Quality Control Specialist Microbiological methods

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. Location: Uppsala Employment type: Full-time The Role We are seeking a Quality Control Specialist – Microbiological Methods to join our Quality Control (QC) organization. In this senior expert role, you will act as the technical authority for microbiological analytical methods, providing scientific guidance, training, and support to QC colleagues, cross-functional departments, and Galderma’s global network. You will ensure analytical methods and laboratory routines comply with GMP and internal quality standards, lead method validations, and drive continuous improvement within the microbiological area. This position is ideal for an experienced professional with advanced technical expertise and a passion for quality, science, and innovation. Key Responsibilities Serve as Subject Matter Expert (SME) in microbiological methods, including troubleshooting, optimization, and method development. Provide technical leadership, guidance, and mentorship to QC team members and cross-functional stakeholders. Lead and coordinate microbiological method validations, including design, execution, evaluation, and report writing. Ensure microbiological analyses and QC operations comply with GMP, GxP, and Galderma quality standards. Identify, evaluate, and mitigate quality and compliance risks; contribute technical expertise to deviation investigations. Represent QC in cross-functional and global projects, contributing microbiological insights and expertise. Drive continuous improvement and simplification of analytical methods, work instructions, and quality systems. Prepare and present technical documentation, reports, and presentations for audits, inspections, and management reviews. Promote and contribute to a positive, compliant, and collaborative laboratory culture. Your Profile Education: PhD or Master’s degree (or equivalent) in Microbiology, Biotechnology, Biochemistry, or a related field. Experience: At least 10 years of experience in Quality Control or R&D, with strong focus on microbiological methods and method validation. Extensive laboratory experience in microbiological techniques, including troubleshooting and optimization. Documented experience with GxP, GMP, and regulatory frameworks relevant to pharmaceuticals and/or medical devices. Proven ability to train, coach, and communicate complex technical information clearly and effectively to diverse audiences. Skills: Advanced problem-solving and analytical thinking skills. Strong communication and presentation abilities in Swedish and English (both written and spoken). Ability to manage complex projects independently and work collaboratively across functions and geographies. Proactive and structured approach to process design, improvement, and quality risk management.