Quality Specialist (8 month FTC)

Revvity; Turku; On-site; EUR 42,000 - 64,000; Full time

Benefits offered by this job

International company

Diverse role

Committed organization

Job summary

Revvity’s Turku site in Finland is seeking a Quality Specialist for an 8-month fixed-term role. You will manage product release for instruments, handle customer complaints, and lead CAPA activities while collaborating with global Quality teams.

The ideal candidate holds a B.Sc./M.Sc. in engineering or health tech, has QA system experience (ISO 13485 preferred), and communicates well in Finnish and English. On-site work in Turku is expected.

Qualifications

• B.Sc. or M.Sc. degree in Engineering, Computer Sciences, Bio/Health technology, or corresponding.
• Experience with ISO 13485 or QA systems; pharma experience is a plus.
• Excellent written and spoken Finnish and English.

Responsibilities

• Manage product release activities for instrument manufacturing.
• Handle customer complaints related to instrument and software products, including customer communication.
• Assist in preparation, documentation, and follow-up of non-conformances and CAPA.
• Participate in market withdrawal and medical device reporting activities.
• Create, revise, review, and approve quality-related documents (SOPs, plans, reports).
• Track and trend quality data, including customer complaints.
• Conduct training on quality topics for staff across Quality and other departments.
• Collaborate with the Turku site and the global Quality team.

Skills

Cooperation skills

Influencing skills

Independent worker

Fast-paced environment

Education

B.Sc. or M.Sc. degree in Engineering, Computer Sciences, Bio/Health technology, or corresponding

Job description

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.

Revvity is currently looking for a

Quality Specialist

(Fixed term, 8 months)

Turku, Finland / Quality

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.

Please contact the hiring manager Hanna Tähtinen [e-mail].