DSP QA Officer
Contracting – Brabant Wallon
Your responsibilities:
Identical to USP QA Officer, but here we focused on Downstream processes such as purification, chromatography, UF, etc:
* Review paper and electronic batch records line by line.
* Validate data entries, timestamps, and operator actions.
* Ensure deviations and alarms are properly documented.
* Conduct field checks (logbooks, IT systems).
* Collaborate with production and compliance teams.
* Support training and coaching of operators on deviation initiation.
Your profile:
* Minimum 5 years of experience, with strong production experience.
* Experience in pharma is a must.
* Experience in Downstream biomanufacturing.
* Batch record and deviation review expertise.
* Production background (Quality profile who has worked in production quality).
* French fluency.
* On-site availability.
* Proactive and communicative personality.
Nice to have:
* English proficiency.
* QA experience in production.
* Ability to coach operators.
Our offer:
Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. You're interested in this job? We kindly invite you to apply or send me your CV,