At a Glance
- Tasks: Lead operations teams in evaluating non-conformances and managing quality engineers' development plans.
- Company: Cytiva is a leader in the Life Sciences industry, part of Danaher, with a mission to improve human health.
- Benefits: Opportunities for continuous learning and career growth across 40 countries.
- Other info: The role involves working cross-functionally to enhance compliance and reduce complaints.
- Why this job: Join a team dedicated to life-saving innovations in vaccines and therapies.
- Qualifications: Experience in quality/engineering leadership and conducting QMS audits is preferred.
The predicted salary is between 45000 - 55000 £ per year.
Be part of something altogether life-changing! Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva, you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Cytiva is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.
What you'll do:
- Support and lead the operations teams and engineers when required in the evaluation, trending and reporting of internal and external non-conformances to establish priorities and identify common threads aimed at a continuous reduction in internal non-conformance occurrences via internal or supplier process improvements.
- Develop, manage and maintain the development plans for the quality engineers in QA.
- Actively review the production environment identifying non-conformity, areas to improve compliance.
- Coordinate and report relevant failure investigations and subsequent corrective and preventive actions and review their effectiveness.
- Work with the engineers to collect, analyse, trend and report data on rejects from routine production inspections and QC tests and related processes to establish improvement priorities and identify common threads aimed at a reduction in external complaints.
- Work with QA specialists and others as appropriate to ensure that production inspections and QC tests are aligned with customer needs.
Who you are:
- Ability to lead others when working within a cross-functional team.
- Logical, inquiring approach to work.
- Must be motivated and able to work to deadlines.
- Ability to work without supervision, using own initiative, prioritising work as appropriate whilst maintaining a cross-functional team approach.
- Able to make reasoned and objective decisions where necessary and communicate these in an effective manner.
It would be a plus if you also possess previous experience in:
- Quality/engineering leadership.
- Lead and facilitate Kaizen events/improvement activities.
- Conduct QMS and manufacturing audits.
Senior Quality Engineer in Newquay employer: Job Search Place Limited
Cytiva, located globally, is committed to transforming human health through innovative solutions. Employees enjoy continuous learning opportunities and career growth while contributing to life-saving projects. The team values collaboration and care for customers and patients alike.
