Teva Pharmaceuticals Senior Project Engineer in Santhia, Italy
Senior Project Engineer
Date: Nov 24, 2022
Location: Santhia, IT, 0000
Company: Teva Pharmaceuticals
Who we are
Teva, world leader with over 40.000 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:
Teva Code of conduct
We all work for one company and we work together to achieve a common goal.
Site Engineering Head
Main activities and responsibilities
Manage all aspects of multiple related projects to ensure the overall program is aligned to and directly supports the achievement of strategic objectives.
Report on project success criteria results, metrics, test and deployment management activities.
Work creatively and analytically in a problem-solving environment demonstrating teamwork, innovation and excellence.
Defines the User Requirements and translate them into the project documents: P&LD, Lay-out, Data Sheet, Mechanical and electro-instrumental Work requisitions.
Prepare estimates and detailed project plan for all phases of the project.
Management of all the project phases from Concept and User Requirements (agreed with the stakeholder) till the commissioning and qualification phases (IQ/OQ/PQ) in conformity with EU GMP.
Management of project Design Change with consequent impact analysis (cost, timing, safety, GMP).
Aligns offers from a technical point of view and arranges them financially, to allow the Purchasing department to proceed with the commercial negotiations.
Defines and keeps under control the GANTT of the assigned projects, ensuring that deadlines are met in line with quality requirements.
Coordinates the start-up and qualification activities of new systems and equipment.
Finalize Commissioning, Qualification and Validation (CQV) strategy and execution plans for all site activities.
Be accountable for schedule, costs and customer quality expectations.
Coordinate commissioning and qualification engineers, personnel provided by contractors as well personnel from vendors of complex equipment / packages.
Support the finalization of the necessary documentation / protocols to be used during site activities.
Manage all aspects and priorities of most related Hazop on production process lines.
CAPA activities Near Miss/Accidents.
CAPA activities by Corporate risk assessment.
DVR Improvement Plan.
at least 7+ years in similar roles
What we offer?
We try to take care of our employees, offering them small and large benefits. By way of example:
Wellbeing Digital 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: 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 or gender expression, or any other legally recognized status that is entitled to protection under applicable laws.
EOE including disability/veteran