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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.
Main responsibilities and activitiesIn the Microbiological Quality Control Department we are looking for a brilliant profile reporting to the Quality Control Microbiology Manager with the following responsibilities and activities:
Use all the Individual and Collective Protection Dispositive, in line with the EHS indications.Respect all the department's safety rules.Maintain a clean and tidy work environment (Housekeeping). Perform sampling of air, water, samples from manufacturing.Perform microbiological tests on Raw materials, Intermediates and Cleaning validation samples, according to the official analytical methods in aseptic conditions.Use the Smarteam system in order to consult the effective analytical methods.Report all the results on Laboratory Notebooks and / or Analytical Sheets according to the relevant procedures.Verify the obtained results in line with the official procedures.Review results read by peers. Use the StarLims system for results collection.Communicate immediately to the direct Supervisor any analytical problem and/or unexpected result.When necessary, use the TrackWise system in order to initiate an analytical investigation.Collaborate with the colleagues in order to maximize the laboratory productivity. Manage all the analytical solutions at the end of the activities (including deactivation).Perform the periodical internal verification on the analytical instruments used in the laboratory.Able to solve the basic problems on the analytical instruments (troubleshooting).Perform some "ancillary" activities useful for the laboratory (for example reagents receiving and labelling).Analytical sample receiving, registration and management. Ensures compliance with the department's safety regulations.RequirementsEducation:
University degree in Biology or CTF
Skills:
Knowledge of all the most common microbiological techniques for samples by manufacturing, environment, air, water, surfaces, personnel, etc.Work in aseptic conditionsFamiliar with informatics systems (Windows, Office)Precision and Accuracy in the activitiesLanguages:
English (basic) and Italian fluent
Minimum Experience / Training required:
Minimum 3-year experience in Microbiological Laboratory of QC or equivalent
What we offer?We try to take care of our employees, offering them small and large benefits. By way of example:
CanteenWorking flexibility for Caregivers and parentsCoffee KeyRecognition ProgramWelfare PlatformHealth agreement with medical centers of excellence Highly inclusive and multicultural working environmentContinuous learning and development programs (with full access to Linkedin Learning!)Type of contract: long term contract
Location and working programTeva's commitment to equal opportunitiesTeva is committed to equal opportunities in the world of work. Our global policy requires equal employment opportunities to be provided regardless of age, race, religion, health, identity, gender expression, protected categories or any other legally recognized status that is entitled to protection under applicable laws.
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