Manufacturing Supervisor

  • Eysins, Switzerland
  • Full-time

Company Description

Building on 30 years of experience in transfusion diagnostics, Quotient is a commercial-stage
diagnostics company committed to delivering solutions that reshape the way diagnostics is practiced. MosaiQ™, Quotient’s proprietary multiplex microarray technology, offers the world’s first fully
automated, consolidated testing platform, allowing for multiple tests across different modalities.
MosaiQ™ is designed to be a game-changing solution, which Quotient believes will increase
efficiencies, improve clinical practice, deliver significant workflow improvements and operational
cost savings to laboratories around the world. Quotient’s operations are based in Eysins/Switzerland, Edinburgh/Scotland and Newtown/Pennsylvania.

Job Description

The Manufacturing Supervisor is responsible for managing a manufacturing team and leading the manufacturing floors operations including execution to procedures and schedule, personnel training, and containment/escalation of issues and deviations both within manufacturing and to support functions. His/her main activities will be:

  • Supervise the manufacturing team activities, including production, engineering and investigation run
  • Ensure the execution of qualifications, validations, process development, improvements or troubleshooting as per protocols
  • Implement and promote investigations based on root cause analysis tools
  • Implement and promote KPI’s to supervise all manufacturing activities
  • Work closely with the Bioprocess and Maintenance & Calibration supervisors to support a smooth coordination of the production technicians’ activities including safety, quality, scheduling, and performance
  • Promote and ensure the Good Manufacturing Practices, Good Documentation Practices and Safety guidelines are being followed correctly by the team
  • Ensure that all employees are trained on safety, quality and manufacturing procedures and that all procedures are followed in the facility
  • Manage employee performance through planning, monitoring, and appraising job results

Qualifications

  • Bachelor/Master’s degree and minimum 5-8 years of experience within a biotech / pharmaceutical manufacturing environment (Process Operations, Engineering or Quality
  • Minimum 7 years professional experience in performing manufacturing management with a strong experience within regulated industry / manufacturing environment
  • Relevant professional experience in Bioprocess optimisation or Technology transfers
  • Strong knowledge with EHS, ISO, cGMP, and regulatory requirements in a manufacturing environment
  • Excellent knowledge of IT tools (word, excel, quality system, ERP, MES)
  • Strong knowledge in engineering, problem solving and coordination of teams
  • Must be a team player and an effective communicator
  • Strong decision-making skills
  • Effective time management and prioritisation skills
  • Eagerness to work in a fast-paced, rapidly evolving environment requiring high flexibility
  • Fluent in English and French

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