This is a fully remote position, open to applicants in Armenia.

📋 Description

• Preparation of PMCF, CER, CEP, PMS.

• Review of pertinent documents.

• Consultation and gap analysis regarding the transition from MDD to MDR.

• Addressing inquiries from regulatory authorities.

• Conduct literature searches.

• Evaluate data obtained from literature searches.

• Capability to interpret, assess, and translate findings from medical research.

⛳️ Requirements

• Bachelor's degree in Life Sciences.

• Minimum of 4-5 years of experience in medical writing.

• Experience with medical device-related documentation (CEP/CER/PMCF/PSP).

• Proficient in English.

• Knowledge of the French language is advantageous.

• Experience with FDA submissions for medical devices is a plus.

• Regulatory consultation experience is a plus.

🏝️ Benefits

• 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.