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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in assay development, validation, and implementation of qPCR, dPCR, and NGS technologies within a regulated environment. Strong analytical and problem-solving skills are essential for interpreting data and presenting scientific findings effectively.
Highest-signal resume keywords
Assay DevelopmentQPCR TechnologyDPCR TechnologyNGS TechnologyRegulated Environment Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Molecular GeneticsGenomics TechnologiesData AnalysisTroubleshootingTechnical Report WritingProtocol DevelopmentLaboratory Studies ManagementQuality ComplianceDesign Control ProceduresRNA and DNA Technologies
Soft Skills
Problem-SolvingDecision-MakingOrganizational SkillsCollaborationCommunication
Tools & Technologies
Microsoft OfficeExcelPowerPointWord
Industry Keywords
ISO 13485Clinical TrialsLaboratory ActivitiesTechnical DocumentationCross-Functional Collaboration
About the role
Key responsibilities & impact- Manage, plan, and execute complex technical and laboratory studies
- Write protocols and review and approve documentation in accordance with design control procedures
- Perform laboratory activities supporting assay development, validation, and implementation across multiple workflows
- Troubleshoot, interpret, and analyze data
- Evaluate and document studies and present results in technical reports
- Collaborate with internal teams and cross-functional stakeholders to deliver projects safely, efficiently, and in compliance with quality and regulatory requirements
- Prepare and present scientific data for internal and external projects
- Organize, lead, and participate in departmental and client meetings
- Develop, validate, and implement qPCR, dPCR, and NGS assays for clinical trials using RNA and DNA technologies
Requirements
What you’ll need- Master’s degree or PhD in Life Sciences or an equivalent discipline
- Minimum of 3 years of relevant experience in assay development or a related role within a highly regulated environment
- Strong foundation in molecular genetics and genomics technologies
- Hands-on experience in assay development using qPCR, dPCR, and/or NGS technologies
- Experience working in a regulated environment (ISO 13485) is considered an asset
- Proficiency with Microsoft Office applications, particularly Excel, PowerPoint, and Word
- Excellent problem-solving and decision-making skills
- Results-oriented, analytical, and creative thinker with a proactive approach
- Strong organizational skills with the ability to manage multiple priorities and projects simultaneously
- High level of accountability and attention to detail
- Strong troubleshooting, data analysis, and interpretation skills
- Collaborative, adaptable, and diplomatic team player with excellent communication and interpersonal skills
- Fluent in English, both written and spoken
- Demonstrated eagerness to learn and apply new concepts and technologies
- Legally authorized to work in Belgium
Benefits
Comp & perks- Hybrid work schedule
- Full-time employment
- Work with state-of-the-art RNA and DNA technologies
- Opportunity to contribute to innovative genomic assays supporting clinical trials
- Work with dedicated professionals focused on impacting patient therapy