Analytical Scientist

Johnson & Johnson; Beerse; Sur place; EUR 68 880 - 96 432; Plein temps

Avantages offerts par ce poste

Competitive hourly rate

Résumé du poste

Johnson & Johnson is seeking a Scientist for their Analytical Method & Stability Center in Beerse. This role involves supporting multiple projects in synthetic development and initiating stability studies for drug products.

Candidates should hold a PhD or a Master's degree with relevant experience, alongside knowledge of regulatory industry standards. Strong communication skills and the ability to collaborate are essential for this position.

Qualifications

• 0–3 years of proven experience for PhD holders or at least 3 years for Master's degree.
• Knowledge of ICH, RIBPS, and stress studies on synthetic compounds.
• Industry experience with GMP regulations.

Responsabilités

• Support multiple assigned projects in synthetic development.
• Collaborate with Analytical Development teams and product development.
• Initiate fit-for-purpose stability studies and provide scientific data interpretation.

Connaissances

Knowledge of various stability studies

Technical knowledge for developing analytical methods

Experience with synthetic drug substances

Ability to work independently and in a team

Excellent communication skills

Formation

Advanced scientific degree (PhD) in Analytical Chemistry or related

Master’s degree in chemistry, biochemistry or related field

Outils

Liquid chromatography

Description du poste

Scientist – Analytical Method & Stability Center

Location: Beerse

Duration: 12 months

Hours: 40 hours per week

As a Scientist within the Analytical Method & Stability Center (AMSC), you will join Analytical Development, part of the Therapeutics Development & Supply organization within J&J Innovative Medicine. AMSC is a diverse, highly engaged team that supports analytical method development, clinical release, and stability assessment for synthetically designed drugs across the full product lifecycle—from early development through commercialization.

Roles and Responsibilities

• Independently support multiple assigned projects in synthetic development (including oligonucleotides, peptides, conjugates, degraders, etc.) and establish priorities in line with project- and team objectives/deliverables.
• Collaborate closely with colleagues in other Analytical Development teams, API and drug product development.
• Initiate fit-for-purpose stability studies and characterization techniques, providing deep scientific data interpretation to impact product development.

How to Succeed – Education & Qualifications

Education: Advanced scientific degree (PhD) in Analytical Chemistry, Pharmaceutical Technology or related science with 0–3 years of proven experience. OR a master’s degree in chemistry, biochemistry or related field with at least 3 years of relevant experience.

Experience and Skills

• Knowledge of various stability studies (ICH, RIBPS, open dish stress studies) on synthetic compounds.
• Technical knowledge for developing, validating and transferring analytical methods with major focus on liquid chromatography.
• Experience with synthetic drug substances (conjugates, oligonucleotides, degraders) and formulation processes and required analytical techniques.
• Industry experience and knowledge of GMP regulations.
• Ability to work independently and in a team environment.
• Professional project oversight with respect to deadlines and urgency.
• Excellent communication skills and proactive attitude.
• Results and performance driven.

Benefits

This role offers a very competitive hourly rate. The position is primarily on‑site and is a 12‑month contract.

Diversity, Equity & Inclusion

We are committed to creating an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each person feels they belong and can reach their potential.

(The company is an equal‑opportunity employer and complies with all applicable laws.)