Quality Control Specialist

At Galderma, we are driven by innovation, quality, and a shared commitment to improve patients' lives. We are now looking for an experienced Quality Control Specialist to strengthen our Quality Control organization and ensure robust, compliant, and continuously improving QC processes.

In this role, you will take ownership of QC quality activities, act as a subject matter expert, and collaborate closely with cross-functional stakeholders to support product quality, regulatory compliance, and operational excellence.

Your Responsibilities

• Ensure QC activities are performed in compliance with GMP, internal procedures, and applicable regulatory requirements
• Identify, assess, and mitigate quality risks within QC processes
• Lead and support deviation investigations, change controls, and corrective actions
• Perform QC release and final acceptance according to certification and delegation
• Support and coordinate audits, inspections, and regulatory interactions
• Drive continuous improvements using systematic tools such as QRM and/or Yellow Belt methodologies
• Train and support QC managers and employees in cGMP and QC-related requirements
• Act as a trusted QC subject matter expert, providing guidance and technical leadership

Skills & Competencies

• Strong understanding of QC processes and quality systems in regulated environments
• Proven ability to work independently while managing complex and sometimes ambiguous issues
• Structured, analytical, and risk-based mindset
• Strong problem-solving and decision-making skills
• Ability to influence and guide stakeholders without direct authority
• Clear and professional communication skills, both written and verbal
• Collaborative mindset with the ability to build strong cross-functional relationships
• Continuous improvement mindset with experience driving change

Your Profile

• Bachelor's degree in a relevant scientific field or equivalent experience
• 5-8 years of experience within Quality Control in a regulated pharmaceutical and/or medical device environment
• Strong knowledge of GxP and relevant regulations (ISO 13485, EudraLex Volume 4, 21 CFR Parts 11, 211, and 820)
• Experience with QC release, final acceptance, and incoming material release
• Fluent Swedish is a must. Professional working proficiency in English is required.