Msat lab scientist (España)

Msat lab scientist (España)

01 ago
|
Nalys
|
España

01 ago

Nalys

España

MSAT Lab Scientist — Upstream Bioprocessing | Biopharmaceutical Manufacturing

?Brabant wallon, Belgium

About Nalys

Nalys is a fast-growing consultancy company specialized in high-tech engineering and life sciences. Founded 15 years ago, we partner with leading organizations to deliver innovative solutions and expert support across a wide range of technical domains. At Nalys, we believe in combining deep expertise with a human-centric approach — empowering our consultants to thrive and our clients to succeed. Joining Nalys means becoming part of a collaborative, agile, and forward-thinking team that values excellence, innovation, and continuous growth.

The Mission

Bioreactors don't run themselves — and neither does the science behind them. We're looking for an MSAT Lab Scientist to join a Bio Manufacturing Sciences & Technology team supporting commercial biologics production in Belgium, on a high-priority short-term project where hands-on expertise and fast autonomy make the difference.

Your Responsibilities

- Run and monitor upstream bioreactor experiments, from setup to data capture
- Prepare media and support day-to-day laboratory activities tied to manufacturing
- Manage and optimize small-scale models representative of full-scale processes
- Analyze experimental and manufacturing data, applying statistical methods to interpret results
- Draft technical documents, protocols, reports, and GMP-compliant records, including investigation and deviation support
- Contribute to technology transfer and process validation activities
- Collaborate closely with MSAT scientists, manufacturing teams, and cross-functional stakeholders on continuous improvement initiatives

Your Profile

- You bring solid experience in Upstream Processing (USP)



and hands-on bioreactor operation
- You've worked in a biopharma or biotechnology environment and are comfortable running experiments independently
- You write clearly and precisely — protocols, reports, and GMP documentation are second nature to you
- You're at ease in a cGMP/GxP setting and understand what compliance means in practice
- You have real experience analyzing data and drawing sound conclusions from it
- You communicate well and work naturally across teams and disciplines
- You hold a Master's degree in Biotechnology, Biology, Chemical Engineering, or a related scientific field
- You can juggle multiple priorities without losing sight of quality
- Fluent English is required; French is a strong asset for local collaboration
- Familiarity with JMP, R, Python, or similar statistical tools is a plus, as is prior exposure to technology transfer or validation projects

What We Offer

- A human‑scaled consulting company focused on expertise, partnership, and career development
- Long‑term assignments with leading pharmaceutical players
- Continuous learning through technical coaching, training, and knowledge sharing
- A supportive culture that values autonomy, trust, and impact.

The recruitment process

By applying for the "Project Scheduler" position, you will go through the following steps in our recruitment process:

1. Olivia Braszko, TA Specialist, will analyze your resume and schedule a first screening.
2. You will have a second interview with our Technical Director, Yves Le Goff, and the TA Specialist
3. The last interview will be with our Business Unit Director, Jimmy Rousseaux.

Interested?

? Apply directly via this post and let's discuss your motivation through a first teams meeting!

📌 Msat lab scientist (España)
🏢 Nalys
📍 España

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