Remote CMC Regulatory Affairs Consultant (Vaccines) in Harrow

Remote CMC Regulatory Affairs Consultant (Vaccines) in Harrow

Harrow Full-Time 60000 - 80000 Β£ / year (est.) No working from home possible
Meeveem Limited

At a Glance

  • Tasks: Develop submission strategies and review regulatory content for vaccines.
  • Company: Join Parexel, a leader in regulatory affairs with a global impact.
  • Benefits: Flexible remote work, competitive salary, and opportunities for professional growth.
  • Other info: Collaborative environment with a focus on innovation and career advancement.
  • Why this job: Make a difference in global health by ensuring vaccine compliance.
  • Qualifications: Experience in regulatory affairs and strong communication skills.

The predicted salary is between 60000 - 80000 Β£ per year.

Parexel is seeking an experienced Regulatory Affairs Consultant to join our European client project.

The role focuses on post-approval CMC activities for vaccines or biologics and can be office or home based across Europe.

You will develop submission strategies, review regulatory content, and coordinate with cross-functional teams to ensure worldwide submissions meet health authority expectations.

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Remote CMC Regulatory Affairs Consultant (Vaccines) in Harrow employer: Meeveem Limited

Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.

Meeveem Limited

Contact Details:

Meeveem Limited Recruitment Team

We think you need these skills to ace Remote CMC Regulatory Affairs Consultant (Vaccines) in Harrow

Regulatory Affairs Expertise
Post-Approval CMC Activities
Submission Strategies Development
Regulatory Content Review
Cross-Functional Team Coordination
Knowledge of Health Authority Expectations
Experience with Vaccines or Biologics