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.
Main responsibilities and activities
In the Quality Compliance Department we are looking for a brilliant profile reporting to the Quality Compliance Manager with the following responsibilities and activities:
1. Supports the management of Regulatory audits, self-inspections and customer audits.
2. Support the inspection readiness of the site performing the assigned duties, as shop-floor rounds, capa plan prepararion and CAPA follow up.
3. Support the manager in issuing and reviewing the site GMP and QMS documents, as SMF, SOPs, QC documents.
4. Carry out specific risk management activities and risk assessments according to company procedures and applicable regulations.
5. Support the manager in drafting and reviewing documents shared with clients as QTA, declatation, questionnairs.
6. Support activities aimed to identify and solve possible product quality and registrations issues.
Requirements
Main Requirements:
7. Degree in a scientific discipline (Chemical, CTF or similar)
8. At least 3 years of experience in the pharmaceutical industry with QA topics
9. Previous experience in QC or Regulatory is a plus
10. Fluent English and Italian oral and written communication
11. Computer skills (word, excel, power point, LIMS, TW)
Soft skills:
12. Good verbal and written communication skills
13. Problem-solving skills and result orientation
14. Proactive, teamwork skills and flexibility
15. Able to work with a good level of autonomy with supervision where necessary
What we offer?
We try to take care of our employees, offering them small and large benefits. By way of example:
16. Canteen
17. Working flexibility for Caregivers and parents
18. Coffee Key
19. Recognition Program
20. Welfare Platform
21. Health agreement with medical centers of excellence
22. Flexible working environment (2 days home office per week)
23. Highly inclusive and multicultural working environment
24. Continuous learning and development programs (with full access to Linkedin Learning!)
Type of contract: long term contract
Location and working program
Rho (MI), 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.