Quality Control Specialist

Om jobbet

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.

We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.

At Galderma, we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.

Quality Control Specialist

AtGalderma, we are driven by innovation, quality, and a shared commitment to improve patients' lives. We are now looking for an experiencedQuality Control Specialistto 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.