• Manage supplier control and supplier management.
• Plan and perform quality audits of suppliers, service providers and contract manufacturers.
• Analyse audit data and identify deviations from GMP/GDP and follow up on audit observations.
• Manage supplier change notifications.
• Manage deviations in relation to materials and services.
• Manage quality agreements.
• Research and evaluate QA policies, deploying strategies for improved effectiveness.
• Analyze ongoing QA processes and identify areas for improvement.
• Establish relationships with internal and external stakeholders, advising and guiding on QA matters.

• Bachelor's/master’s degree within a relevant field.
• Documented experience working with GMP within medical devices (ISO 13485) and/or pharmaceuticals is required.
• Professional level in Swedish and English
• Experience from quality or regulatory in a regulated environment is an advantage.
• Experience with supplier management is an advantage.
• Experience from laboratory work is an advantage.

• If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
• The next step is an interview with the hiring manager and the extended team.