At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we help our customers and their patients to fulfill the dream of having a baby.
About the role
We are now 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 continues 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 our in-house production within the business area
Process engineering will also work with our outsourced products and the assessment and approval of our suppliers’ processes in close collaboration with our Quality Assurance, Supply Chain and Product Development department.
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
Experiences from 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
You are thorough, structured, can see the whole picture and are able to prioritize and meet deadlines. You are also service-oriented, solution-focused and communicative and you enjoy working in a changing and dynamic environment.
Applications will be reviewed on an ongoing basis, so please submit your application as soon as possible.
Vitrolife Group is a global provider of medical devices and genetic services. Based on science and advanced research capabilities, we develop services and products for personalized genetic information and medical device products. We support our customers by improving their clinical practice for the patient's outcome of fertility treatment.
We are currently approximately 1 100 colleagues worldwide, with headquarters in Gothenburg, Sweden. Vitrolife Group's products and services are available in more than 110 countries through our own presence in 30 countries and a network of distributors. Vitrolife Group is a sustainable market leader and aims to be the preferred partner for IVF-clinics by providing superior products and services with the vision of fulfilling the dream of having a baby. The Vitrolife share is listed on Nasdaq Stockholm.
Skills Required
- Bachelor or master's degree in biomedicine, chemistry, biology, mechanic, automation or equivalent
- Experience working with quality standards and processes (ISO-13485, GMP)
- Minimum 5 years' experience in automation/mechatronic work
- Fluent in Swedish and strong written and spoken English
What We Do
Vitrolife Group is a global provider of medical devices and genetic testing services for reproductive health and assisted reproduction. The company develops, manufactures, and markets fertility products and advanced software, including time-lapse incubators and embryo evaluation systems. Its mission is to help people fulfill the dream of having a healthy baby, supporting fertility clinics and patients worldwide through innovation and research.
