Regulatory Affairs Manager - CMC

Proclinical is advertising a vacancy for a Regulatory Affairs Manager with a pharmaceutical company. This organisation is seeking an experienced and determined incumbent to join their team in Germany. This role is a contracted position, running for 12 months.

Job Responsibilities:

• Ensuring the quality of regulatory documentation (3 & 2.3).
• Preparing and updating the CMC documentation of international registration dossiers.
• CMC submissions.
• Providing regulatory support to multi-disciplinary projects.

Skills and Requirements:

• A degree in a Life Sciences field.
• At least 2 years of Regulatory Management experience.
• Effective time management, detail-oriented work style.
• Able to handle multiple tasks concurrently and in a timely fashion.
• Good interpersonal skills, including communication, persuasion, and leadership.
• Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
• Proficiency in MS Office.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Hugh Pickerill on +44 203 854 1079 or upload your CV on our website - www.Proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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