Regulatory Affairs CMC Manager contract
Regulatory Affairs CMC Manager contract

Regulatory Affairs CMC Manager contract

Cambridge Full-Time 48000 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead the creation of CMC documents for global regulatory submissions.
  • Company: Join a dynamic pharmaceutical company with a strong reputation in the industry.
  • Benefits: Enjoy flexible working options and potential for contract extension.
  • Why this job: Be part of a collaborative team making a real impact in global health.
  • Qualifications: Must have significant Regulatory CMC experience and dossier preparation skills.
  • Other info: This is a 12-month contract with hybrid working in Cambridge.

The predicted salary is between 48000 - 72000 £ per year.

Regulatory Affairs CMC Manager, contract job
Your new company
This pharmaceutical company is looking for an experienced Regulatory Affairs CMC professional to join an established team on a contracting basis. This is a 12-month contract job with scope for extension, hybrid working is available, and there will be a need for an onsite presence in Cambridge.
Your new role
As Regulatory Affairs CMC Manag…

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Regulatory Affairs CMC Manager contract employer: Hays

This pharmaceutical company is an excellent employer, offering a dynamic work environment in the heart of Cambridge, where innovation meets collaboration. With flexible working options and a strong emphasis on employee growth, you will have the opportunity to enhance your skills while contributing to impactful regulatory submissions across diverse international markets. Join a supportive team that values your expertise and fosters a culture of continuous improvement and professional development.
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Contact Detail:

Hays Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Regulatory Affairs CMC Manager contract

✨Tip Number 1

Make sure to highlight your experience with CMC regulatory submissions in your conversations. Discuss specific projects where you successfully coordinated the preparation of CMC documents, as this will demonstrate your expertise and relevance for the role.

✨Tip Number 2

Network with professionals in the pharmaceutical industry, especially those who have worked in Regulatory Affairs. Attend relevant conferences or webinars to connect with potential colleagues and learn more about current trends in CMC regulations.

✨Tip Number 3

Familiarize yourself with the specific regulatory requirements for the regions mentioned in the job description (Asia, Latin America, Middle East, Eastern Europe, and Africa). Being knowledgeable about these areas can set you apart from other candidates.

✨Tip Number 4

Prepare to discuss how you manage relationships with external partners and internal teams. Your ability to collaborate effectively will be crucial in this role, so be ready to share examples of successful teamwork in your previous positions.

We think you need these skills to ace Regulatory Affairs CMC Manager contract

Regulatory CMC Expertise
CMC Document Preparation
Regulatory Submissions
Pharmaceutical Development Knowledge
Quality Assurance (QA) Collaboration
International Regulatory Knowledge
Project Management Skills
Attention to Detail
Communication Skills
Problem-Solving Skills
Stakeholder Management
Experience with Marketing Applications
Knowledge of Regulatory Authorities
Adaptability to Changing Regulations

Some tips for your application 🫡

Understand the Role: Make sure to thoroughly read the job description for the Regulatory Affairs CMC Manager position. Understand the key responsibilities and required skills, especially focusing on CMC document preparation and regulatory submissions.

Highlight Relevant Experience: In your CV and cover letter, emphasize your significant experience in Regulatory CMC. Provide specific examples of CMC regulatory dossiers you have prepared and any successful interactions with regulatory authorities.

Tailor Your Application: Customize your application materials to reflect the requirements of the job. Use keywords from the job description, such as 'pharmaceutical development', 'marketing applications', and 'regulatory submissions' to demonstrate your fit for the role.

Proofread Your Documents: Before submitting your application, carefully proofread your CV and cover letter. Ensure there are no grammatical errors or typos, as attention to detail is crucial in Regulatory Affairs.

How to prepare for a job interview at Hays

✨Showcase Your CMC Expertise

Make sure to highlight your significant experience in Regulatory CMC during the interview. Be prepared to discuss specific examples of CMC regulatory dossiers you have prepared and finalized, as well as how you managed existing product licenses.

✨Understand Global Regulatory Requirements

Familiarize yourself with the regulatory requirements in the regions mentioned in the job description, such as Asia, Latin America, and Eastern Europe. Demonstrating knowledge of these areas will show that you are well-prepared for the role.

✨Emphasize Collaboration Skills

Since the role involves working with various teams like pharmaceutical development, manufacturing, and QA, be ready to discuss your experience in cross-functional collaboration. Share examples of how you successfully coordinated with different stakeholders.

✨Prepare for CMC Questions

Anticipate questions related to CMC challenges and how you would respond to inquiries from regulatory authorities. Think about past experiences where you effectively addressed CMC questions and be ready to share those insights.

Regulatory Affairs CMC Manager contract
Hays
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  • Regulatory Affairs CMC Manager contract

    Cambridge
    Full-Time
    48000 - 72000 £ / year (est.)

    Application deadline: 2027-02-03

  • H

    Hays

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