Chemical Quality Control - maternity cover Location: Santhia, Italy, 0000
Job Id: 59606
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. Headquartered 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 activities In the Quality Control Department, we are looking for a brilliant profile reporting to the Quality Control Supervisor with the following responsibilities and activities:
Use 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). Ensure compliance with the department's quality rules (GLP and GMP). Perform the analytical activities, according to the official analytical methods, in line with the received training. Use the Smarteam system to consult the effective analytical methods. Basic knowledge of the most common analytical techniques present in the laboratory, including the software connected to the instruments (stand-alone and/or client-server architecture). Report all the results on Laboratory Notebooks and/or Analytical Sheets according to the relevant procedures. 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 to initiate an analytical investigation. Collaborate with colleagues to maximize laboratory productivity. Manage all analytical solutions at the end of the activities (including deactivation). Perform some ancillary activities useful for the laboratory (for example, reagents receiving and labelling, gas cylinder check, chromatographic columns maintenance). Receive the analytical sample, registration, and management according to the relevant procedures. Requirements Education: Chemical secondary school or University degree in Chemistry, Pharmacy, CTF
Skills:
Familiar with informatics systems (Windows, Office) Collaborative and communicative Precision and accuracy in the activities Languages: English and Italian (level of proficiency)
Minimum Experience / Training required: Scholastic knowledge in Quality Control Laboratory or equivalent
What we offer? We try to take care of our employees, offering them small and large benefits. By way of example:
Canteen Working flexibility for caregivers and parents Coffee Key Recognition Program Welfare Platform Health agreement with medical centers of excellence Highly inclusive and multicultural working environment Continuous learning and development programs (with full access to LinkedIn Learning!) Type of contract: Temporary contract - 12 months
Location and working program Santhià (VC), from Monday to Friday
Teva's commitment to equal opportunities Teva 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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