Associate Assay Development Scientist (Histopathology)

CellCarta; Antwerpen; Hybride; EUR 42 000 - 65 000; Plein temps

Avantages offerts par ce poste

CellCarta Days

Meal vouchers

Insurance

Bike leasing

Public transport reimbursement

Career advancement opportunities

Résumé du poste

CellCarta Belgium invites applications for an Associate Assay Development Scientist in Histopathology. You will assist the Assay Development Unit in optimizing and validating IHC, RISH, FISH, and CTC assays for clinical trials, collaborating with QA, RA, and Clinical Sample Testing teams.

The role emphasizes project coordination, data analysis, and report preparation, with a strong focus on documentation, quality, and regulatory compliance.

Qualifications

• Master's degree in Life Sciences (Biology, Biomedical Sciences, Bioengineering, Pharmaceutical Sciences, or Biochemistry preferred).
• Basic knowledge of histology and automated immunohistochemical techniques.
• Strong English, writing and communication skills.
• Excellent organizational skills and attention to detail.
• Ability to learn quickly and adapt to new areas.

Responsabilités

• Assist the Assay Development team through all project phases including start-up, design, scheduling, and reporting.
• Coordinate transition of experiments to the lab and support laboratory execution.
• Maintain proactive communication with internal stakeholders to ensure transparency.
• Provide updates and collaborate to meet project objectives.
• Ensure compliance with quality and regulatory standards for intended use.

Connaissances

Written & verbal communication

Analytical thinking

Project coordination

Time management

Formation

Master's degree in Life Sciences

Outils

Microsoft Excel

PowerPoint

Word

Description du poste

Associate Assay Development Scientist - Histopathology

Are you looking to make your next career move? CellCarta, a CRO, is hiring an Associate Assay Development Scientist to join our dynamic team. As an Associate Assay Development Scientist, you will have the opportunity to use your expertise and skills to ensure that our services meet the highest industry standards. Come work with a team of talented individuals who are committed to making a positive impact on human health and well-being.

Position Summary

The Assay Development Unit is responsible for the optimization and validation of high-quality (single and multiplex) IHC, RISH, FISH, and CTC assays for use in clinical trials. As an Associate Assay Development Scientist, you will collaborate with the Assay Development team and other internal stakeholders (such as Laboratory Operations, QA, RA, and the Clinical Sample Testing Unit) throughout all stages of the development and validation process.

Key Responsibilities

• Assist the Assay Development team throughout all phases of a project, including start-up, experimental design, scheduling, tracking development and validation activities, evaluating immunohistochemically stained images, data analysis, and report preparation
• Coordinate the smooth transition of scheduled experiments to the laboratory. While this role does not include hands‑on experimental work, it plays a key role in supporting laboratory execution
• Engage proactively with internal stakeholders to ensure clear, timely, and transparent communication
• Anticipate potential issues, provide regular updates, and collaborate effectively to meet project‑specific objectives
• Ensure compliance with relevant quality and regulatory standards for the intended use

Qualifications

Required Qualifications

• Master's degree in Life Sciences (preferably Biology, Biomedical Sciences, Bioengineering, Pharmaceutical Sciences, or Biochemistry)
• Basic knowledge of histology and automated immunohistochemical techniques
• Strong computer skills and proficiency in Microsoft Excel, PowerPoint, and Word
• Advanced command of the English language, along with outstanding writing and communication skills
• Ability to rapidly learn and apply knowledge in previously unfamiliar areas
• Excellent organizational skills, including time management, attention to detail, and the ability to prioritize tasks efficiently
• Demonstrates a high quality of work, including accuracy, timeliness, professionalism, and thoroughness
• Analytical, problem‑solving, and results‑oriented mindset
• Strong interpersonal skills, diplomacy, a collaborative mindset, and effective communication skills

Preferred Qualifications

• Strong background in histology, histopathology, and/or microscopy

Work Arrangements

• Full‑time position (38 hours per week), Monday to Friday, 9:00 a.m. to 5:00 p.m., with a hybrid work arrangement requiring 2‑3 days of onsite attendance per week
• Location:Sint-Bavostraat 78, 2610 Antwerpen (Wilrijk), Belgium

Benefits

• Competitive salary
• 9 additional CellCarta Days (prorated based on full‑time or part‑time status)
• Meal vouchers (€8 per working day)
• Net allowance
• DKV hospitalization insurance
• Group insurance plan with employer contributions
• Bike leasing after six months of service
• Public transportation reimbursement or bicycle/car allowance
• Career advancement opportunities

About CellCarta

CellCartais a global CRO that provides muti‑omic pharma laboratory services though a harmonized global footprint and integrated logistics, spanning translational research through late phase clinical trials. At CellCarta, science is not just a discipline, but also a shared purpose. We’re a global team of experts across eight facilities in five countries, united by a commitment to propel precision medicine and make a difference in the lives of patients around the world!

Joining CellCarta means working with a team of dedicated professionals who are focused on achieving our mission to solve the scientific and operational barriers that hold back complex clinical programs, while being supported by a collaborative environment where expertise, curiosity, and contributions truly matter.

Map out your future with us!