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Biotech jobs in United Kingdom

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Milton Keynes
Remote
GBP 60,000 - 90,000
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Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Cheltenham
Remote
GBP 70,000 - 90,000

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Watford
Remote
GBP 80,000 - 120,000

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Bolton
GBP 70,000 - 100,000

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Stoke-on-Trent
Remote
GBP 70,000 - 120,000
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Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Wakefield
Remote
GBP 70,000 - 100,000

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Southampton
Remote
GBP 70,000 - 110,000

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Slough
Remote
GBP 70,000 - 100,000
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Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Birmingham
Remote
GBP 70,000 - 100,000

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Coventry
Remote
GBP 65,000 - 100,000

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Hemel Hempstead
Remote
GBP 70,000 - 100,000

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Hounslow
Remote
GBP 70,000 - 100,000

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Shrewsbury
Remote
GBP 70,000 - 100,000

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Bournemouth
Remote
GBP 80,000 - 120,000

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Guildford
Remote
GBP 70,000 - 110,000

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Wolverhampton
Remote
GBP 70,000 - 120,000

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Basingstoke
Remote
GBP 70,000 - 110,000

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Peterborough
Remote
GBP 70,000 - 100,000

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Woking
Remote
GBP 70,000 - 110,000

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Luton
Remote
GBP 70,000 - 120,000

SOC 2 Type II Specialist

SOC 2 Type II Specialist
JR United Kingdom
Portsmouth
Remote
GBP 80,000 - 100,000

SOC 2 Type II Specialist

SOC 2 Type II Specialist
JR United Kingdom
Wakefield
Remote
GBP 75,000 - 80,000

Global Regulatory Lead

Global Regulatory Lead
JR United Kingdom
Leicester
Remote
GBP 75,000 - 115,000

Principal Talent Partner - 6 Month FTC

Principal Talent Partner - 6 Month FTC
JR United Kingdom
Bath
GBP 40,000 - 60,000

SOC 2 Type II Specialist

SOC 2 Type II Specialist
JR United Kingdom
Milton Keynes
Remote
GBP 75,000 - 80,000

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Global Regulatory Lead

JR United Kingdom
Milton Keynes
Remote
GBP 60,000 - 90,000
Job description

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Freyr is a fast-growing, innovative company specializing in providing end-to-end regulatory solutions and services for the Life Sciences industry. With a commitment to excellence and innovation, we assist pharmaceutical, medical device, and biotech companies in navigating the complexities of regulatory compliance.

Why Freyr?

At Freyr, we believe in fostering a collaborative and dynamic work environment that empowers our team to make a real impact. As we expand our footprint, we are looking for passionate and skilled Regulatory professionals to join us in shaping the future of regulatory services.

Join Our Team:

If you're ready to embark on a journey of growth and innovation, connect with us to explore the exciting opportunities awaiting you at Freyr. Together, we can shape the future of regulatory solutions.

How to Apply:

Please apply to this job post or visit our Careers page for more openings.

Visit our Careers page at https://www.freyrsolutions.com/careers/current-positions to explore current job openings and submit your application.

Don't miss this chance to be part of Freyr's expansion and make your mark in the world of regulatory services. Let's redefine regulatory excellence together!

Position: Global Regulatory Lead / Associate Director - Regulatory Affairs

Location: Remote (Base location should be in UK/EU, preferably in Hungary, Poland, Romania, Czech Republic, or Croatia)

Experience: Minimum 8 years of direct experience with Medicinal Product Regulatory Affairs

Role Summary
  • Serve as a global regulatory liaison (GRL) for select products.
  • Lead a global team of regulatory professionals covering the product (directly and/or indirectly).
  • Chair Regulatory Project Team (RPT) meetings with team and affiliates, as applicable.
  • Collaborate closely with related product GRLs or pediatric/adult GRL counterparts as necessary.
  • Define and execute worldwide RA strategy for the product, providing leadership to align with client’s objectives.
  • Leverage regional/in-country RA team experience to guide global development strategies, risk mitigation, and innovative approaches.
  • Build and maintain partnerships with key stakeholders across RA and cross-functionally.
Key Activities

Strategic activities include:

  • Providing global regulatory leadership for filings, health authority meetings, and internal governance.
  • Representing Regulatory Affairs at key cross-functional meetings such as GDT.
  • Ensuring global strategic alignment and execution across regions.
Experience and Skillset

You will act as the Global Regulatory Liaison for complex products or projects, managing multiple simultaneously. Responsibilities include defining regulatory strategies, managing submissions, and leading cross-functional teams.

  • Contribute to the development of regulatory processes, standards, and efficiencies.
  • Represent Regulatory Affairs on cross-regional teams, providing strategic guidance.
  • Define regulatory strategies for multiple products in development.
  • Identify and mitigate regulatory risks proactively.
  • Oversee regulatory submissions, labeling, and documentation updates.
  • Provide leadership and management to project teams.
  • Ensure compliance with all relevant policies and regulations.
Requirements

Education & Experience:

  • PharmD/PhD with 2+ years relevant experience.
  • MA/MS/MBA with 8+ years relevant experience.
  • BA/BS with 10+ years relevant experience.
  • Extensive regulatory, quality, or compliance experience in biopharma.
  • Proven track record in regulatory strategy and negotiations with authorities.
  • Experience in clinical trials or drug development projects.
  • Leadership experience in managing teams or matrix environments.
  • Experience in therapeutic areas and post-marketing activities preferred.
Additional Qualifications

Degree in life sciences or related field with significant regulatory experience. Proven ability to lead regulatory activities and set strategies for biopharmaceutical products.

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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.

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