Main characteristics
- Location
- Kent
- Company
- Cranleigh Scientific
- Salary
- £55000 - £65000/annum
- Employment type
- Permanent
- Category
- Medical / Pharmaceutical / Scientific
Job summary
We have an exciting opportunity for a Regulatory Affairs Manager to join our pharmaceutical client. You will play a crucial role in responding to customer queries regarding regulatory issues concerning company products, particularly in the pharmaceutical and supplement sectors. You must have proven leadership experience along with significant regulatory experience in the pharma and/or food markets. This is a permanent role offering flexible working hours.Job Overview:
We are searching for a dynamic and experienced Regulatory Affairs Manager to lead a Regulatory Affairs (RA) team. The main duty of this position is to oversee the RA team and guarantee the provision of regulatory support to customers regarding company products and services. The Regulatory Affairs Manager will have a vital role in addressing customer inquiries related to regulatory issues in the pharmaceutical and supplement sectors. Moreover, the role includes interacting with industry associations and Regulatory Authorities, keeping the business informed about the latest relevant regulatory information in collaboration with the Regional Regulatory Director.
Key Responsibilities:
Manage and lead the Regulatory Affairs team to ensure effective provision of regulatory support.
Respond to customer queries related to regulatory issues concerning Company products in the pharmaceutical and supplement sectors.
Engage with industry associations and Regulatory Authorities as required.
Update the business with the latest regulatory information in collaboration with the Regional Regulatory Director.
Ensure compliance with regulatory requirements and standards.
Work closely with cross-functional teams to integrate regulatory considerations into business strategies.
Provide leadership and guidance on regulatory matters to internal teams.Qualifications and Experience:
A relevant scientific degree or equivalent experience in quality, regulatory, or manufacturing.
Leadership experience, inclusive of training, mentoring and/or managing.
Experience within the pharmaceutical, excipient, or food industries in a regulatory role
Familiarity with regulatory requirements in the pharmaceutical and supplement sectors.
Proven ability to work to deadlines and manage a well-organized approach to the workload.
Strong communication and interpersonal skills.
Self-motivated with the ability to work independently and lead a small team.
Must be proficient in MS Office
Technical writing and proofreading skills
Excellent Communication Skills at all levels of organisation.
Fluent English (additional languages would be beneficial)
This is a 37.5 hour working week, offering flexible working hours
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