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About the role
Key responsibilities & impact- Preparation of PMCF, CER, CEP, PMS.
- Review of relevant documents.
- Consultation and gap analysis on transition from MDD to MDR.
- Responses to queries from regulatory authorities.
- Perform literature search.
- Appraise literature search data.
- Ability to interpret, evaluate, and translate medical research findings.
Requirements
What you’ll need- Degree in Life Sciences.
- At least 4-5 years of experience in medical writing.
- Experience in medical device-related documents (CEP/CER/PMCF/PSP).
- Fluent in English.
- Knowledge of French language is a plus.
- Submissions to FDA is a plus (for medical devices).
- Regulatory consultation is a plus.
Benefits
Comp & perks- Why Choose Excelya?
- At Excelya, we lead with Audacity, act with Care, and move with Energy. We nurture your potential through high-impact projects, give your talents the space to shine, and push boundaries to elevate every patient’s journey. Here, you're not just doing a job—you’re becoming a key part of something bigger.
- So, if you're ready to excel with purpose, let’s write the next chapter together
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
medical writingPMCFCERCEPPMSliterature searchdata appraisalregulatory submissionsregulatory consultationmedical research interpretation
Soft Skills
communicationconsultationgap analysisevaluationtranslation