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Process engineer

Waterford
Sanofi
Process engineer
€60,000 - €80,000 a year
Posted: 24 August
Offer description

Process Engineer

* Location Waterford
* Fixed Term Contract


About Waterford


For more than 20 years, our Waterford team has continued to grow and diversify to serve patients around the world. Today, a team of almost 800 work together at a state-of-the-art biopharmaceutical and medical device campus. Recognised through multiple local and national awards, Sanofi Waterford offers flexible working and access to a world of opportunities to grow your career at one location. As well as attractive benefits, the team enjoy access to an onsite gym and medical centre that underpin a strong commitment to health and wellbeing.

As Process Engineer you will be responsible for:

Main responsibilities:

* Provide process engineering support to the Lyo APU.
* Support delivery of continuous improvement projects to existing equipment.
* Work closely with various departments, such as MSAT, Technical Development, Quality Assurance, and Supply Chain.
* Lead and coordinate elements of an automated inspection project and contribute to process engineering activities related to the development of new and existing manufacturing capacity.
* Utilisation of knowledge gained from existing manufacturing technologies to aid in the development of new technologies with the goal of implementing higher output and yield.
* Ensure safety compliance, providing technical and engineering support for process and equipment failures, identifying, and implementing process and product improvements, supporting qualification of new products/processes, analysing machine performance data, and managing improvement projects within budget and time constraints.
* Support new product introductions and capacity expansions, including new vendor selections, maintenance planning, design changes, change controls, OEE improvement, yield improvement, etc.
* Lead systematic technical root cause investigations, Customer Complaints, Vendor Complaint, Change Controls and annual PQR Reports.
* Support all company safety and quality programs and initiatives.


About you

* Experience in a highly regulated GMP environment.
* Degree in an Engineering discipline.
* Strong problem solving and communication skills.
* Strong documentation/protocol generation and execution skills.
* Background in high volume inspection with demonstrated experience.

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