Process Engineer

Teva Pharmaceutical Industries
IT - Lombardia - Rho
July 3, 2024

Who we areTAPI 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 activitiesIn the Manufacturing Department we are looking for a brilliant profile reporting to the Site Production Head with the following responsibilities and activities:
Collects, interprets, analyzes and scientifically reports the data and information relating to the performance of the processes carried out in the production plants to assess whether they remain in a state of control in terms of cycle times, yields and costs.
Ensures and support continuous improvement task for manufacturing processes of commercial products.Executes engineering tasks required by technological transfer of new products/processes from R&D or from other plants and by the implementation of new processes (scale-up, industrialization) for the optimization of existing production processes and for trouble-shooting, collecting and evaluating production results and drawing up technical reports/reports, where necessary.Collaborates with MS&T in identifying operations and critical process parameters and provides technical contribution in operational standardization.Collaborates with site functions in carrying out process validation and cleaning validation activities with constant supervision of field activities.Actively participates by providing technical support to EHS assessments and contributes to the resolution of any identified gaps (for example HAZOP analysis of production processes, CAPA EHS, etc.).Follows/executes technological tests in collaboration with MS&T or external technical companies, verifying the progress of the results and compliance with the programs.Provides and/or collaborates in the development of the engineering documentation necessary for the definition of technical and functional specifications of new equipment and process lines (PFD, URS, etc.) or for modifications to existing ones, even with the help of process simulation software.Supports and collaborates in complex investigations to identify the appropriate root case and establish the appropriate CAPAs.RequirementsMain Requirements:
Quality Management Systems (GMP, GDP and Data Integrity standards) knowledge, to be applied in all work activities where these standards are required.Knowledge and compliance with Environment, Health and Safety (EHS) regulations.Respect for the Code of Ethics and company values.Italian and English knowledge.Education:

Bachelor Degree in Chemical Engineering or Industrial Chemistry.Experience:

At least 3 year experience in chemistry / pharmaceutical chemistry industry (preferred GMP environment) or engineering companies.
What we offer?We try to take care of our employees, offering them small and large benefits.
By way of example:
CanteenWorking flexibility for Caregivers and parentsCoffee Key Recognition ProgramWellbeing Digital Platform Welfare PlatformHealth agreement with medical centers of excellenceHighly inclusive and multicultural working environmentContinuous learning and development programs (with full access to Linkedin Learning!)Type of contract:
long term contractLocation and working programRho (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.

Read the full job description and apply online on the recuiter's web-site

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