Quality and Environmental Manager

Nolato MediTech develops and manufactures polymer products and systems in close collaboration with leading customers in medical technology and pharmaceuticals. We are world leaders in silicone injection molding and have extensive experience in plastic injection molding for medical technology, with specialized expertise in 2K and 3K processes. We also offer innovative solutions in further processing and assembly. Nolato MediTech has two production facilities in southern Sweden. Cleanroom production class 8 and hygiene production according to ISO 14644-1. Certified according to ISO 9001, ISO 13485, and ISO 14001, and FDA-registered. We are seeking a Quality and Environmental Manager to continue developing the business toward world-class standards. As a leader with us, you are a manager, teacher, and coach in the application of the working methods and processes we follow. There is structure for the work, but we want you to continuously challenge it through your presence and active leadership, which will determine the results achieved. You must be able to make quick decisions while thinking long-term. The role includes strategic planning for your department, which is then broken down into clear objectives with a daily structure. In this role, you have personnel responsibility for 6 quality engineers and are responsible for the factory's quality and environmental work. Main Responsibilities: Lead and develop your team's competence and working methods Train and guide the organization in meeting quality systems and customer requirements Define customer requirements, document control, and monitoring of regulatory requirements Responsible for the factory's deviation and complaint handling Responsible for the factory's quality and environmental work Conduct audits, internal and external Represent the factory at customer and third-party audits Continuously improve and develop the factory's quality and environmental work Qualifications and Experience You are an experienced leader with strong knowledge of quality work in a manufacturing, medical technology, and/or pharmaceutical manufacturing industry. We believe you have a relevant university degree or equivalent experience. You have worked for at least five years with quality systems such as ISO 13485 and 21CFR820, and have experience working with environmental management systems according to ISO 14001. You will work in a customer-oriented, international environment, so you must be fluent in both English and Swedish, both spoken and written. Personal Qualities You are responsible, well-organized, and business-minded with the ability to be driven and decisive when the situation requires it. You are a solution-oriented person who finds innovative solutions to both customer and internal challenges. You have a good ability to understand product complexity and have a holistic leadership perspective. To succeed in the job, it is important that you are thorough, have a structured approach to work, and are prepared to document your work carefully. You are an unpretentious team player who finds it easy to collaborate and communicate with others. Application Does the above description match you and do you feel this is an opportunity not to be missed? Then submit your application to [email protected] no later than 2026-09-13, but don't wait to apply as we work continuously with recruitment. For more information, contact Quality and Environmental Director; Martin Olin, 0734-021593, [email protected] HR Director; Stefan Hasselblad, 0768-617183, [email protected]

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