Senior Regulatory Affairs Associate (Fixed Term Contract) - Remote

TN United Kingdom; Leeds; Remote; GBP 35,000 - 55,000; Full time

Job summary

An established industry player in the pharmaceutical sector is seeking a Senior Regulatory Affairs Associate for a fixed-term remote contract. This role offers a unique opportunity to join a strong regulatory team in Leeds, where you will review market authorisations and contribute to regulatory meetings. The position promises significant development and learning opportunities, making it ideal for someone with GMP experience and a passion for regulatory affairs. If you're looking to advance your career in a supportive environment, this role is perfect for you.

Benefits

Competitive salary

Bonus opportunities

Remote working options

Learning and development opportunities

Qualifications

• Experience in a GMP pharmaceutical environment is essential.
• Strong knowledge of product variations and license maintenance.

Responsibilities

• Review market authorisations and execute variations for submissions.
• Participate in regulatory and cross-functional meetings.
• Maintain regulatory systems and create product information texts.

Skills

Regulatory Affairs

GMP Knowledge

Product Variation

License Maintenance

Education

Degree in Life Sciences

Job description

Senior Regulatory Affairs Associate (Fixed Term Contract) - Remote, Leeds

Join an established Regulatory team in a pharmaceutical company based in Leeds. This role offers great development and learning opportunities.

Client:

Page Personnel

Location:

Leeds, United Kingdom

Job Category:

Customer Service

EU work permit required:

Yes

Job Reference:

bec4b1852ef7

Job Views:

6

Posted:

05.05.2025

Expiry Date:

19.06.2025

Job Description:

1. Review existing market authorisations and execute variations for submissions to authorities.
2. Participate actively within the regulatory team and contribute to regulatory and cross-functional meetings.
3. Maintain regulatory systems.
4. Create and approve product information texts in line with current SOPs and regulatory guidance.

About Our Client

The client is a well-established pharmaceutical developer and manufacturer based in Leeds. They have a strong regulatory function and offer significant learning and development opportunities.

The Successful Applicant

Demonstrable experience within a GMP pharmaceutical environment, with strong knowledge of product variation and license maintenance.

What's on Offer

Competitive salary, bonus, and remote working options.