Regulatory Affairs Manager

Regulatory Affairs Manager

Full-Time 36000 - 60000 £ / year (est.) No working from home possible
Astute Healthcare Ltd.

At a Glance

  • Tasks: Lead a national approval team, ensuring smooth operations and effective collaboration.
  • Company: Join a global pharmaceutical company committed to quality and compliance.
  • Benefits: Enjoy competitive pay, health insurance, and career growth opportunities.
  • Other info: Work hours are 8 AM to 5 PM, with a focus on quality assurance.
  • Why this job: Be part of a dynamic team that values open communication and inclusivity.
  • Qualifications: 5+ years in pharma, strong organisational skills, and a relevant degree required.

The predicted salary is between 36000 - 60000 £ per year.

Salary:

Competitive.

Job Timings:

8 AM to 5 PM.

Requirements:

Graduation in pharmacy background or any relevant degree.

About The Role:

  • Supervision and motivation of national approval team members.
  • Contact person for all team members.
  • Proactively ensuring smooth team operations and effective collaboration.

Responsibilities:

  • Creating an inspiring team environment with an open communication culture.
  • To ensure the management of authorized activities and quality records are maintained accurately.
  • CAPA, Deviation, SOP drafting, Training of the team, supplier Audits.
  • Co-ordinating with manufacturers and promptly performing any recall operations.
  • Conducting the suppliers and customer audits as per the procedures.
  • To ensure that the self-inspections are performed at appropriate regular intervals following a prearranged programme and necessary corrective measures are put in place.
  • To ensure and approve final disposition of returned, rejected, recalled or falsified products are dealt
    with effectively.
  • Approve any returns to saleable stock, providing quality support and oversight for Distribution
    Operation review meetings with Distribution contractors.
  • Contribute to defining GDP, quality, KPI’s and OT review quality indicators with recommendations
    for actions for improvement in regard to GDP guidelines.
  • Ensuring CAPA’s are identified, effective temperature control of medicines, temperature mapping.
  • Ensuring annual GDP, initial and continuous training programmes are implemented and maintained
    to all employed staff.
  • Ensure Quality Technical Agreements are in place for all outsourced activities and with all subcontractors.
  • Ensure that the Parallel Import design and relabelling is according to the EU GDP standards
  • Maintaining required documentations and licenses for the processing of these licenses.
  • Extensive experience in the pharmaceutical industry, with a strong background in distribution or quality assurance.
  • Thorough understanding of German and EU regulations pertaining to pharmaceutical distribution including GDP requirements.
  • Excellent organizational skills, with a keen attention to detail and accuracy.
  • Strong interpersonal and communication abilities, with the capacity to collaborate effectively with internal and external stakeholders.
  • Ability to work autonomously, manage multiple priorities, and make informed decisions in a
    dynamic environment.

Candidate Requirements:

  • Minimum 5 years of relevant experience.
  • an analytical and problem-solving mindset.
  • excellent organization and time management skills.
  • commercial or pharmaceutical training.
  • good knowledge of English.
  • confident use of MS Office.
  • ability to work in a team.
  • flexibility and commitment; forward-thinking.

Benefits:

  • Competitive salary and performance-based incentives.
  • Comprehensive benefits package including health insurance.
  • Opportunities for career growth and advancement within a global organization.
  • Dynamic and collaborative work environment with a diverse and inclusive culture.
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Regulatory Affairs Manager employer: Astute Healthcare Ltd.

As a Regulatory Affairs Manager, you will thrive in a dynamic and collaborative work environment that values diversity and inclusivity. Our company offers competitive salaries, performance-based incentives, and a comprehensive benefits package, ensuring that you are well-supported in your role. With ample opportunities for career growth within a global organisation, you will be empowered to develop your skills while contributing to the vital work of ensuring pharmaceutical quality and compliance.

Astute Healthcare Ltd.

Contact Details:

Astute Healthcare Ltd. Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Regulatory Affairs Manager

Tip Number 1

Familiarise yourself with the latest German and EU regulations related to pharmaceutical distribution, especially GDP requirements. This knowledge will not only help you in interviews but also demonstrate your commitment to staying updated in the field.

Tip Number 2

Network with professionals in the regulatory affairs sector, particularly those who have experience in the pharmaceutical industry. Attend relevant conferences or webinars to make connections and gain insights that could be beneficial during the application process.

Tip Number 3

Prepare to discuss your experience with CAPA, SOP drafting, and supplier audits in detail. Be ready to provide examples of how you've successfully managed these processes in previous roles, as this will showcase your hands-on expertise.

Tip Number 4

Highlight your leadership skills and ability to create an inspiring team environment. Think of specific instances where you've motivated a team or improved communication, as these qualities are crucial for the Regulatory Affairs Manager role.

We think you need these skills to ace Regulatory Affairs Manager

Regulatory Knowledge
Pharmaceutical Industry Experience
Quality Assurance Expertise
Good Distribution Practice (GDP) Understanding
Analytical Skills
Problem-Solving Skills
Attention to Detail

Some tips for your application 🫡

Tailor Your CV:Make sure your CV highlights your relevant experience in regulatory affairs, particularly in the pharmaceutical industry. Emphasise your skills in quality assurance, team management, and compliance with EU regulations.

Craft a Compelling Cover Letter:Write a cover letter that showcases your passion for regulatory affairs and your understanding of the role. Mention specific experiences that demonstrate your ability to lead teams and manage compliance effectively.

Highlight Relevant Skills:In your application, clearly outline your organisational skills, attention to detail, and problem-solving abilities. These are crucial for the role of Regulatory Affairs Manager and should be evident in your written application.

Proofread Your Application:Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is essential for this position.

How to prepare for a job interview at Astute Healthcare Ltd.

Showcase Your Regulatory Knowledge

Make sure to brush up on your knowledge of German and EU regulations related to pharmaceutical distribution. Be prepared to discuss how these regulations impact the role and how you have applied them in your previous positions.

Demonstrate Leadership Skills

As a Regulatory Affairs Manager, you'll be supervising a team. Share examples from your past experiences where you've successfully motivated and led a team, highlighting your ability to create an inspiring environment and foster open communication.

Prepare for Scenario-Based Questions

Expect questions that assess your problem-solving skills and ability to handle real-life situations, such as managing recalls or conducting audits. Think of specific instances where you effectively resolved issues and improved processes.

Highlight Your Organisational Skills

Given the importance of maintaining accurate quality records and documentation, be ready to discuss your organisational strategies. Provide examples of how you manage multiple priorities and ensure compliance with regulatory requirements.