Quality Manager GCP

Proclinical are recruiting for a Quality Manager GCP to join a pharmaceutical organisation. This role is on a permanent basis and is located in Germany.

Responsibilities:

• Contribute to the development projects and monitor the interfaces within the scope or risk management.
• Perform personnel training and accompanying national and global regulatory inspections.
• Produce and revise audit programs.
• Assist with the development and upkeep of the quality management and SOP systems.
• You will prepare, implement, document and follow-up of audits for the company's clinical drug trials.

Key Skills and Requirements:

• Educated to a degree level in a life science/medical field or any other pertinent field such as natural science.
• Demonstrable experience within the field of drug development and practical experience in an auditing role.
• Keen to adapt to new work areas.
• Willing to travel for business needs.
• Expertise on guidelines and regulations such as US Code of Federal Regulations, Eudralex Volume 10, ICH-GCP, etc, for performing clinical trials in the pharmaceutical field.
• Competent in performing audits within a clinical field.
• Fluency in the English language.
• Communication skills both verbally and in writing.
• Computer literacy.
• Works well independently with a goal focused mindset.

If you are having difficulty in applying or if you have any questions, please contact Antoine Mortiaux at + 49 6950608631.

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

Proclinical Staffing is an equal opportunity employer.

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