Operator III

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

•    Responsible for issuance of raw material from warehouse as per production requirement storage and labeling as per applicable procedure.
•    Assisting the team leader in ensuring proper storage of raw material, intermediates and finished goods in designated areas and labeling as per applicable procedure.
•    Carrying out dispensing activities as per applicable procedure
•    Carrying out process and sampling activities during the production of intermediate / API’S according to the approved batch cards.
•    Filling of the batch cards (production & cleaning) as per approved instructions and recording the observations and parameters in the batch card.
•    Ensure verification of weigh balances and all daily documents as per applicable procedures.
•    Carrying out the Ph analysis and performing the verification of the PH meter as per applicable procedures.
•    Follow standard operation procedure (SOP), safety and cGMP guideline.
•    Ensure housekeeping of  plant and cleanliness of the equipments/area update the equipment status board, use log book , other documents as per applicable procedure.
•    Batch details put in ERP systems.
•    Preparation of batch card, qualification protocol, report & other GMP related documents.
•    Preparation of safety work permits to carry out maintenance activities in shift.
•    Report accidents and irregularities at the work station to the shift officer.
 

Your experience and qualifications

• B.sc/M.sc/Diploma (Chemical)/B.tech (Chemical)/B.E (Chemical)

• 2--5 Years experience

Already Working @TEVA?

If 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 Site

The 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.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's 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.