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 proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
What you’ll do
Maintain calibration systems and their procedure for the site
Analyse and solve calibration problems using advanced mathematical and engineering knowledge
Develop and/or improve process for calibration/measurement
Use statistical process control to analyse measurement standards and processes
Recommend calibration standards
Define internal or external lab verification for equipment
Coordinates instrument testing with owning departments
Consistently achieve and sustain KPI’s for QC and Manufacturing
Perform calibrations on equipment and/or coordinate with external calibration companies
Conduct planned and unplanned maintenance on production equipment
Write maintenance procedures and reports
Maintain the necessary critical spare parts components supporting equipment through Inventory Control.
Act as Subject Matter Expert for the metrology process for the site
Perform additional duties as required
Who you are
Bachelor’s degree and a minimum of 3 years’ experience in Mechanics or Manufacturing Engineering, or other comparable technical degree with related experience in pharmaceutical or medical device
Knowledge of ISO 17025 accreditation
Knowledge of 3D dimensional control machine
Understanding of current manufacturing processes and best practices (equipment, robotics, non-conformance procedures, etc.)
Experience in process development, acceptance testing and qualification of equipment.
Analytical spirit and data driven
English, French language
Project management experience
When you join us, you’ll also be joining Danaher’s global organization, where 68,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.
Danaher is committed to a diverse and inclusive culture where everyone feels they belong and all voices are heard. We believe in our associates and the unique perspectives they bring to every challenge, which is why we’ll empower you to push the boundaries of what’s possible.
If you’ve ever wondered what’s within you, there’s no better time to find out.