Deadline:
As soon as possible
Location(s)
France
63 Avenue Tony Garnier, Lyon, Auvergne-Rhône-Alpes
Overview
Details
Company Description
With sales of €600m and 3000 employees worldwide, Nemera is one of the leading global manufacturers of complex drug delivery systems for the pharmaceutical industry, offering to patients a broad product portfolio which includes inhalation devices, injection devices, nasal and dermal pumps and ophthalmic delivery devices. Nemera has built very long lasting, strong relationships with the leading global pharmaceutical companies globally by providing high quality development, industrialization and manufacturing services. Nemera develops and manufactures its own IP product platforms but also offers also fully custom developments and contract manufacturing.
Nemera’s manufacturing sites are located in the US, France, Germany, Brazil and Poland. The headquarters and Innovation Center for early device design and development are located in France (Lyon).
We have big ambitions at Nemera! We are growing our franchises and strengthening our capabilities.
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.
Opportunity is About
Eligibility
Candidates should be from:
Description of Ideal Candidate
Your Profile
-
You are currently pursuing a Master’s 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.
Dates
Deadline: As soon as possible
Cost/funding for participants
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.
Un-save Opportunity
Internships, scholarships, student conferences and competitions.
