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Marketing labeling manager to the Medtech industry in Gothenburg jobb i Göteborg på Randstad AB

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Marketing labeling manager to the Medtech industry in Gothenburg på Randstad AB

Marketing labeling manager to the Medtech industry in Gothenburg

Randstad AB Göteborg, Västra Götalands län Deltid


job description.

For consultant assignments within the Medtech industry, we are now looking for a Labeling manager with experience of medical devices. As responsible for labeling of products, you will lead and coordinate the introduction of new and changed information affecting the labeling and Instructions for use. This role requires a structured hands-on approach for ensuring the information and symbols are according to regulations and understandable to users and healthcare professionals. You will also be involved in new product development projects and play an active role when entering new markets. All aspects of this role require active collaboration with all company functions, our commercial entities around the world as well as other external stakeholders such as advertising agencies and translation providers.

Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.



responsibilities.

Your work tasks may include:

• Plan, lead and prioritize activities to develop new or change the product labeling including instructions for use while closely collaborating cross-functionally with relevant stakeholders.
• Coordination between HQ and our commercial entities around the world regarding product and labeling changes and understand the market and business effects of such changes.
• As the key stakeholder and labeling responsible, you will participate in product development projects to ensure compliance with relevant regulations and understandable instructions.



working hours.

Full time for 3 months, might be prolonged. Start in the middle of august. 


qualifications.

The job requires flexibility, self-motivation and professional ethics. To fit the role you are enthusiastic about generating correct information, you are structured and have a patient disposition. You hold a B.Sc. in biology, biotechnology or similar field. You have 2-5 years of experience in medical device or other highly regulated industry. 
For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.

You have experience in areas such as Medical Device Regulation (MDR) and Quality Management System for medical devices, ISO 20417.



application.

2021-08-06, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.
For more information, please contact Linda Inge [ Email address blocked ]

 

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Job ID: 201351866