Regulatory Manager Reach

il y a 7 jours

Lyon, France Staphyt Temps plein

We strengthen science together

Present in Europe, North Africa, South America, STAPHYT brings together more than 600 employees, of different nationalities and cultures.

Rich in multiple profiles, a wide range of expertise is expressed in the Group, through our areas of activity which are agronomic experimentation, regulatory advice and coordination of registration files.

In a situation of non-stop growing demand, we’re working to build the best teams by inspiring, challenging and hiring the brightest talents from all over the World.

Staphyt’s Regulatory Affairs Division supports its clients in successfully bringing substances and products to the market. We help clients understand and address the regulatory requirements for chemical or biological active substances and products in Biocides, REACH, Plant Protection & Nutrition sectors. Skills, experience and geographical coverage are three essential assets of our team to enable our clients to achieve their regulatory affairs objectives.

**Tasks**:
We are currently looking for an enthusiastic and motivated Regulatory Manager to join our expanding Reach & Biocides Teams in Europe.

The purpose of this role is to deliver high quality and cost effective services to clients, by providing regulatory consultancy and delivering the client’s regulatory objectives through efficient project management.

You will work closely alongside our wider Regulatory & Scientific Teams, and directly with the client’s team. A joined up and consistent approach is needed across all areas of expertise, so proactive communication and strong team working skills are essential.

**Main duties**:

- Data Gap Analysis (DGA) including early phase testing strategy for active substance and/or product dossiers
- Preparation and submission of REACh (joint and lead) and BPR dossiers (under IUCLID format)
- PCN submissions and SDS revision and other related product safety compliances
- Regulatory watch support and preparation
- Application of national registrations under transitional period arrangements
- Providing strategic advice to clients and representing them in communication with Regulatory Authorities
- Various other tasks related to the registration of substances and products in Europe and the UK

**Your profile**:
**Skills and experience required**:
**Essential**:

- Relevant scientific degree
- Ability to understand and accurately interpret regulatory requirements in order to make appropriate scientific and regulatory conclusions, provide advice and strategy to clients
- Standard knowledge of CLP, REACh and Biocides (BPR) regulation, and processes
- Evidence of ability to build and maintain strong and professional relationships with prospective and existing clients
- Good command of key tools (IUCLID, R4BP3)
- Strategic awareness
- Team player with strong decision-making skills, keen to be part of a geographically dispersed team and to work in an international business environment
- Ability to work independently
- Have a good attention to detail
- Be a good communicator
- Excellent written and verbal communication skills in English

**Desirable**:

- At least 2 years experience in Reach and/or Biocides sector of the EU/UK regulatory regime, preferably gained within industry and/or consultancy
- Knowledge of regulatory frameworks in other jurisdictions (GB BPR, EMEA, LATAM ) or other sectors (REACH, detergents, cosmetics, medical devices, pharmaceuticals,)

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