Process Engineer

Vitrolife Sweden Aktiebolag; Göteborgs kommun; On-site; SEK 500,000 - 700,000; Full time

Job summary

Vitrolife Sweden Aktiebolag is searching for a Process Engineer to enhance our production capabilities at our Gothenburg office. This position demands expertise in automation and mechatronic, complemented by a strong background in quality standards and collaborative skills.

The successful candidate will lead the development and implementation of new manufacturing processes, driving continuous improvements while ensuring compliance with ISO-13485 and GMP. Candidates must hold a relevant degree and possess at least 5 years of experience in the automation field.

Qualifications

• Previous experience working in automation or mechatronic roles for at least 5 years.
• Strong understanding of quality standards and production processes.
• Ability to work collaboratively with cross-functional teams.

Responsibilities

• Develop and implement production processes.
• Drive continuous improvements across production departments.
• Ensure compliance of current production processes.
• Collaborate with QA, Supply Chain, and Product Development on outsourced product processes.

Skills

Automation/mechatronic expertise

Quality standards ISO-13485 and GMP

Fluent in Swedish

Proficient in English

Education

Bachelor or master's degree in biomedicine, chemistry, biology, mechanic, automation

Job description

About the Role

We are looking for a Process Engineer. This team will consist of different competencies, such as biomedicine, biotechnique, validation, automation and mechatronic. You will be responsible for automation/mechatronic knowledge within the department. You will also be responsible for one of our manufacturing processes and drive the work with continuous improvements. Whenever there is a question regarding automation/mechatronic from your colleagues you will be asked to help. This is a team with a lot of cross‑functional collaborations and responsibilities with both internal and external stakeholders from a variety of countries.

Key Responsibilities

• Developing and implementing new production processes
• Driving continuous improvements on existing processes in close collaboration with all production departments
• Ensuring that existing production is compliant for all in‑house production within the business area
• Work with outsourced products and the assessment and approval of suppliers’ processes in close collaboration with Quality Assurance, Supply Chain and Product Development

This is a permanent, full‑time position based at our office in Gothenburg. Travel and work from other Vitrolife sites and contract manufacturers might be part of the position.

Your Profile

• Bachelor or master's degree in biomedicine, chemistry, biology, mechanic, automation or equivalent
• Experience working with quality standards and processes (ISO‑13485, GMP)
• 5 years’ experience of automation/mechatronic work
• Fluent in Swedish and good knowledge in English both oral and written
• Thorough, structured, able to see the whole picture, prioritize and meet deadlines; service‑oriented, solution‑focused and communicative; enjoy working in a changing and dynamic environment