Senior Product Developer – Medical Devices

Moveup Consulting AB; Göteborgs kommun, Strömstads kommun; Hybrid; SEK 800,000 - 1,100,000; Full time

Benefits offered by this job

Flexible working arrangements

Collaborative work environment

Opportunity for continuous learning

Job summary

A leading medical devices company is seeking a Senior Product Developer in Gothenburg. In this role, you'll lead the development of new medical device products and manage the lifecycle of existing ones. Your responsibilities will include driving technical improvements, ensuring regulatory compliance, and collaborating across functions to deliver robust products. The ideal candidate will have strong experience in medical device product development and a relevant degree. Flexible working arrangements and a comprehensive compensation package are offered.

Qualifications

• Strong experience in medical device product development or a closely related regulated environment.
• Practical knowledge of ISO 13485, ISO 14971, and EU MDR.
• Hands-on experience in a product development or verification laboratory.
• Experience with material-based medical devices is a strong advantage.
• Experience with materials-based medical devices and rheology is a plus.

Responsibilities

• Lead hands-on development of new medical device products from concept to design transfer.
• Drive technical improvements and lifecycle management of existing products.
• Act as technical product owner with deep understanding of design and performance.
• Plan and perform development and verification testing in laboratory.
• Execute design control activities per ISO 13485.
• Maintain the Design History File (DHF) during development and changes.
• Plan and perform verification testing in lab or with external partners.
• Ensure compliance with ISO 13485, ISO 14971, and EU MDR.
• Analyze post-market data and contribute to product improvements.

Skills

Medical device product development

Hands-on development

ISO 13485 knowledge

Analytical capability

Technical leadership

Materials and rheology

Engineering degree

Cross-functional collaboration

Education

Degree in engineering, biotechnology, chemistry, or medical technology

Tools

Laboratory testing equipment

Job description

Senior Product Developer – Medical Devices

Are you an experienced product developer within medical devices who enjoys combining hands-on innovation, laboratory work, and technical leadership?

We are looking for a Senior Product Developer who will take a key role in developing new medical device products while also driving improvements and lifecycle management of an existing product portfolio.

This is an exciting opportunity to join a growing and agile organisation where you will have a strong influence on product development, technical decisions, and the future direction of the product portfolio.

The Role

As a Senior Product Developer, you will act as the technical owner of assigned products, leading development activities from concept through design transfer, while ensuring compliance with applicable regulatory and quality requirements.

You will take ownership of technical decisions related to product design, testing strategies, and development activities within the approved scope, and prioritize development and improvement initiatives to drive both new product development and continuous improvement of existing products.

The role also includes structuring and operating the product development laboratory, planning verification activities, and working cross-functionally with QA/RA, manufacturing, supply chain, and commercial teams to ensure that products are technically robust, compliant, and ready for market.

Key Responsibilities

• Lead hands-on development of new medical device products from concept to design transfer
• Drive technical improvements and lifecycle management of existing products
• Act as technical product owner with deep understanding of design, materials, performance, and intended use
• Plan and lead product development projects, including scope, milestones, and timelines
• Execute and maintain design control activities according to ISO 13485
• Own and maintain the Design History File (DHF) during development and product changes
• Plan and perform development and verification testing in the laboratory or with external partners
• Ensure compliance with ISO 13485, ISO 14971, and EU MDR requirements
• Analyse post-market data and contribute to continuous product improvement

Your background

We believe you bring a combination of strong technical and analytical capability, and hands‑on product development experience.

We’re looking for someone with:

• Strong experience in medical device product development or a closely related regulated environment
• Practical knowledge of ISO 13485, ISO 14971, and EU MDR
• Hands‑on experience working in a product development or verification laboratory, including planning, executing, and documenting tests
• A degree in engineering, biotechnology, chemistry, medical technology, or similar
• Experience with material‑based medical devices (e.g., hydrogels or polymer systems) and rheological characterization is considered a strong advantage.

Who you are

To thrive in this role, you are someone who:

• Enjoys combining hands‑on development with strategic thinking
• Works in a structured and pragmatic way while solving technical challenges
• Is comfortable taking ownership and driving projects forward
• Enjoys collaborating across functions in a dynamic and entrepreneurial environment

What can we offer

• Opportunity to lead product development and shape the future of our product portfolio.
• Work in a small, collaborative team with short decision paths, where you have real influence over products, processes, and outcomes.
• A collaborative, dynamic work environment with cross‑functional teams, where we care with purpose, treat colleagues with respect, and foster a supportive culture.
• A workplace driven by curiosity and continuous learning, encouraging open communication for better decisions.
• Empowered accountability: take ownership of your work and see the impact of your contributions.
• Flexible working arrangements, including partial remote work after an initial hybrid onboarding period.
• Compensation package that reflects your responsibility, contribution, and the impact you will make.

In this recruitment Bohus Biotech is collaborating with Moveup Consulting. For questions regarding the position, please contact Tom Bergqvist at [e-mail]

By submitting your application, you also consent to us storing your personal data, including your CV and cover letter, and you agree that we have the right to share this information with third parties (our client). You can withdraw your consent at any time.

Founded in 1993, BOHUS has been at the forefront of Hyaluronic Acid (HA) development and manufacturing for over three decades. Our journey began with a vision to revolutionize the HA industry through innovation and commitment to excellence.

With more than 30 years of expertise, the company has established a strong international presence with products distributed to hospitals, clinics, and physicians in over 60 countries worldwide.

Bohus Biotech focuses exclusively on high quality hyaluronic acid technologies across three therapeutic areas:

• Ophthalmology – OVD solutions supporting tissue protection during cataract surgery
• Aesthetics – Dermal fillers based on the proprietary SHAPE™ technology platform
• Orthopaedics – Injectable treatments for osteoarthritis

All research, development, and manufacturing are in Strömstad, Sweden, ensuring full control over product quality and innovation. For more information, visit the company’s web sites at: www.bohusbiotech.com

Se mer

Email

Policy Jag samtycker till att Moveup lagrar mina personuppgifter i syfte att kontakta mig för information och erbjudanden. Detta samtycke kan när som helst återkallas. Läs mer i vår integritetspolicy .