Senior Engineer Tech Transfer

Location Beerse
Discipline: Pharmaceutical
Contact name: Ivor Duif

Contact email:
Job ref: 10481
Published: 6 months ago


For one of our big pharma clients we are looking for a Senior Engineer Tech Transfer!

The Senior Engineer will collaborate closely with other NPI, engineering and Subject Matter Expert (SME) functions in the D&P CoE, the site and the Primary Container and Device Development (PC&D) organization for successful introduction and qualification of the new device and packaging components and corresponding assembly and packaging processes in the commercial supply chain.


For this diversified position we are looking for a team player with strong organizational and project skills.  A good candidate is capable of navigation through complex topics, has the professionalism to communicate in a correct and timely manner and continuously demonstrates a strong mindset to deliver on deadlines.


-            Process development for device assembly and packaging.

-            Commercialization activities including process and equipment qualification (IQ/OQ/PQ),

-            Verification and validation of test process and test fixtures to meet targeted test coverage and


-            Preparation and oversight of packaging development activities including preparation and organization of transportation studies.

-            Collection and analysis of test data to identify problems, optimize processes and drive continuous process improvements including feedback to suppliers, manufacturing and development engineering.

-            Collection of design transfer documentation for consideration within the Design History File

-            Collaborating with site operations, supporting any improvements to the processes and/or equipment, to ensure reliability at the highest possible levels



Hard Skills

-            A minimum of a Master degree in Engineering and/or a scientific degree or equivalent combination of education and work experience.

-            Experience with FDA regulated Design Control, Change Control and ISO 13485, Medical devices – Quality management systems – Requirements for regulatory purpose, European Medical Device Directive is required.

-            A minimum of 5 years of experience in combination products or medical device manufacturing, assembly, packaging and/or Research & Development (R&D).

-            Broad scientific or engineering expertise with demonstrable results to deliver new products or sustain existing marketed products is required.

-            Fluent in both Flemish and English


4 months