responsible for recording the observation of reaction parameters on the batch card as per approved procedure.
Filling of all the batch card (production cleaning) as per approved instruction.
Ensure verification of pH meters and weigh balances as per applicable procedures.
Maintain work procedure, safety precaution, and cGMP.
Ensure housekeeping of plant and cleanliness of the equipment, update the equipment.
Report accidents and irregularities at the work station to the Shift Officer.
Prepare the production batch card, protocol and other relative documents of production.
ERP operation related to production activities.
Carrying out batch processing including raw material charging, unloading of material and sampling activities during intermediate production.
Coordinating with QA for Online compliance of GMP at shop floor.
All other production-related activities advised by the Superiors from time to time.

Your experience and qualifications

B.Sc./M.Sc. (Chemistry) / Diploma (Chemical Engineering)
2 years

Already Working @TEVAIf you are a current Teva employee, please apply using the internal career site available on Employee Central . By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career SiteThe internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.Tevas Equal Employment Opportunity CommitmentTeva Pharmaceuticals is committed to equal opportunity in employment. It is Tevas global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Keyskills :
batch processing gmp compliance equipment maintenance production documentation erp operations safety chemical engineering cgmp production activities shift officer

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