Medical device technical expert - Contraceptives

TN France; France; À distance; EUR 50 000 - 80 000; Plein temps

Résumé du poste

An established industry player is seeking a Medical Device Technical Specialist with expertise in contraceptives. This home-based role offers the chance to impact patient safety through technical reviews and client support. Ideal candidates should possess a relevant degree and extensive experience in medical device development. Join a collaborative and client-centric team dedicated to quality and innovation in the medical field. This position includes opportunities for travel and professional growth, making it perfect for those looking to advance their careers in a meaningful way.

Qualifications

• 5+ years of experience in designing and developing contraceptive medical devices.
• Knowledge of medical device regulations and certification processes.

Responsabilités

• Deliver Medical Device CE Marking technical reviews under MDD and MDR requirements.
• Provide advice and support on certifications in your area of expertise.

Connaissances

Analytical Skills

Communication Skills

Diligence

Curiosity

Knowledge of Medical Device Regulations

Formation

Bachelor's degree or higher in a relevant discipline

Description du poste

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Medical device technical expert - Contraceptives, France

Client: BSI

Location: France

Job Category: -

EU work permit required: Yes

Job Reference: 6fd700e5cf67

Job Views: 1

Posted: 06.05.2025

Expiry Date: 20.06.2025

Job Description:

Great that you're considering a career with BSI!

Are you excited to grow your career? Our people make all the difference in our success.

BSI is a designated European Notified Body, an accredited ISO 13485-certification body, a recognized Auditing Organization under MDSAP, and we have an opportunity for you to join our growing team!

We are seeking a Medical Device Technical Specialist with contraceptives expertise, including condoms and lubricant gel-related medical devices.

Our Technical Specialists are industry experts who are analytical, communicative, diligent, and curious. If you're looking for a career change and want to impact patient safety – this could be a great fit! This is a home-based position with up to 25% travel (when COVID-19 travel restrictions lift).

Your responsibilities include:

1. Deliver Medical Device CE Marking technical reviews under MDD and MDR requirements, scheme management, and ISO 13485 QMS assessment services.
2. Provide advice and support on certifications in your area of expertise, especially where regulatory challenges arise.
3. Participate in client meetings to facilitate CE marking processes.
4. Provide leadership and mentoring in medical device expertise to personnel.
5. Support technical sales and networking activities as needed.

Ideal candidate characteristics:

• Bachelor's degree or higher in a relevant discipline or equivalent qualification.
• At least five (5) years of post-graduate experience in designing and developing contraceptive medical devices/products, including principles of design control, risk management, and clinical evaluation.
• Knowledge of medical device regulations.
• Awareness of certification processes, quality management standards, and audits.

Advantages:

• Exposure to clinical, risk management, biological safety, and validation processes.

Our core behaviors are Client-centric, Agile, and Collaborative, guiding how we work at BSI to ensure a positive environment and business success.

We conduct face-to-face interviews where appropriate. If invited but more comfortable interviewing virtually, please discuss this with our recruitment team.