REQUIRED QUALIFICATIONS:

• Minimum 3 years of experience in a similar role within pharmaceutical GMP environments
• Strong expertise in GMP validation and complianceFluent in Swedish and English (both written and spoken)

ABOUT US

Medhouse is a consulting and recruitment company within Life Science. We have extensive experience and deep knowledge of the industry and are currently represented in all Nordic countries. We assist our clients with consulting and recruitment solutions within sales & marketing as well as in the medical & regulatory field.

ABOUT THE ROLE

As an Associate Director Validation, Site Quality, you will play a key role in ensuring compliance with GMP regulations and quality standards. You will contribute to maintaining quality oversight, driving continuous improvement, and setting the strategic direction for quality.

KEY RESPONSIBILITIES:

• Develop and maintain in-depth knowledge of quality regulations and guidelines
• Mentor and support junior colleagues
• Build strong customer relationships and engage in GxP audits and initiatives
• Develop and approve GMP documentation and QA risk assessments
• Provide Quality input into business improvement projects
• Participate in external Regulatory Authority GMP inspections
• Collaborate closely with leadership teams to shape quality strategies.