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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in laboratory analyses and testing within Quality Control, with a strong focus on analytical methods such as ELISA, Immunoblot, and qRT-PCR. Proficient in GMP compliance, data traceability, and effective collaboration in multidisciplinary teams.
Highest-signal resume keywords
ELISAImmunoblot / Western BlotQRT-PCR / qPCRGMP / GxP KnowledgeAnalytical Method Validation
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Laboratory AnalysisAnalytical Method ImplementationData VerificationAnalytical Protocol ExecutionCoagulation Assays
Soft Skills
Strong Organizational SkillsAutonomyCollaboration
Industry Keywords
Quality ControlPharmaceuticalBiotechnologyRegulated EnvironmentAnalytical Investigations
About the role
Key responsibilities & impact- Perform laboratory analyses and testing within QC.
- Implement analytical methods including ELISA, Immunoblot / Western Blot, and qRT-PCR / qPCR.
- Participate in the implementation and qualification of new analytical methods on coagulation equipment.
- Participate in drafting and implementing method protocols.
- Analyze, verify, and review analytical results.
- Contribute to investigations of atypical results, deviations, or nonconformities.
- Ensure data traceability and document compliance in accordance with GMP requirements.
- Collaborate with QC, Quality Assurance, Analytical Development, and other project functions.
- Participate in analytical method transfer and lifecycle activities.
Requirements
What you’ll need- Educational background as a laboratory technician, biomedical analysis technician, biologist, biochemist, biotechnologist, or equivalent.
- Initial experience, ideally in a pharmaceutical or biotechnology QC laboratory or another highly regulated environment.
- Hands-on experience with ELISA.
- Experience with Immunoblot / Western Blot.
- Experience with qRT-PCR / qPCR.
- Strong command of laboratory practices and related documentation.
- Knowledge of GMP / GxP environments.
- Ability to execute analytical protocols and interpret results.
- Thoroughness, autonomy, and strong organizational skills.
- Ability to work effectively in multidisciplinary teams.
- Fluent French.
- Professional working proficiency in English.
- Experience in analytical method validation or transfer, coagulation assays, release testing and/or stability testing, analytical investigations, deviations and CAPA, as well as experience in a pharmaceutical QC environment, would be an additional advantage.
Benefits
Comp & perks- Personalized support for your professional development.
- Innovative, high-value industrial projects.
- An entrepreneurial environment that encourages initiative.
- The opportunity to become a shareholder in the group.
- A strong commitment to innovation, CSR, and employee development.
- Dedicated policies supporting parenthood and work-life balance.
- All our positions are open to people with disabilities, regardless of gender, background, or sexual orientation.