Tapi - Quality Compliance Sr Specialist Rho

Tapi - Quality Compliance Sr Specialist
Rho
Lombardia, Rho

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. This 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. 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 Compliance Department, we are looking for a brilliant profile reporting to the Quality Compliance Manager with the following responsibilities and activities: Supports the management of Regulatory audits, self-inspections, and customer audits. Supports the inspection readiness of the site performing the assigned duties, including shop-floor rounds, CAPA plan preparation, and CAPA follow-up. Supports the manager in issuing and reviewing the site GMP and QMS documents, such as SMF, SOPs, and QC documents. Carries out specific risk management activities and risk assessments according to company procedures and applicable regulations. Supports the manager in drafting and reviewing documents shared with clients, such as QTA, declarations, and questionnaires. Supports activities aimed at identifying and solving possible product quality and registration issues. Requirements Main Requirements: Degree in a scientific discipline (Chemical, CTF, or similar). At least 3 years of experience in the pharmaceutical industry with QA topics. Previous experience in QC or Regulatory is a plus. Fluent English and Italian oral and written communication. Good verbal and written communication skills. Problem-solving skills and result orientation. Proactive, teamwork skills, and flexibility. 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: Canteen Working flexibility for caregivers and parents Coffee Key Recognition Program Welfare Platform Health agreement with medical centers of excellence Flexible working environment (2 days home office per week) Highly inclusive and multicultural working environment 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. J-18808-Ljbffr