Physico-Chemical Analytics Project Assistant

Scientific Project Assistant – Physico-Chemical Analytics Sector : Biopharma

Location:
Brabant-Wallon Contract Type: Full-time (Employee or Freelance via Randstad Professionals) About the Opportunity Are you an experienced pharmaceutical professional with a strong background in analytical sciences, looking to step away from the bench and into a strategic, project-driven role? At Randstad Professionals, we connect top talent with industry leaders. We are currently looking for a PCA (Physico-Chemical Analytics) Project Assistant to consult for our client, a leading global biopharmaceutical company. In this role, you will provide critical support to an experienced Project Lead within the Analytical Development Sciences department. Your Responsibilities As a key contributor to the project team, you will act as a scientific documentation expert and project coordinator. Your daily responsibilities will include:
- Scientific Documentation: Preparing, editing, and reviewing analytical methods, protocols, reports, presentations, and regulatory supporting documents.
- Quality Management: Managing and contributing to change controls, deviations, CAPAs, and risk assessments.
- Data Review: Reviewing analytical results provided by external partners to ensure accuracy and compliance.
- Cross-Functional Collaboration: Interacting seamlessly with a network of ~15 key stakeholders across QA, QC, Regulatory Affairs (RA), MSAT, and Manufacturing teams.
- Regulatory Support: Assisting in the preparation of regulatory submissions and facilitating knowledge transfer activities.

Your Profile
We are looking for an experienced, highly autonomous profile ready to make an immediate impact (limited training required).
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Experience:
Minimum 3 to 5 years of experience in the pharmaceutical or biopharmaceutical industry.
- Technical Knowledge: Strong theoretical background in physico-chemical analytical techniques applied to proteins (SEC, RP, Affinity, IEX, HILIC, HIC) and/or capillary electrophoresis techniques (CE, CGE, iCE, MauriCE). You must be able to confidently understand and discuss analytical methods.
- Documentation & Quality: Proven experience in preparing scientific/analytical documentation under GMP/GLP environments.
- Soft

Skills:
Proactive, autonomous, and equipped with excellent communication skills to navigate a complex, cross-functional matrix.
- Languages: Fluency in both English and French is strictly mandatory. Bonus Points (Nice-to-haves):
- Direct experience supporting regulatory submissions or handling Health Authority requests.
- Background in Quality Assurance (QA) environments or analytical method development/validation.
- Familiarity with electronic Quality Management Systems (eQMS) and document control platforms.

What We Offer
- A stimulating assignment through Randstad Professionals (available for both freelance consultants and employees).
- A full-time position with a flexible hybrid working model. Ready for your next challenge? If you have the scientific background and the project management mindset we are looking for, we want to hear from you Apply now to join Randstad Professionals via Mehdi Soli : mehdi.soli.soli@randstad.be