C&Q Project Lead – API Manufacturing Equipment
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Job Location:
Monthly Salary:
Posted on:
10 hours ago
Vacancies:
1 Vacancy
Job Summary
C&Q Project Lead API Manufacturing Equipment
Location: Flanders
Type: Full-time
What youll be doing
Lead a high-visibility pilot project focused on API manufacturing equipment. Youll take ownership of commissioning and qualification activities providing technical direction and delivering tangible results. Your strong PM competences will keep stakeholders aligned while your technical know-how ensures quality execution.
Whats in it for you
Make a real impact: Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma biotech and medical devices
Grow within a community of experts: Benefit from knowledge-sharing mentoring and exposure to diverse challenging assignments that broaden your expertise.
Build a meaningful career: As an ambitious and pioneering company we want to offer you the best possible environment to thrive within the life sciences.
A fair competitive package: We offer tailored transparent compensation aligned with your expertise preferences and local market regulations because your contribution deserves to be valued.
What you bring
Extensive API production expertise and understanding of chemical processes
Proven commissioning & qualification experience with equipment like reactors dryers filling lines dosing tanks isolators
Strong project management and communication skills
Experience with risk-based approaches (FMEA failure mode analysis)
Hands-on knowledge of Delta V (DCS) and PLC systems
Ownership mindset - you shape content provide direction and deliver
Who you are
You take the bull by the horns and dont wait for perfect conditions
Youre a problem-solver who thrives in complex technical environments
You communicate clearly with both technical teams and management
Youre results-driven and accountable
About us
We support life sciences companies from idea to patient offering tailored solutions in development clinical regulatory compliance production and distribution. With 500 experts across 8 countries we help drive innovation in ATMP biotech medical devices diagnostics digital health and pharma.
We believe in JPEG:
Joy. Partnership. Going the Extra Mile. Getting Things Done.
You wont just be taking a job youll be joining a community where people grow laugh build and contribute to something bigger.
Interested Lets talk.
Send us your CV and motivation letter. You could be the next one to join the QbD family.
