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Regulatory Affairs Manager – Biocides/Medical Device – Basel
ARM Life Sciences are currently partnered with a business with a global footprint across the scientific organisation with major manufacturing and R&D facilities across the EU and US. Currently they are looking for a Regulatory Affair manager to join their Biocide area of the business in Basel.
Working within a dedicated regulatory affairs team, the successful candidate will support the programme of work required to deliver the regulatory strategy and provide an efficient regulatory and registration service responsive to both internal and external customers. Regulatory experience gained within a Biocides or medical device environment is required.
This is a highly varied role involving coordination, compilation, submission and follow up on EMEA product registration applications. This will be done in close coordination with the EMEA Commercial Team, Technical Team and the Senior Regulatory Assurance Manager for the Biocides area of the business.
In this role supporting internal and external customers is pivotal to the success of the role and this will require you to provide information on product registration as well as general regulatory support and insights.
The successful candidate will have significant industrial experience in a regulatory environment (preferably gained within the biocides sector) as well as the following:
• Post graduate or degree level (or equivalent experience)
•Preferred area of study: ideally Life Sciences or Chemistry based knowledge
• Excellent working knowledge of the EU regulatory framework for biocides or medical device
• Knowledge in REACH, CLP or Plant protection
• Understanding of chemistry, efficacy, toxicology, eco toxicology or environmental fate studies and risk assessment methodologies.
This role is offering a competitive salary plus benefits package. If you are interested in this role please contact Vik Patel at ARM Life Sciences on 00442392 458031 or email me on email@example.com
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