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- Aufgaben: Join our team to review and release clinical supplies and ensure quality compliance.
- Arbeitgeber: Be part of a global biopharmaceutical company based in beautiful Lucerne.
- Mitarbeitervorteile: Enjoy a hybrid work model with flexibility between home and office.
- Warum dieser Job: Gain valuable experience in a regulated environment while contributing to impactful healthcare solutions.
- Gewünschte Qualifikationen: A university degree and 2 years of experience in a regulated field are preferred.
- Andere Informationen: Training starts fully on-site before transitioning to a hybrid model.
Das voraussichtliche Gehalt liegt zwischen 43200 - 72000 € pro Jahr.
CK QLS are looking for a Specialist Clinical Supplies Quality to join a Global Biopharmaceutical company, based in Lucerne. Duration: From 1st of May to 31st of December 2025. Home Office: We do have a hybrid work model. The candidate will start for training purposes fully on site and then switch to hybrid (currently 2 days in the office, 3 days home office), which might change depending on business needs. Responsibilities: Review and release of incoming label stock. Review and release of clinical finished goods, including review of the printed and applied label. GMP review of the batch record and review of the regulatory filings and the final release. Candidate’s Requirements: Previous experience in a similar role is highly appreciated; a university degree (bachelor or higher) is preferred; experience in a regulated environment is an advantage. Minimum of 2 years experience in a regulated environment (pharma, medtech preferred). English C1 mandatory; German is nice to have. Day in the job: Three times per week, the day starts at 9, with a team meeting to discuss ongoing jobs to be released (batch). During a day, the person will work on releases. Apply: If you are interested, please send a CV in English to Please quote job reference 122 377 in all correspondence. #J-18808-Ljbffr
Quality Auditor III Arbeitgeber: Whatjobs
Kontaktperson:
Whatjobs HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Quality Auditor III
✨Tip Number 1
Make sure to familiarize yourself with Good Manufacturing Practices (GMP) and the specific regulations in the biopharmaceutical industry. This knowledge will not only help you during the interview but also demonstrate your commitment to quality standards.
✨Tip Number 2
Network with professionals in the biopharmaceutical field, especially those who have experience in quality auditing. Engaging with them can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Prepare for the team dynamics by understanding how hybrid work models function. Be ready to discuss your adaptability to both in-office and remote work settings, as this is crucial for the role.
✨Tip Number 4
Brush up on your English language skills, particularly at a C1 level, as this is mandatory for the position. Consider practicing technical vocabulary related to quality assurance and regulatory compliance.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Quality Auditor III
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Quality Auditor III position. Understand the responsibilities and requirements, especially the importance of experience in a regulated environment.
Tailor Your CV: Customize your CV to highlight relevant experience in quality assurance and regulatory compliance. Emphasize any previous roles in the pharmaceutical or medtech industries, and ensure your English proficiency is clearly stated.
Craft a Strong Cover Letter: Write a compelling cover letter that addresses why you are a good fit for this role. Mention your experience with GMP reviews and your ability to work in a hybrid model, as well as your willingness to adapt to business needs.
Follow Application Instructions: When submitting your application, make sure to include the job reference 122 377 in all correspondence. Double-check that your CV is in English and that all documents are properly formatted before sending.
Wie du dich auf ein Vorstellungsgespräch bei Whatjobs vorbereitest
✨Showcase Your Relevant Experience
Make sure to highlight your previous experience in a regulated environment, especially in pharma or medtech. Be prepared to discuss specific examples of how you've handled quality audits or GMP reviews in your past roles.
✨Demonstrate Your Knowledge of GMP
Since the role involves GMP review of batch records, brush up on your knowledge of Good Manufacturing Practices. Be ready to explain how you ensure compliance and quality in your work.
✨Prepare for Team Dynamics
As the job involves regular team meetings, think about how you can contribute to team discussions. Prepare to share your thoughts on ongoing projects and how you can support your colleagues in achieving their goals.
✨Language Skills Matter
While English is mandatory, having German skills is a plus. If you speak German, be sure to mention it during the interview, as it could set you apart from other candidates.
