Company Overview:

Swiss Bioscience GmbH is a rapidly developing GMP manufacturing biotechnology company based in the Zurich Area, Switzerland. We specialize in the production and banking of human mesenchymal stem cells, catering to the evolving needs of regenerative medicine and biotechnology research.

Position Overview:

We are seeking a highly skilled Flow Cytometry Expert who will also serve as a Quality Control (QC) and Quality Assurance (QA) Specialist. The ideal candidate will be responsible for overseeing all aspects of flow cytometry analysis, ensuring the accuracy, reliability, and efficiency of experimental processes. Additionally, the candidate will play a pivotal role in maintaining and enhancing quality control and assurance protocols within our organization.

His/her main tasks will include:

Flow Cytometry Analysis:

• Perform flow cytometry experiments including sample preparation, data acquisition, and analysis.
• Develop and optimize flow cytometry protocols for various applications.
• Organize and manage flow cytometry data including acquisition files, analysis results, and experimental metadata.
• Prepare comprehensive reports summarizing experimental findings and quality control metrics.
• Troubleshoot technical issues related to flow cytometry instrumentation and data analysis software.

Data Management and Reporting:

• Organize and manage flow cytometry data including acquisition files, analysis results, and experimental metadata.
• Prepare comprehensive reports summarizing experimental findings and quality control metrics.
• Review and approve analytical data in accordance with GMP regulations and internal quality standards.
• Present findings to responsible manager and participate in scientific discussions and meetings.

Quality Control and Assurance:

• Promote good laboratory and manufacturing practices
• Design and implement quality control procedures for flow cytometry experiments and data analysis.
• Provide high-quality analytical support for manufacturing, ensuring compliance with protocols, cGMP, and safety regulations.
• Conduct regular quality audits to ensure compliance with established protocols and regulatory standards.
• Approve specifications, sampling instructions, and test methods.
• Collaborate with cross-functional teams to address any quality-related concerns and implement corrective actions.
• Manage, create, and review change controls, deviations, and CAPAs.
• Conduct investigations and risk assessments to support deviations and change controls.

Aseptic Work Environment and Equipment Maintenance and Calibration :

• Oversee the maintenance of aseptic work environments and coordinate regular maintenance of laboratory equipmentto ensure optimal performance.
• Coordinate with vendors for instrument servicing and repairs as needed.
• Manage orders, distribution, and inventory of materials for GMP QC department.
• Document instrument maintenance activities and update calibration records.

The candidate profile should include:

• BSc/MSc in the following field, cell biology, microbiology, chemistry, and Pharmacy, or Education as a laboratory technician,
• Proven extensive hands-on experience with flow cytometry instrumentation and data analysis software (e.g., Cytoflex, Fax, FlowJo, FCS Express).
• Basic knowledge of microbiology,
• Proven aseptic and laboratory work experience,
• Very Good MS Office and documentation skills,
• Excellent written and verbal communication inEnglish, as well as German, will be a plus (not required),
• Flexible to work with (not planned) shifts, weekends, and holidays is a must,
• Resolute and resilient team player with the ability to work under pressure and within a challenging environment,
• Careful and accurate working style, quality awareness; with a dedication to high quality and diligence paired with organizational skills,
• Excellent problem-solving skills with the ability to troubleshoot technical issues independently.
• Familiarity with regulatory requirements (e.g., GMP, ISO) for laboratory testing is a plus.
• Prior experience in a quality control role is preferred but not required.

If you are an enthusiastic collaborator with high diligence, excellent communication, and good organization skills; you are solution-oriented and autonomous, and you possess an initiative-taking working style, apply for this position.

Please, send your complete application (CV, short cover letter, references, and certificates/diplomas) to the following email addresses: Write an email and Write an email