Analytical Scientist - LC Method Development (Contract)

Sentior, Ltd.; Beerse; Remote; EUR 55,000 - 83,000; Full time

Job summary

Johnson & Johnson Beerse seeks an Associate Scientist (Medior) to deliver analytical support for new molecular entities from Phase 1 to registration. You will perform method development and validation across drug substances and products, with emphasis on LC and physico-chemical analyses.

You will ensure compliance with regulatory guidelines and GMP, while contributing to high-quality results in a dynamic, tight timeline environment. English proficiency is essential.

Qualifications

• Master’s degree in Chemistry, Pharmaceutical Sciences, Biochemistry or related field, or bachelor’s with 3+ years industrial experience.
• General awareness of cGMP regulations is a plus.
• Strong knowledge of liquid chromatography (LC) and physico-chemical techniques.

Responsibilities

• Deliver analytical support for new molecular entities from Phase 1 to registration.
• Support method development and validation for drug substances and drug products.
• Perform analysis for characterization, method development, validation, release, and stability (LC and physico-chemical).
• Develop fit-for-purpose LC and physico-chemical methods (e.g., Karl Fischer, titration).
• Ensure compliance with regulatory guidelines, GMP, and safety; scientifically evaluate results.

Skills

Analytical chemistry

LC method development

Physico-chemical techniques

Quality standards

English proficiency

Education

Master's in Chemistry/Pharmaceutical Sciences/Biochemistry or related field

Bachelor+3 years industrial experience

Tools

Empower

OpenLab

Tiamo

Omnis

Karl Fischer

Job description

Johnson & Johnson Beerse seeks an Associate Scientist (Medior) to deliver analytical support for new molecular entities from Phase 1 to registration. You will perform method development and validation across drug substances and products, with emphasis on LC and physico-chemical analyses.

You will ensure compliance with regulatory guidelines and GMP, while contributing to high-quality results in a dynamic, tight timeline environment. English proficiency is essential.