Quality Specialist

Revvity; Turku; On-site; EUR 45,000 - 65,000; Full time

Benefits offered by this job

International company culture

Diverse role

Professional development

Job summary

Revvity's Turku site (Wallac Oy) is seeking a Quality Specialist to join our growing diagnostics business. You will handle customer complaints, support post-market surveillance, and help create and approve quality documents, SOPs and CAPA plans.

Ideal candidates hold a B.Sc. or M.Sc. in Engineering or Bio/Health technology, have 3–5 years of experience with ISO 13485 or QMS, and communicate well in Finnish and English while working in a fast-paced, international environment.

Qualifications

• B.Sc. or M.Sc. in Engineering, Bio/Health technology, or equivalent.
• 3–5 years in sustainable Quality Systems; ISO 13485/QMSR or pharma experience is a plus.
• Strong collaboration and communication skills in Finnish and English.

Responsibilities

• Handle customer complaints related to instruments and reagents.
• Conduct post-market surveillance and related quality activities.
• Create, revise, review, and approve quality documents including SOPs, plans, and reports.
• Support CAPA processes and follow-up.
• Track and trend quality data including customer complaints.
• Deliver quality training to personnel.

Skills

Quality collaboration

Independent worker

Excellent communication

Education

B.Sc. or M.Sc. in Engineering/BioHealth technology

Tools

ISO 13485

Job description

Turku, Finland
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
Turku, Finland
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

• Handling customer complaints related to instruments and reagents
• Conducting post-market surveillance and related quality activities
• Creating, revising, reviewing, and approving quality-related documents, including SOPs, plans, and reports
• Supporting the preparation, documentation, implementation, and follow-up of Corrective and Preventive Actions (CAPA)
• Tracking and trending quality-related data, including customer complaints
• Delivering training on quality-related topics to personnel in Quality and other departments
• Working closely with the Turku site and collaborating as part of the global Quality team
  

Role requirements

• B.Sc. or M.Sc. degree in Engineering, Bio/Health technology, or corresponding.
• 3-5 years 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.
For more information about the position, please contact the hiring manager Hanna Tähtinen [e-mail].