Job description
Do you dare to shake up the medical world and improve the lives of patients with chronic degenerative diseases?
Allegro is a revolutionary start-up that designs and develops ground-breaking biomedical nanotechnology for the treatment of osteoarthritis.
Role Description
This is a full-time role for a Industrial Manufacturing and Engineering Manager. As an Industrial Manufacturing and Engineering Manager, you will be responsible for production runs and upscaling (lab to pilot), performing analytical tests, maintaining laboratory equipment, and performing quality control. This is an on-site role where you will work in our laboratory facilities in Liège.
Qualifications
Manufacturing operations in cleanroom environments (ISO 8) – being hands‑on!
Equipment qualification and requalification (IQ/OQ/PQ)
Process validation and cleaning validation
Calibration and maintenance programs
Raw material handling, traceability, and inventory management
Execution of QC testing with analytical equipment and batch release testing
Implementation of sampling plans
Operational implementation of packaging and sterilization activities
Execution of stability studies (pulls, testing, trending)
ERP, logistic and packaging/labelling knowledges
Experience in organic chemistry
Analytical skills for analyzing test results and interpreting data
Strong attention to detail and accuracy in documentation
Key regulatory and standards knowledge expected
EU MDR 2017/745 (operational application)
ISO 13485 (manufacturing, documentation, batch records, GDP)
ISO 14644 (cleanrooms)
ISO 11737 (bioburden, endotoxins, sterility testing interface)
ISO 11607 (packaging validation and routine controls)
ASTM F3127 (cleaning validation)
ASTM F88 / F1886 / F1929 / F2096 (packaging integrity & seal testing)
Profile
Hands‑on! You are willing to work in the production, besides the QC part.
Practical experience in synthetic organic chemistry
Experience in characterization methods, analytical chemistry and processing techniques
Knowledge of biopolymers and hydrogels
Good knowledge of the English language, spoken and written
Proven experience in the medical device industry
Solid understanding of ISO 13485 and EU MDR 2017/745
Ability to think and act in a medical device regulatory mindset
Comfortable working in small teams with high autonomy and responsibility
Strong project management skills combined with a hands‑on mindset
We offer
We offer great career opportunities for ambitious people within a thriving environment. We offer a very competitive remuneration package and various fringe benefits:
Competitive salary package
Meal vouchers
Hospitalisation Insurance
State‑of‑the‑art working tools
Contributing to groundbreaking medical technology
Working with a great team
Expand your knowledge through internal training
Personal and professional development process
Please apply through LinkedIn or send your CV+cover letter to hr@allegro.bio. We look forward to meeting you soon!
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