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Our client is a well-established chemical organization based in the Northwest region, currently seeking an experienced QA/Regulatory Affairs professional with several years of experience, ideally within the chemical sector.
The successful candidate will hold a degree in chemistry or a related discipline and have 3-5 years of experience working in an ISO 9001:2015 quality environment.
Principal Responsibilities
- To prepare and maintain regulatory documents for submission to regulatory authorities, including collecting, reviewing, and managing manufacturing and other supporting documentation.
- To collaborate with regulatory authorities and counterparts to ensure compliance and effective communication.
- To stay up to date with legislation related to the manufacture, labelling, transport, and supply of products to ensure full compliance.
- To have experience in areas such as REACH, CLP, Safety Data Sheets, and Dangerous Goods Notes (DGNs).
- To handle submissions for independent approvals from organizations like WRAS, KIWA, DVGW, and similar entities.
Required Skills and Abilities
The Senior QA/Regulatory Affairs Scientist should demonstrate the following:
- Ability to work independently and manage tasks effectively under pressure.
- Strong skills in conveying technical concepts both verbally and in writing.
- Capability to engage with clients on technical matters.
- Excellent attention to detail and the ability to handle multiple tasks simultaneously.
- Solid numeric skills and computer literacy.
- Enthusiasm and aptitude for identifying and solving problems.
All applicants must be living in the UK and be eligible to work.
