Project responsible – dsp

Project Responsible – DSP | Purification & Lyophilisation

Brabant wallon, Belgium

Introducti

on
Behind every successful batch lies a team of rigorous, hands-on scientists who bridge the gap between R&D and GMP production — and that's exactly the role we're looking to fi

ll.
About Nalys G

roup
Nalys Group is a Belgian recruitment and consultancy firm specialised in the pharmaceutical, biotech and life sciences industries. We connect expert talent with leading organisations across Belgium and France, supporting both candidates and clients with tailored, hands-on expertise at every step of the jou

rney.
On behalf of a leading pharmaceutical manufacturing site in the Brabant wallon area, Nalys is recruiting a Project Responsible – Downstream Processing (DSP), with a focus on purification and isolation

steps.
Your Responsib

• ilities Develop and optimise DSP processes at laboratory scale, with a critical eye on scale-up performance (purification, desalting, concentration, evaporation, filtration, lyophilisation, spray
• -drying)Coordinate large-scale production campaigns (pre-PPQ and PPQ): planning, consumables ordering, operator training, on-site supervision and post-campaign batch recor
• d reviewWrite, partially review and finalise Batch Records and Master Batch Records; update SOPs, flow charts, BOMs and campaign reports in full compliance with cGMP requ
• irementsInitiate and manage deviations, investigations and CAPAs; implement change controls in collaboration
• with QAAct as the scientific and technical reference for your process scope, contributing to R&D protocols and manufacturing docum
• entationParticipate actively in Operational Excellence initiatives (6S, standard plans) and cross-functional interactions with QA, QC, Supply, Engineering and Main

tenance.
You

• r Profile You hold a degree in chemistry, biochemistry, pharmaceutical sciences or chemical e
• ngineeringYou have hands-on experience in a GMP pharmaceutical e
• nvironmentYou are familiar with DSP unit operations: chromatography, lyophilisation, filtration and/or sp
• ray-dryingYou are comfortable managing GMP documentation (BRs, SOPs, deviations, CAPAs) au
• tonomouslyYou are a self-starter who thrives in a dynamic production environment, able to manage multiple priorities simu
• ltaneouslyYou communicate fluently in both English a

nd French.
Wh

• at We Offer A human‐scaled consulting company focused on expertise, partnership, and career
• developmentLong‐term assignments with leading pharmaceut
• ical playersContinuous learning through technical coaching, training, and knowl
• edge sharingA supportive culture that values autonomy, trust
• , and impactAn attractive salary package with addition

al benefits.
Our Recrui

tment Process
When applying for this position at Nalys, you can expect a clear and engaging recrui

• tment journey: Talent A

cquisition CallA first discussion with our Talent Acquisition Specialist, Olivia Braszko, to understand your background, motivations, a

• nd career goalsTech

nical InterviewA meeting with one of our Technical Referent to evaluate your expertise and fit

• for the missionBus
• iness InterviewA conversation with the Business Unit Director, Jimmy Rousseaux, to discuss the project context and your futur

e within Na

lys.
Interested? Apply directly via this post and let's discuss your motivation through a firs