Scientist Bioanalytics

TN Belgium; Flanders (CT); On-site; USD 70,000 - 110,000; Full time

Job summary

An established industry player is seeking a Scientist in Bioanalytics to support the implementation of bioanalytical strategies for drug development. This role involves collaboration with project teams and oversight of bioanalytical studies, ensuring compliance with GLP and GCP standards. The ideal candidate will possess a Master's degree in life sciences and have hands-on experience with ligand binding assays. Join a dynamic and rapidly growing biotech company that offers a competitive compensation package and the opportunity to work closely with external partners and the scientific community.

Benefits

Competitive compensation package

Extensive benefits

Dynamic work environment

Qualifications

• Solid knowledge of bioanalytical method development and validation.
• Experience managing Contract Research Organizations (CROs) is an asset.

Responsibilities

• Oversee method transfer and validation to bioanalytical vendors.
• Review bioanalytical sample analysis plans and reports.

Skills

Bioanalytical method development

Ligand binding assays

Communication skills

Regulatory guidelines (GLP and GCP)

Project management

Education

Master's degree in life sciences

Tools

ELISA

MSD

Gyrolab

Job description

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For the expansion of the Bioanalytical team, our client is looking for a Scientist Bioanalytics who supports the implementation and execution of bioanalytical strategies for non-clinical and/or clinical development programs in close collaboration with project teams.

You will be a key representative of the bioanalytical team in one or multiple non-clinical/clinical teams and will be involved in different phases of drug development.

You should have solid knowledge of scientific and regulatory requirements for bioanalytical method development and validation for PK, PD, and/or immunogenicity assays. Hands-on experience with ligand binding assays and strong communication skills are considered assets.

As a bioanalytical study monitor, your responsibilities include method transfer and validation to bioanalytical vendors, overseeing BA study phases (GLP and GCP) of non-clinical/clinical studies, in collaboration with the project team and bioanalytical project manager.

• Review of method validation plans and reports
• Review of bioanalytical sample analysis plans and reports for non-clinical and/or clinical studies
• Review and input on clinical trial documents (protocols, reports, data transfer agreements, lab manuals, etc.) and regulatory documents
• Support the development of bioanalytical strategies in collaboration with bioanalytical, project, and clinical teams
• Initiate and troubleshoot bioanalytical methods
• Present results and findings at internal multidisciplinary project/clinical teams

Profile

• Master's degree or equivalent experience in life sciences
• Experience managing Contract Research Organizations (CROs) is an asset
• Good knowledge of bioanalytical techniques, especially in biologics and antibodies
• Solid understanding of development and validation of bioanalytical assays, including regulatory guidelines (GLP and GCP)
• Hands-on experience with ligand-binding bioanalytical methods such as ELISA, MSD, or Gyrolab is an asset
• Excellent interpersonal skills, team-oriented, and capable of working with external partners
• Strong organizational and communication skills
• Ability to work independently
• Focus on quality
• Proactive, flexible, and adaptable to a fast-growing biotech environment

Offer

We offer a competitive compensation package with extensive benefits. The final level and remuneration depend on experience.

Gain exposure to all aspects of nonclinical and clinical development, working with external vendors, contract partners, and the scientific community.

Enjoy a dynamic, human-sized, rapidly growing biotech company environment.