Senior Quality Control Analyst
Senior Quality Control Analyst
Senior Quality Control Analyst
Senior Quality Control Analyst
Proclinical Staffing
Pharma, Medizintechnik
Neuenburg
- Art der Anstellung: Vollzeit
- 77.000 CHF – 98.500 CHF (von XING geschätzt)
- Vor Ort
- Zu den Ersten gehören
Senior Quality Control Analyst
Über diesen Job
Senior Quality Control Analyst
- Job type: Contract
- Discipline: Good Manufacturing Practice (GMP)
- Location: Switzerland
Proclinical is seeking a Senior Quality Control Analyst to join a dynamic team in Neuchatel, Switzerland. This role focuses on ensuring high-quality standards in a fast-paced environment, with an emphasis on chromatographic and mass spectrometry techniques (HPLC, LC-MS). The position requires a proactive approach to problem-solving, continuous improvement, and adherence to cGMP standards.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
- Perform routine and non-routine quality control processes.
- Ensure compliance with cGMP, BPD, and EHS standards.
- Provide coaching and share knowledge on QC activities.
- Identify and resolve technical or organizational issues.
- Propose and implement technical or organizational solutions.
- Drive continuous improvement initiatives.
- Manage deviations, root cause analysis, and CAPA implementation using quality systems like Trackwise.
- Conduct regular GEMBA walks in the laboratory.
- Oversee critical reagents and ensure their availability for analyses.
- Act as a backup for method and equipment responsibilities.
- Participate in risk analyses for equipment and methods.
- Support regulatory submissions and inter-site harmonization of methods.
- Collaborate with suppliers for equipment maintenance and troubleshooting.
- Train analysts on specific methods, systems, and equipment.
Key Skills and Requirements:
- Strong laboratory experience, particularly in HPLC and LC-MS analysis.
- Solid understanding of biochemical methods and technologies.
- Familiarity with cGMP practices and quality systems.
- Fluent in French with technical proficiency in English.
- Swiss or EU nationality, or a valid Swiss work permit.
- Ability to thrive in a fast-evolving environment while maintaining high-quality results.
If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at a.bennett@proclinical.com.
Apply Now:
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