Azelis Group NV · Unavailable
Regulatory Product Manager
HybridMidHertford, the United KingdomApplications closedHealthTech
Our Take
Build compliant solutions for Azelis's Pharmaceuticals & Healthcare business.
What you’ll do
- Manage regulatory enquiries from customers and principals
- Complete regulatory questionnaires
- Support provision of documentation
- Provide regulatory support to SHEQ Manager
- Implement company procedures
- Support SHEQ team audits
- Manage interactions with regulatory authorities
- Review and maintain quality and technical agreements
What they’re looking for
- Knowledge of UK/EU Pharma, Medical Device, Nutraceutical legislation
- Excellent communication and interpersonal skills
- Ability to build relationships with stakeholders
- Ability to work under pressure and manage priorities
- Good IT skills and proficiency with relevant systems
What you get
- Hybrid working flexibility
- Full-time permanent position
Skills & Focus Areas
- regulatory affairs
- pharmaceuticals
- medical devices
- nutraceuticals
- communication
- stakeholder management
- IT skills
As posted by Azelis Group NV
Azelis is seeking a highly motivated individual with strong regulatory expertise covering Pharmaceuticals & Healthcare business unit as a Regulatory Product Manager in the UK. Experience or working knowledge of medical and nutraceutical regulations would be advantageous.
At Azelis, we are committed to delivering innovative and compliant solutions across the Pharmaceuticals & Healthcare sector. As a global leader in the distribution of speciality ingredients and chemicals, we partner with leading suppliers and combine deep industry expertise to support our customers in bringing safe, effective, and high-quality products to market.
Based in Hertford, this full-time permanent position offers the flexibility of hybrid working, enabling you to balance your professional and personal commitments while making a meaningful impact.
Job Purpose
The Regulatory Product Manager will be responsible for managing regulatory enquiries from customers and principals, while also supporting the technical and commercial teams.
Principal Accountabilities
Manage regulatory enquiries from customers and principals.
Complete relevant regulatory questionnaires.
Support the provision of documentation in response to customer enquiries.
Provide regulatory support to the SHEQ Manager.
Implement company procedures as required.
Support SHEQ team audits and manage interactions with regulatory authorities.
Review and maintain quality and technical agreements for customers.
Assist the technical administrator with documentation for the customer portal.
Liaise, where required, with Corporate SHEQ and Regulatory colleagues.
Support Sales and Principal Manager teams with direct customer interactions.
Key Skills & Experience
Knowledge of Pharmaceutical, Medical Device, and Nutraceutical legislation within the UK/EU, or willingness to develop expertise across all areas.
Excellent communication and interpersonal skills.
Strong team player with a collaborative approach.
Ability to build relationships and liaise with stakeholders at all levels, both internally and externally.
Ability to work effectively under pressure and manage competing priorities.
Good IT skills and proficiency with relevant tools and systems.