* Consultancy Mission: freelance OR employee
-Start date: 01/09/2026
-End date : 31/12/2027
* Work location: Braine l'Alleud
The position of Analytical Method Process Expert is opened within the Global QC organization to support a transformation project aiming to harmonize analytical method processes across Braine and Bulle sites. The mission focuses first on building a standardized process (target by end of the year), then on converting and aligning existing analytical methods into this new framework. It combines process design, documentation work, and cross-site collaboration.
Team info :
The consultant will join a small project-oriented team (3 people including the manager) within a large Global QC organization (several hundreds of people). The team mainly works on process improvement projects rather than routine activities, with strong interaction with laboratories, QC experts, LIMS specialists, and quality representatives.
A typical day will include:
Numerous meetings and discussions with QC laboratories, SMEs, and LIMS stakeholders to understand needs and define processes.
Translating discussions into structured documentation and analytical procedures.
Supporting alignment between sites and contributing to harmonization decisions.
Overall, the role is split between coordination/interaction and strong documentation writing activities.
Requirements
Around minimum 5 years of experience.
Background in QC laboratory environment required (broad understanding rather than deep specialization in one technique).
Must have :
-Experience in QC laboratory environments (GMP context preferred).
-Strong analytical mindset and ability to synthesize complex inputs into clear procedures.
-Excellent writing and documentation skills (key part of the job).
-Ability to interact with multiple stakeholders and manage compromises between sites.
-Good communication skills in English and French (written English particularly important).
-Strong collaboration and influencing skills across teams/sites.
-Organizational skills and ability to work both autonomously and in team.
Nice to have :
-Knowledge or exposure to LIMS systems.
-Experience across multiple analytical domains (HPLC, sterility, cell culture, potency, etc.).
-Experience in process improvement / harmonization projects.
-GMP development experience (not only pure research).
-Project management exposure (support level is sufficient).
Conditions :
* Work life balanceapproximately 2 days onsite / 3 days remote. More onsite presence may be required at the beginning to ensure alignment and onboarding.
* Group insurance
* Hospitalization insurance
* 8 euros meal voucher per day
* Reimbursement km or company car
* Monthly allowance
* A 13th month
* Flex Income Plan
A rate as a freelancer is also possible.