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Quality Assurance Project Manager
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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.
Further supporting our growth and innovation momentum, we are establishing a new Global Capability Center in Barcelona to deploy new capabilities to effectively support its global commercial and functional teams. Located in the upscale Eixample District in the heart of Barcelona, Galderma's Global Capability Center offers numerous possibilities for professional development such as exposure to global and cross-functional projects and access to global career opportunities.
Job Title: Quality Assurance Project Manager
Location: Hybrid, Barcelona
Job Description
Ensure Galderma products meet the Company quality standards and comply with the relevant government regulations according to the product applicable classification: cGMP, GDP, ISO, ICH or any relevant regulations and guidance.
Working under Galderma's CMO Oversight, the ideal candidate will be responsible for to ensure method transfer globally to different key partners. The candidate must possess in-depth knowledge of EU requirements, FDA regulations, and familiarity with other local regulations of major markets. The product in scope is a biologic, hence expertise in biologics manufacturing and quality assurance is essential
Key Responsibilities
Holding overall responsibility and ownership for the project results which includes strategy development, scoping, planning, execution, and budget/resource management, from initiation through implementation. Manage Analytical transfer or other specific projects to manufacturing sites Technical Transfer Lead Responsible for technology transfer activities at site level (within, inbound and outbound), including any scale-up or other process adaptations. Lead technical transfer project team at site and liaises efficiently with involved functions such external partners, Supply Chain, Production Unit, Quality Control, HSE, other sites.. Track and report progress across projects by reviewing schedules and due dates, identifying risks and assisting teams with contingency plans. Maintain accurate and up to date record of Project activities, including project status, risk & issues Prepare reporting to Managing Committees (Project Committees, Technical Review, Project Review Board, Interfaces, Highlights, etc.). Assess manufacturing capability & capacity as part of new supplier selection or existing supplier gap analysis activity. Ensure technical excellence in operational start-up for new manufacturing equipment and areas Assess and process supplier and company changes, ensuring product impact is appropriately considered. Supports CMO on technical activities during development and commercial manufacturing Skills & Qualifications
Bachelor's degree in Pharmacy, Biology, Biotechnology, Biochemistry, Chemistry, Engineering, Microbiology or another relevant scientific or engineering discipline; advanced degree is preferred. Six Sigma / Lean Manufacturing certification is a serious plus. At least 5 years of experience in a quality assurance role within the pharmaceutical or biopharmaceutical industry. Excellence operational knowledge of pharmaceutical manufacturing processes, including sterile production. Familiarity with regulatory requirements, including cGMP, FDA regulations, and international guidelines. Ability to work independently and collaboratively in a dynamic, fast-paced environment. Previous experience in leading or participating in regulatory inspections and audits. Excellent communication, problem-solving, and decision-making skills. Fluent in English What we offer in return
You will be working for an organization that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base. You will receive a competitive compensation package with bonus structure and extended benefit package You will be able to work in a hybrid work culture You will participate in feedback Loops, during which a personalized career path will be established You will be joining a growing company that believes in ownership from day one where everyone is empowered to grow and to take on accountability Process steps
Send your CV in English If your profile is a match, we will invite you for a first virtual conversation with Talent Acquisition The next step is a virtual conversation with the hiring manager The final step is a panel conversation with the extended team Our people make a difference
At Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.
