QC Specialist Analytical Methods

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.

Location: Uppsala

Employment type: Full-time

Join Galderma, a leading global dermatology company with a strong international presence and a commitment to innovation, collaboration, and excellence. We offer exciting opportunities for personal and professional development in a dynamic and purpose-driven environment.

The Role

We are seeking a Quality Control Specialist - Analytical Methods to join our Quality Control (QC) organization. In this expert-level role, you will act as the technical authority for analytical methods, providing scientific guidance, training, and support to QC colleagues, other departments, and Galderma's global network. You will ensure analytical methods and laboratory practices meet regulatory and internal quality standards, lead method validations, and drive continuous improvement and optimization within the analytical area. This role offers an exciting opportunity for a seasoned professional who enjoys solving complex challenges and influencing quality and compliance on a global scale.

Key Responsibilities

• Serve as Subject Matter Expert (SME) in analytical chemistry, with deep expertise in chromatographic techniques (e.g., HPLC, GC), including troubleshooting, method development, and validation.
• Provide technical leadership, coaching, and support to QC teams and cross-functional colleagues.
• Lead and coordinate method validations, including planning, execution, data evaluation, and authoring of validation reports.
• Ensure that analytical methods and QC operations comply with GMP and GxP requirements and Galderma standards.
• Identify, evaluate, and mitigate quality and compliance risks; contribute to deviation investigations with advanced technical insight.
• Represent QC in cross-functional and global projects, contributing expert knowledge and analytical perspective.
• Drive improvement initiatives using structured methodologies such as Quality Risk Management (QRM) and Lean/Yellow Belt tools.
• Prepare and present technical documentation, reports, and presentations for internal and external stakeholders, including auditors and regulatory authorities.
• Contribute actively to a positive, collaborative, and compliant laboratory culture.

Your Profile

• PhD or Master's degree (or equivalent) in Chemistry, Pharmaceutical Science, or a related field.

Experience:

• Minimum 10 years of experience in Quality Control or R&D, focusing on analytical method development and validation.
• Extensive experience with chromatographic methods and advanced analytical instrumentation.
• Proven understanding of GxP, GMP, and pharmaceutical and/or medical device regulations.
• Demonstrated ability to train, coach, and communicate technical concepts clearly to diverse audiences.

Skills:

• Strong analytical, problem-solving, and project management skills.
• Excellent communication and presentation abilities in Swedish and English (both written and spoken).
• Ability to work independently and collaboratively across teams and geographies.