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CQ Compliance Specialist
View: 132
Update day: 18-04-2024
Category: Finance / Bank / Stock Sales
Industry: Medical Equipment Manufacturing Biotechnology Research Pharmaceutical Manufacturing
Position: Mid-Senior level
Job type: Contract
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Job content
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.
- 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.
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Deadline: 02-06-2024
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