About Our Client
Our client, a leading global player in the pharmaceutical industry located in the Lucerne area, is looking for a service and customer-oriented Quality Auditor (m/f/d) who will support the Quality Operations and Compliance organization on clinical quality activities, ensuring accountability for Good Manufacturing Practice (GMP) compliance. This role ensures that clinical supply functions operate within GMP requirements and compliant clinical drug substance and drug product supply.
Job Description
The selected candidate will be responsible for the following activities:
1. Oversight and support of certain quality assurance activities in Quality Operations and Compliance.
2. Conduct quality review and approval of GMP documentation (e.g., calibration activity documentation, equipment periodic review, logbooks, training plans and records, SOPs).
3. Support quality oversight activities under the responsibility of the Quality Operations and Compliance area (e.g., calibration, equipment periodic review, logbooks, management for training plans and training records, SOPs, quality on the floor).
4. Assure and maintain compliance with GMP regulations in the defined scope of work.
5. Provide support to projects and source areas as a Quality Assurance Representative.
The Successful Applicant
To be considered for this position, the ideal candidate must have:
1. BA/BS or higher academic education.
2. 3+ years of experience in a regulated industry, preferably in pharmaceuticals, biotechnology, or medical technology.
3. Experience in conducting quality oversight activities.
4. A focus on quality and compliance.
5. A service- and customer-oriented mindset.
6. Excellent communication skills and fluency in English; German is a plus.
What's on Offer
This is a unique opportunity to immediately join a renowned international company and become an integral part of the team.
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