Internship – Quality Regulatory Engineer MFX

Nemera

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profile Job Location:

Lyon - France

profile Monthly Salary: Not Disclosed
Posted on: 17 hours ago
Vacancies: 1 Vacancy

Job Summary

Location: Nemera Lyon Gerland Site
Field: Medical Devices
Duration: 6 months

 

Join Nemera a global leader in medical device solutions and take part in a strategic project focused on a vaginal applicator produced at our Jaguariúna (Brazil) site.
Within the Parenteral & ICO unit you will support the Quality department in building key regulatory and technical documentation for this device.

 

Your Mission

Working closely with design regulatory laboratory and project teams you will:

  • Develop and structure the Design History File risk management file and Technical File for the product.

  • Ensure proper traceability of project requirements and documentation coordinating with all project stakeholders.

  • Lead and support risk management activities.

  • Challenge and assist the design team throughout their activities.

  • Provide regular activity updates to the Quality Project Manager.


Qualifications :

Your Profile

  • You are currently pursuing a Masters degree (1st or 2nd year) in regulatory quality within the pharmaceutical device field.

  • Strong communication skills.

  • Excellent organizational abilities and attention to detail.

  • Enjoy working in a multicultural cross-functional team (regulatory design lab materials project management etc.).

  • Motivated autonomous and proactive.

  • Very good level of English (spoken and written).

  • Mandatory: Knowledge of ISO 13485.

 

Why Joining Us

  • Contribute to a project with high regulatory and technical impact in the medical device industry.

  • Gain experience within a dynamic international environment.

  • Strengthen key skills in quality risk management and project documentation.


Additional Information :

Our Recruitment Process

We believe in a transparent and straightforward recruitment process to ensure a great fit for both you and our team.
Heres what you can expect:
CV Review: Upon receiving your CV our Talent Acquisition Team will review it to assess your qualifications for the role.
Initial Screening: If your profile matches our requirements youll be invited for an initial screening call with a member of our Talent Acquisition Team.
Interview with Hiring Manager: After the initial screening youll have an interview with the Hiring Manager to discuss your experience skills and fit for the role in more detail.
Offer: If all goes well youll receive an offer to join our team!

We look forward to receiving your application (resume submitted in English is appreciated). We offer varied jobs job in an international group if you want to discover more about Nemera please look at our website

Know someone at Nemera We have a Referral Program so be sure to have them submit you as a referral prior to applying for this position!

Chez Nemera nous valorisons la diversité et linclusion et nous nous engageons à créer un environnement de travail où tous les employés sont traités avec dignité et respect.
Nous sommes fiers dêtre un employeur offrant légalité des chances et nous encourageons les candidatures de toutes les origines genres orientations sexuelles âges et capacités.


Remote Work :

No


Employment Type :

Full-time

Location: Nemera Lyon Gerland SiteField: Medical DevicesDuration: 6 months Join Nemera a global leader in medical device solutions and take part in a strategic project focused on a vaginal applicator produced at our Jaguariúna (Brazil) site.Within the Parenteral & ICO unit you will support the Qual...
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About Company

Nemera Szczecin Sp. z o.o. to  członek światowej grupy Nemera, lidera w produkcji urządzeń do dostarczania leków. Nasze oddziały znajdują się we Francji, Stanach Zjednoczonych, Niemczech i Brazylii. W Szczecinie jesteśmy specjalistami w produkcji wysokiej jakości wstrzykiwaczy do poda ... View more

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