Regulatory Affairs Manager M CDI H/F - 69

With sales of €500m and 2,800 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.We are currently looking for passionate people ready to make a difference in the following open position: Regulatory Affairs Manager F/M/X, based in Lyon (7e).

Within Nemera's headquarters, you will lead the Regulatory & Compliance design projects of drug delivery devices for one of our strategic products BU.

You will report to the Quality and Regulatory Management of the BU. You will work closely with the development team, from requirements through to architecture, development, industrialisation, quality, covering all aspects from defining regulatory strategy, and supporting quality management plans through to QMS development and process improvement.

Job Description :

- You will manage the Regulatory & Compliance team of the Business Units Parenteral/Biologics/Intimate Care and Oral.
- You will be in charge of the resources assessment needed for regulatory and normative activities under your ownership and product platform.
- You will collaborate with Regulatory and Compliance Project Managers in building the product regulatory strategy and regulatory impact assessment of changes, linked to the device part and combination products.
- You will collaborate with development teams and with the production site(s) to ensure correct implementation of regulatory and normative activities of the products and concerned production sites.
- You will support and guide our customers in their notification procedure particularly in EU, US and Canada.
- You will collaborate with different teams to contribute to the continuous improvement processes.
- You will support the Regulatory Team in the preparation, verification and approval, of regulatory documents and collect normative information needed for the submission to the authorities, notified body or customers.
- Contribute and assist when necessary to internal or external audits and propose corrective and preventive actions.
- You will collect and interpret elements of the monitored standards, inform product or process managers for the changes, analyze and synthesize gaps and collaborate with other departments of the company to guarantee normative compliance.
- Support development teams during product-specific normative interactions with external stakeholders, such as regulatory organisms and customers.
- You may participate in standardization committees and external expert groups in order to understand, anticipate and influence existing or new standards.
- You will conduct in-depth analyzes of proposed product changes, assessing their impact, evaluating the normative compliance and proposing corrective measures if necessary
- Collaborate closely with other BUs

If you are:

· Passionate about growing a business
· Enjoy working as a team
· Proud to make products that improve patients' lives
· And go the extra mile to deliver on your commitments,

Then you'll be successful here!