Senior CSV Engineer

<p><span><span>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.</span></span></p><p><span><span> </span></span></p><p><span><span>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.</span></span></p><p><span><span> </span></span></p><p><span><span>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.</span></span></p><p>CSV Engineer</p><p></p><p>Do you enjoy making sure systems work as they should and want to contribute to high-quality, compliant solutions?</p><p>At Galderma, we’re growing our engineering team in Uppsala and are looking for a Computerized System Validation (CSV) Engineer to support both daily operations and long-term projects. With new systems being implemented and existing ones evolving, you’ll have the opportunity to join us at a time of exciting development and change, with the opportunity to contribute from the start. Galderma is the world’s largest independent dermatology company, offering a science-based portfolio across aesthetics, skincare, and therapeutic solutions in close collaboration with healthcare professionals.</p><h3></h3><h3><b>The role</b></h3><p>You’ll be part of a collaborative engineering team that works closely with colleagues in automation, commissioning, qualification, and quality. The team ensures that hardware installations, software validation, and data management are all compliant, reliable, and well-documented. As a CSV Engineer, your focus will be on the validation and qualification of computerized systems connected to Facility, Utility, and Manufacturing areas. You’ll ensure systems are implemented correctly, perform as intended, and meet the relevant regulatory requirements such as GxP and GAMP5.</p><p></p><p><b>In this role, you will:</b></p><ul><li>Function as the SME (subject matter expert) regarding Computerized System Validation and provide guidance to engineers within the organizaition and project teams.</li><li>Plan, write, and execute validation protocols (IQ, OQ, PQ) for computerized systems</li><li>Review system design and functionality to ensure compliance with regulatory requirements and industry standards.</li><li>Perform hands-on testing of systems and interfaces</li><li>Ensure that all OT systems and processes meet, and can be used as intended, according to the required standards and regulations.</li></ul><p></p><h3><b>Who are you?</b></h3><p>To thrive as a CSV Engineer at Galderma, you’re someone who values collaboration and enjoys being part of a team working toward shared goals. You bring a positive mindset, are flexible in how you work, and take a structured approach to tasks. You're naturally curious about how systems operate, especially within Operational Technology (OT), and you like making sure they run smoothly, communicate correctly, and meet all the right standards.</p><p></p><p><b>We believe you also bring: </b></p><ul><li>At least 5 years of experience with Computerized System Validation (CSV), ideally from the pharmaceutical or medical device industry, where quality and compliance are part of everyday life.</li><li>Familiarity with GxP environments and frameworks like GAMP5</li><li>Experience creating and executing Plans, Protocols, Test Scripts and Reports as they relate to Qualification and Validation of assigned Computerized systems associated with Facility, Utility and Manufacturing GxP systems throughout their lifecycle.</li><li>Proficency with all the phases of SDLC (System Development Life Cycle), STLC (system testing life cycl) processes, Validation methologies and Concepts of Qualification Documents/ Protocols.</li><li>Fluency in both Swedish and English  </li></ul><p></p><p><b>What we