Senior MedTech QA/RA Consultant — Regulatory Strategy

Prevas; Stockholms kommun; On-site; SEK 650,000 - 950,000; Full time

Job summary

A technology company in Sweden is looking for an experienced regulatory affairs professional to develop strategies for market entry in the EU, UK, Switzerland, and USA. The role requires 5+ years in regulatory and quality affairs for medical devices, with a strong collaborative spirit and integrity. This position promises exciting projects, supportive colleagues, and an inspiring work culture that values community and participation.

Qualifications

• 5+ years of experience in regulatory affairs and/or quality for medical devices.
• Strong knowledge of regulatory and quality requirements throughout medical device development.
• Ability to work effectively in a collaborative team environment.

Responsibilities

• Develop regulatory strategies for market entry in multiple regions.
• Support implementation of management systems and technical documentation.
• Engage with stakeholders during product submissions and approvals.

Skills

Regulatory affairs experience

Quality management expertise

Team collaboration

Positive attitude

Job description

A technology company in Sweden is looking for an experienced regulatory affairs professional to develop strategies for market entry in the EU, UK, Switzerland, and USA. The role requires 5+ years in regulatory and quality affairs for medical devices, with a strong collaborative spirit and integrity. This position promises exciting projects, supportive colleagues, and an inspiring work culture that values community and participation.