QA Labelling Specialist at Maurten

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About the job:

This position is a direct recruitment, meaning the recruitment process is conducted through Bravura, and you will be employed directly by Maurten.

About the company:

Maurten is an innovative company in the sports nutrition industry, focused on delivering scientifically advanced products to enhance athletic performance. With a dedicated team of researchers, nutritional experts, and athletes, they strive to create groundbreaking products fit for anyone who views themselves as an athlete. Their fundamental technology, based on hydrogel, has revolutionized the sports fuel category by enabling optimal conditions for carbohydrate absorption in the body, allowing athletes to maximize their energy levels and performance during training and competition. Maurten is committed to pushing the boundaries of sports nutrition by integrating scientific research, innovation, and quality into all products. They also value a culture of collaboration, passion for sports, and dedication to helping athletes achieve their goals at all levels. Founded in 2016, Maurten has experienced significant growth worldwide. Today, they operate globally, with employees in the US, UK, Canada and EU, and distributors managing sales in Japan, Australia, and South Africa. Today, Maurten consist of a global team of 68 passionate employees, where 40 of them are based at the HQ in Gothenburg, Sweden.

Tasks and responsibilities:

As a Labelling Specialist, you will be part of the Quality Assurance & Regulatory Affairs department, where your main task is to lead and create labelling design considering regulatory requirements in global markets. You will support business continuity and growth, reporting to the Head of Quality Assurance at Maurten. Your responsibilities include carefully mapping and managing the regulatory requirements for labelling and packaging in existing and future global markets. You will ensure that Maurten's packaging, labelling, and layout are compliant and meet all necessary requirements. Additionally, you will lead or participate in cross-functional projects and activities related to labelling, including contributing to design for manufacturability, ease of inspection, and cost optimization. You will provide strategic support to improve products for the market effectively. Developing processes within quality and regulatory requirements is a long-term focus area where you play a crucial role.

• Mapping of regulatory requirements in global markets
• Analysis and communication of solutions for internal labelling requirements
• Updating and maintenance of labelling-related documentation

Education, Experience and Personal characteristics:

• Engineering degree, preferably with a focus on quality
• Minimum 5 years of experience in labelling and regulatory work in global markets within Food, Pharma, or Medtech industries
• Fluent in English and proficient in Swedish
• Strong computer and system skills

To succeed in this role, we see that you are a structured person who plans your tasks carefully, always setting and adhering to timelines for your tasks and knowing what to prioritize. You pay attention to details and perform work thoroughly to ensure that everything is done with quality and precision. You enjoy working with multiple stakeholders internally and are not afraid to communicate decisions and inform about regulatory requirements to be followed. To thrive in Maurten's corporate culture and the growth journey they are on, we see that you enjoy working in a dynamic environment where you are open to changes and are flexible in decision-making processes and work methods.

Other information:

Start: Upon agreement
Location: Gothenburg
Salary level: Upon agreement

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