Young Master Graduate | Reference Standard Owner

Bekijk en reageer bij Pauwels Consulting (externe link)

Reference Standard Owner bij J&J Beerse, fulltime hybride, voor recent afgestudeerden in Life Sciences/QA.

Locatie: Beerse, BE
Werkvorm: hybride
Contractvorm: detachering
Eerste waarneming: 30 augustus 2026
Opdrachtgever: Johnson & Johnson Beerse

Eisen

Structured, ownership-driven and genuinely quality-minded
Spectrometry basics: LC-MS, GC-MS, NMR
Clear communicator — written and verbal, in English
Strong sense of urgency and ability to prioritize under pressure
Strong chromatography skills: LC, UPLC, GC, GC-headspace
Master's degree in Chemistry, Pharmacy, Biochemistry or related scientific field
Wet chemistry knowledge: titrations and related techniques
Analytical mindset with sharp eye for detail and quality

Omschrijving

At Johnson & Johnson Beerse — one of the world's leading pharmaceutical innovators — a dedicated team manages reference standards for small molecule drug products. These standards are the backbone of analytical quality control: without them, no product leaves the site. You'll step into a role with real scientific ownership, working in a GMP environment where precision matters and your contribution is visible from day one. As a Reference Standard Owner, you are responsible for the full lifecycle management of assigned reference standards. You ensure that qualification and requalification activities are executed on time, in compliance with GMP requirements and according to the highest quality standards. You act as a key coordinator between analytical laboratories, quality stakeholders and project teams. Key responsibilities include defining and managing the qualification strategy for assigned reference standards, setting up protocols, coordinating analytical testing and certifying materials on time; issuing Certificates of Analysis (CoA) and registering them in the reference standard management system; assessing requalification results and determining appropriate storage conditions and retest periods; bridging internal labs, external testing partners and quality stakeholders; leading or contributing to deviation investigations, documenting events in TrackWise and driving corrective actions; and contributing to process improvement projects. The profile requires a Master's degree in Chemistry, Pharmacy, Biochemistry or a related scientific field, strong chromatography skills (LC, UPLC, GC, GC-headspace), wet chemistry knowledge (titrations and related techniques), spectrometry basics (LC-MS, GC-MS, NMR), an analytical mindset with a sharp eye for detail and quality, a strong sense of urgency and ability to prioritize under pressure, clear written and verbal communication in English, and a structured, ownership-driven and genuinely quality-minded approach. Recent graduates are strongly encouraged to apply. The offer includes real scientific ownership from day one, a world-class environment, a clear growth path towards senior scientific or quality leadership roles within GMP, and Pauwels Consulting support throughout the assignment.

Alle opdrachten Bekijk en reageer bij Pauwels Consulting (externe link)

Gegevens automatisch overgenomen uit de oorspronkelijke publicatie; controleer de details bij de bron. Wij zijn geen partij bij de aanvraag. Hoe wij werken.