CQ Compliance Specialist

Proclinical are recruiting a CQ Compliance Specialist for a pharmaceutical organisation. This role is on a contract basis and is located in Visp.

Responsibilities:

• Evaluate incidents reports and change documents with the framework of project CQ plan, site and international processes.
• Arrange evaluation session for all pertinent commissioning and qualification document.
• You will keep track of lifecycle documents and update the documentation trackers.
• Mediate with the project documentation control division and QA representatives.
• Assist the CQV lead in offering technical guidance and direction for CQV actions.
• Recognise prospects for constant improvement and execute alterations to optimise CQV procedures.
• Other duties may be assigned to this role.

Key Skills and Requirements:

• Familiarity in Commissioning, Qualification and Validation especially in project setting.
• Capable of leading CQ document preparation and/or CQ implementation team in CQ and compliance features.
• A flexible individual with the ability to handle and adapt to necessary situations to deliver the project with the right quality in a timely manner.
• Fluency in the English language with knowledge in German.
• Know-how of typical tools and software used in a pharma/biotech organisation.
• Expertise on Kneat would be beneficial for the role.
• A positive mindset.
• Capable of working within a globally diverse team.

If you are having difficulty in applying or if you have any questions, please contact Chloe Jack at +41 61 508 73 40.

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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