- Responsible for review and approval of experimental data provided by microbiological tests on raw materials and finished products and on environmental controls.
- Responsible for Analytical Documentation.
- Guarantees the compliance of microbiological analytical data generated with cGMP requirements.
- Supports the QA/Qualified Person about the redaction of SOPs, analytical monographs, validation documentation and all other procedures and activities which could affect, to any extent, the microbiological final product quality.
- To manage the audits of Customers and Health Authorities and written and verbal Responses.
- To qualify the new suppliers.
- To plan the yearly Microbiological Quality Control budget.
- To organize internal professional update courses.
- Ensure that organization's Quality Management System is fully applied within the area of responsibility maintaining total compliance to current GMP, GDP, Data Integrity requirements.
- Ensure adherence to environment, health and safety company requirements as well as legal obligations.
- Behave according to company Ethical Code and company values.
- English (level of proficiency)
- Local language capability in order to communicate to all levels in the sites
- Canteen
- Working flexibility for Caregivers and parents
- Coffee Key
- Recognition Program
- Wellbeing Digital Platform
- 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)
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Quality Control Microbiology Manager - Santhià, Italia - Teva Pharmaceuticals
Descrizione
Who we are
Teva, world leader with over employees, in the field of equivalent medicines, with a differentiated business that also includes specialist medicines, over-the-counter drugs and the production and marketing of APIs (active pharmaceutical ingredients), is present in Italy for over 25 years with a commercial branch and manufacturing sites.
Our mission is simple: improve the wellbeing of our patients.
We care about them and about our colleagues, creating a respectful, diverse and inclusive working environment, committing ourselves to maintaining high standards of quality, compliance and safety, always respecting our values:
We all work for one company and we work together to achieve a common goal.
Main responsibilities and activities
In the Santhià Quality Department we are looking for a brilliant profile reporting to the Site Quality Head with the following responsibilities and activities for the microbyological analysis of all the Italian TAPI sites (Caronno, Villanterio, Rho and Santhià):
Manage Data
Manage microbiological analytical data
Supports the QA/Qualified Person
Management of people
Complying with the Human Resources Policies, the role improves motivation and professional competence of employees.
Requirements
Main requirements:
Education:
Biology University Degree or equivalent Degree
Languages:
Experience:
Minimum: 5 years in microbiological analyses.
What we offer?
We try to take care of our employees, offering them small and large benefits. By way of example:
Type of contract: long term contract
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.
