Analytical Scientist (qPCR & ELISA) - Dutch

Jefferson Wells Belgium; Antwerpen; On-site; EUR 70,000 - 100,000; Full time

Job summary

Jefferson Wells Belgium is seeking an Analytical Scientist to join its Manufacturing Science, Analytics & Technology (MSAT) organization in Belgium. The role focuses on development, transfer, validation, and continuous improvement of analytical methods for biologics in a GMP environment.

You will lead qPCR and ELISA methods, transfer from R&D to MSAT and QC, design experiments, write protocols and reports, and ensure data integrity and cGMP compliance.

Qualifications

• PhD or equivalent in Life Sciences, Biotechnology, Biochemistry, Molecular Biology or related field.
• Strong expertise in qPCR and ELISA within biopharma/biotech settings.
• Experience in analytical method development, qualification and validation.
• Knowledge of protein characterization techniques is a plus.

Responsibilities

• Act as SME for qPCR and ELISA analytical methods.
• Lead method transfer from R&D to MSAT with documentation and training.
• Support transfer from MSAT to QC including protocols and reports.
• Design, develop, optimize and validate analytical methods for manufacturing processes.
• Plan and execute analytical studies and DOE experiments.
• Write high-quality protocols and GMP documentation.
• Monitor method performance via data analysis and statistics.
• Investigate deviations and implement corrective actions.
• Present findings to cross-functional teams.
• Provide hands-on lab support for testing activities.

Skills

qPCR

ELISA

DOE studies

Statistical analysis

Problem solving

Project management

Independent work

Technical writing

Education

PhD or equivalent in Life Sciences, Biotechnology, Biochemistry, Molecular Biology

Tools

SDS-PAGE

Western Blot

Southern Blot

Northern Blot

Job description

For our client, specialized in the biopharmaceutical company, we are seeking an Analytical Scientist to join its Manufacturing Science, Analytics & Technology (MSAT) organization. This position offers the opportunity to play a key role in the development, transfer, validation, and continuous improvement of analytical methods supporting the manufacturing of innovative biologic therapies in a highly regulated GMP environment.

Key Responsibilities

• Act as the subject matter expert for qPCR and ELISA analytical methods.
• Lead the transfer of analytical methods from R&D to MSAT, ensuring effective documentation, training, and knowledge transfer.
• Support the transfer of validated qPCR and ELISA methods from MSAT to Quality Control (QC), including troubleshooting activities and preparation of transfer protocols and reports.
• Design, develop, optimize, and validate analytical methods for both existing and new manufacturing processes.
• Independently plan and execute analytical studies and experimental designs.
• Author high-quality scientific protocols, technical reports, and supporting documentation.
• Monitor method performance through data trending and statistical analysis to ensure reliability and robustness.
• Conduct root cause investigations related to analytical deviations and implement corrective actions where required.
• Present scientific findings and recommendations to cross-functional teams and stakeholders.
• Provide hands-on laboratory support for small-scale testing activities.

Profile

• PhD or equivalent experience in Life Sciences, Biotechnology, Biochemistry, Molecular Biology, or a related scientific discipline.
• Strong practical expertise in qPCR and ELISA, ideally within a biopharmaceutical or biotechnology environment.
• Proven experience in analytical method development, qualification, and validation.
• Knowledge of protein characterization techniques such as SDS-PAGE, Western Blot, Southern Blot, or Northern Blot is considered an asset.
• Ability to design and execute Design of Experiments (DOE) studies and interpret complex analytical datasets.
• Strong statistical and data analysis skills, including method performance evaluation.
• Excellent problem-solving and troubleshooting abilities with a scientific and analytical mindset.
• Capable of managing multiple projects simultaneously while working independently.
• Comfortable balancing laboratory-based activities with documentation and data analysis tasks.
• Strong technical writing skills with experience preparing protocols, reports, and GMP documentation.
• Excellent understanding of cGMP requirements and their application to analytical methods and laboratory operations.

Languages

• Fluent in Dutch and English, both written and spoken.

Offer

You will join a cutting-edge biopharmaceutical environment supporting the development and manufacture of next-generation biologic therapies. Working within an international and highly collaborative scientific team, you will contribute to analytical excellence, process innovation, and the successful delivery of life-changing medicines to patients worldwide.