Posted 10 days ago
Quality Specialist - Instrument Manufacturing (8 month FTC)
AI Summary
Manages product release activities for instrument manufacturing, handles customer complaints, and supports CAPA and market withdrawal processes. Creates, reviews, and approves quality documents and trains staff on quality topics.
About this role
Job Title
Quality Specialist - Instrument Manufacturing (8 month FTC)
Location(s)
TurkuAbout Us
Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world’s greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our team of 11,000+ colleagues from around the globe are vital to our success and the reason we’re able to push boundaries in pursuit of better human health.
Find your future at Revvity
Revvity is currently looking for a
Quality Specialist - Instrument Manufacturing
(Fixed term, 8 months)
Turku, Finland / Quality
Our Turku site, Wallac Oy, is one of the largest production and product development units within Revvity’s diagnostics business. Currently, more than 500 employees work in Turku. We develop and manufacture instruments, chemical reagents, and software for screening and research purposes. We are a market leader in providing screening systems for newborns and pregnant women, and our products are in use in over 100 countries.
Role Description:
Manage product release activities for instrument manufacturing.
Handle customer complaints related to instrument and software products, including customer communication.
Assist in the preparation, documentation, and follow-up of non-conformances and Corrective and Preventive Actions (CAPA).
Participate in market withdrawal and medical device reporting activities.
Create, revise, review, and approve quality-related documents, including SOPs, plans, and reports.
Track and trend quality-related data, including customer complaints.
Conduct training on quality-related topics for staff in Quality and other departments.
Collaborate closely with the Turku site and as part of the global Quality team
Role requirements:
B.Sc. or M.Sc. degree in Engineering, Computer Sciences, Bio/Health technology, or corresponding.
Experience in working in sustainable Quality Systems, preferably ISO 13485, QMSR or Pharma experience is also appreciated.
Effective cooperation and influencing skills, ability to work independently in a fast-paced environment.
Good written and verbal communication skills both in Finnish and English are essential.
We Offer:
Opportunity to work in an international company and develop your professional skills
A diverse and varied role
A committed and highly skilled organization
Revvity’s Turku site is a drug-free workplace, and a drug test is conducted for new employees as part of the pre-employment health check.
If you are interested and believe you are a good fit for the role, please submit your CV and application through our system before the 27th of September. We will begin reviewing applications during the application period.
For more information about the position, please contact the hiring manager Hanna Tähtinen hanna.tahtinen@revvity.com.
Skills
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