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Quality Engineer
- Permanent
- Good Manufacturing Practice (GMP), Good Clinical Practice (GCP)
- Switzerland
This vacancy has now expired. Please see similar roles below...
Proclinical is happy to announce that we are advertising an opportunity for a talented and hardworking individual to join a Quality Engineer position at a pharmaceutical company that specialises in fast-moving fields like software development, robotics, transportation, energy, and healthcare. This exciting company is seeking a talented and hard-working individual to join their team in Zurich.
Job Responsibilities:
- Implementing project and management of activities to define, design, develop and deliver new processes, quality improvement, and change initiatives.
- Leading and facilitating risk assessments for process and product development/improvement.
- Defining test strategies and guiding project teams on design controls.
- Developing products through process verification and validation.
- Implementing risk evaluation and writing up risk management solutions.
- Developing and implementing methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment.
- Leading Continuous Improvement projects around new product development and life-cycle management processes.
Skills and Requirements:
- A minimum of a bachelor's degree in Engineering, Life Sciences, or Physical Sciences.
- A Masters' degree in an engineering discipline strongly preferred.
- Electrical Engineering or related experience and/or training strongly preferred.
- At least 5 years of experience in the medical device, pharmaceutical, or other highly regulated industry preferred.
- Demonstrable experience in the Medical Device industry (FDA and ISO 13485).
- Six Sigma Certification (Green or Black) is preferred.
- Demonstrable experience with securing new businesses.
- Demonstrably high level of insight into design, development, and lifecycle management of products and processes.
- High-level of insight into statistical analysis of processes including statistical process control
- Strong understanding of risk evaluation and risk management for processes and product
- Working knowledge of statistical analysis software (e.g. Minitab)
- Strong team ethos, with a demonstrated track record of success in cross-functional teams and a fast-moving environment.
- An ability to manage multiple projects simultaneously to ensure timely, on-target, and within budget accomplishment of tasks.
- Strong communication, persuasion, presentation, and interpersonal skills.
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Josh Volpe on +44 203 800 1292 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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