Process Engineer Pharmaceutical Industry
Job in
5830, Boxmeer, North Brabant, Netherlands
Listed on 2026-07-10
Listing for:
TMC
Full Time
position Listed on 2026-07-10
Job specializations:
-
Engineering
Quality Engineering, Process Engineer, Validation Engineer, Pharma Engineer
Job Description & How to Apply Below
You will be responsible for the engineering, installation, commissioning, and qualification of manufacturing equipment within the Project BOND Beta Lactam Formulation Area. The scope includes Beta Lactam formulation vessels, an API powder handling isolator, downflow booths, and auxiliary equipment. While most of the design and construction activities have been completed, key challenges remain in final design optimization, automation integration, installation, commissioning, and qualification.
Working within a multidisciplinary matrix organization, you will collaborate closely with engineering, operations, and project delivery teams to ensure a safe, compliant, and successful project handover.
Key Responsibilities
Act as the technical owner for the Beta Lactam Formulation Area.
Lead remaining design and integration activities for manufacturing equipment.
Provide technical leadership during installation, commissioning, and qualification.
Serve as Subject Matter Expert (SME) for formulation equipment and processes.
Collaborate with GES, DMMD, end-users, and project stakeholders.
Support Factory Acceptance Tests (FATs) at supplier locations.
Build and maintain relationships with engineering and construction partners across Europe.
Ensure Quality, Safety, and GMP compliance throughout project execution.
What We Expect From You
Bachelor's or Master's degree in Process, Mechanical, Industrial (Bio)
Pharmaceutical Engineering, Food Technology, or a related discipline.
5+ years of experience in pharmaceutical, biotech, food, or high‑tech capital projects.
Experience with hygienic design, powder handling, and Beta Lactam processing is an advantage.
Knowledge of GMP, EU GMP Annex 1, EHEDG, and ISPE guidelines.
Understanding of pharmaceutical or food manufacturing facilities and equipment integration.
Strong stakeholder management and communication skills.
Fluent in English;
Dutch is a plus.
Willing to travel to supplier locations when required.
Available on‑site in Boxmeer at least three days per week; full‑time presence expected during critical project phases.
What You Can Expect From Us
We offer a challenging and stimulating work environment in which you can have autonomy over your career. We value technical expertise and foster a culture of innovation and engagement.
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