Regulatory Affairs Manager Apply now
Regulatory Affairs Manager

Regulatory Affairs Manager

Maidenhead Full-Time 43200 - 72000 £ / year (est.)
Apply now
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At a Glance

  • Tasks: Lead post-approval compliance and support pre-approval activities in a dynamic environment.
  • Company: Join a growing generic pharmaceutical company with an extensive portfolio of 220 licenses.
  • Benefits: Enjoy competitive salary, career growth opportunities, and a collaborative work culture.
  • Why this job: Be part of a team making a real impact in the pharmaceutical industry while advancing your career.
  • Qualifications: Must have experience in regulatory affairs and a strong understanding of compliance processes.
  • Other info: This role offers a chance to shape the future of healthcare through innovative solutions.

The predicted salary is between 43200 - 72000 £ per year.

An exciting opportunity for an experienced Regulatory Affairs Manager to take on a new role in a growing generic pharmaceutical company working towards a portfolio of 220 licenses.

Responsibilities:

  • Primarily responsible for post-approval and compliance activities with a support role for the pre-approval team
  • Have an excellent understanding of and be able to execute activities related to the followin…

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Regulatory Affairs Manager employer: Select OH

Join a dynamic and innovative team at our growing generic pharmaceutical company, where your expertise as a Regulatory Affairs Manager will be valued and impactful. We offer a collaborative work culture that fosters professional growth and development, along with competitive benefits that support your well-being. Located in a vibrant area, our company provides unique opportunities to contribute to a diverse portfolio of 220 licenses, making your role both meaningful and rewarding.
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Contact Detail:

Select OH Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Regulatory Affairs Manager

✨Tip Number 1

Make sure to familiarize yourself with the specific regulations and compliance requirements in the pharmaceutical industry. This knowledge will not only help you during the interview but also demonstrate your commitment to the role.

✨Tip Number 2

Network with professionals in the regulatory affairs field. Attend industry conferences or webinars to connect with others who may have insights into the company or the role you're applying for.

✨Tip Number 3

Prepare to discuss your previous experiences in post-approval and compliance activities. Be ready to share specific examples of how you've successfully navigated challenges in these areas.

✨Tip Number 4

Research the company's portfolio and recent developments in their product licenses. Showing that you are informed about their work will set you apart as a candidate who is genuinely interested in contributing to their success.

We think you need these skills to ace Regulatory Affairs Manager

Regulatory Knowledge
Post-Approval Compliance
Pharmaceutical Industry Experience
Attention to Detail
Project Management
Communication Skills
Problem-Solving Skills
Team Collaboration
Analytical Skills
Knowledge of FDA and EMA Regulations
Risk Assessment
Documentation Skills
Time Management
Adaptability

Some tips for your application 🫡

Understand the Role: Make sure to thoroughly read the job description for the Regulatory Affairs Manager position. Highlight the key responsibilities and required skills, and think about how your experience aligns with these.

Tailor Your CV: Customize your CV to emphasize your relevant experience in regulatory affairs, particularly in post-approval and compliance activities. Use specific examples that demonstrate your expertise in managing licenses and compliance.

Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your enthusiasm for the role and the company. Mention your understanding of the pharmaceutical industry and how you can contribute to their portfolio of licenses.

Proofread Your Application: Before submitting, carefully proofread your application materials. Check for any grammatical errors or typos, as attention to detail is crucial in regulatory affairs.

How to prepare for a job interview at Select OH

✨Understand Regulatory Frameworks

Make sure you have a solid grasp of the regulatory frameworks relevant to the pharmaceutical industry. Be prepared to discuss how these regulations impact post-approval and compliance activities.

✨Showcase Your Experience

Highlight your previous experience in regulatory affairs, especially any roles that involved managing post-approval processes. Use specific examples to demonstrate your expertise and problem-solving skills.

✨Prepare for Compliance Questions

Expect questions related to compliance activities. Be ready to explain how you ensure adherence to regulations and how you handle compliance issues when they arise.

✨Demonstrate Team Collaboration

Since the role involves supporting the pre-approval team, emphasize your ability to work collaboratively with cross-functional teams. Share examples of how you've successfully partnered with others to achieve regulatory goals.

Regulatory Affairs Manager
Select OH Apply now
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  • Regulatory Affairs Manager

    Maidenhead
    Full-Time
    43200 - 72000 £ / year (est.)
    Apply now

    Application deadline: 2027-01-07

  • S

    Select OH

  • Other open positions at Select OH

    S
    Deputy Regulatory Manager

    Select OH

    Maidenhead Full-Time
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