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- Aufgaben: Join our Life Sciences team to manage analytical assays and support daily QC activities.
- Arbeitgeber: We are a leading player in the pharmaceutical sector, committed to quality and compliance.
- Mitarbeitervorteile: Enjoy a diverse workplace with opportunities for growth and development.
- Warum dieser Job: Make an impact in the biotech field while working in a supportive and innovative environment.
- Gewünschte Qualifikationen: Bachelor/Master in Engineering or equivalent with 3 years of relevant experience required.
- Andere Informationen: Fluency in French and English is essential; we value diversity and welcome all qualified candidates.
Das voraussichtliche Gehalt liegt zwischen 36000 - 60000 € pro Jahr.
Quality Control Specialist (F/M)
To join our Life Sciences team in Neuchâtel, we are looking for a Quality Control Specialist (F/M) in the pharmaceutical sector.
The job holder is accountable for life cycle management activities of analytical assays performed in the QC Laboratories with a focus on:
- Laboratory Investigations
In addition, the job holder also supports daily QC activities following cGMP, client’s policies and EHS requirements.
Validation and Qualification Activities
- Author transfer protocols and reports for assays
- Author qualification plans and reports for critical reagents
- Oversee validation and qualification activities executed by analysts, provide training and support
- Execute and document experiments
Investigation Leads
- Investigate and troubleshoot problems which occur to determine solutions or recommendations for improvements or change
- Conduct/participate in risk assessments, root cause analysis and investigations
- Own Laboratory Investigations and CAPA
Quality Control Support Activities
- Support the application of industry specific compliance standards/regulations to assays life cycle management activities
- Participate in daily activities upon request (provide technical and statistical support)
Minimum Requirements:
- Bachelor/Master in Engineering field (chemical, biotechnology) or equivalent
- 3 years of experience within a biotech/pharmaceutical GMP manufacturing environment
- Good knowledge of method transfer
- Good knowledge of critical reagent qualification
- Experience in problem solving and deviation management
- Good knowledge of statistical tools
- Proficiency in all aspects of standard IT tools
- Fluent in French and English
Our positions are open to people who have been recognized as disabled workers. T&S Group promotes diversity and equality in the workplace. All qualified M/F candidates are considered for employment on an equal basis.
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Quality Control Specialist (F/M) Arbeitgeber: Antaes Consulting SA
Kontaktperson:
Antaes Consulting SA HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Quality Control Specialist (F/M)
✨Tip Number 1
Familiarize yourself with cGMP regulations and industry-specific compliance standards. This knowledge will not only help you in interviews but also demonstrate your commitment to quality control in the pharmaceutical sector.
✨Tip Number 2
Highlight your experience with laboratory investigations and problem-solving. Be prepared to discuss specific examples where you've successfully identified issues and implemented solutions in a QC environment.
✨Tip Number 3
Showcase your proficiency in statistical tools and IT applications relevant to quality control. Being able to analyze data effectively is crucial for this role, so be ready to talk about your experience with these tools.
✨Tip Number 4
Since the position requires fluency in both French and English, practice discussing technical topics in both languages. This will prepare you for potential interviews and show that you're ready to communicate effectively in a bilingual environment.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Quality Control Specialist (F/M)
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Quality Control Specialist position. Understand the key responsibilities and required qualifications, as this will help you tailor your application.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in the biotech or pharmaceutical sector, particularly in GMP environments. Mention specific projects or tasks that relate to laboratory investigations, validation, and quality control.
Showcase Technical Skills: Detail your proficiency with statistical tools and IT applications relevant to quality control. If you have experience with method transfer or critical reagent qualification, make sure to include that as well.
Language Proficiency: Since the role requires fluency in both French and English, ensure that your language skills are clearly stated in your application. You might also want to provide examples of how you've used these languages in a professional context.
Wie du dich auf ein Vorstellungsgespräch bei Antaes Consulting SA vorbereitest
✨Show Your Technical Knowledge
Make sure to highlight your understanding of cGMP regulations and quality control processes. Be prepared to discuss specific experiences where you applied these principles in a biotech or pharmaceutical setting.
✨Demonstrate Problem-Solving Skills
Prepare examples of how you've successfully investigated and resolved issues in previous roles. Discuss your approach to root cause analysis and any tools you used to support your findings.
✨Emphasize Team Collaboration
Quality Control Specialists often work closely with other teams. Share experiences that showcase your ability to collaborate effectively, provide training, and support colleagues in validation and qualification activities.
✨Be Ready for Technical Questions
Expect questions related to method transfer and critical reagent qualification. Brush up on relevant statistical tools and be ready to explain how you've utilized them in your past work.
