Teva TAPI - Quality Compliance Sr Specialist 

Italy, Lombardy 

868056375

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.
• Support the inspection readiness of the site performing the assigned duties, as shop-floor rounds, capa plan prepararion and CAPA follow up.
• Support the manager in issuing and reviewing the site GMP and QMS documents, as SMF, SOPs, QC documents.
• Carry out specific risk management activities and risk assessments according to company procedures and applicable regulations.
• Support the manager in drafting and reviewing documents shared with clients as QTA, declatation, questionnairs.
• Support activities aimed to identify and solve possible product quality and registrations issues.

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
• Computer skills (word, excel, power point, LIMS, TW)

Soft skills:

• 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

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

Rho (MI), from Monday to Friday