Manager MSAT Device Injectables

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 bodys 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.

Job Title: Manager MSAT Device Injectables

Location: Uppsala Sweden (Hybrid)

We are looking for a passionate and strategic Manager Devices and Injectables to join our world-class MS&T organization in Uppsala. This is a unique opportunity to lead the technical strategy process excellence and lifecycle management for Galdermas most advanced injectable and device products shaping global launches driving innovation and ensuring manufacturing performance that impacts millions of patients worldwide.

At Galderma you wont just take on a job youll contribute to science-driven solutions guide a high-performing team and build the next generation of manufacturing capability. If youre ready to combine leadership with meaningful impact this is the role for you.

About Galderma

Galderma is the emerging pure-play dermatology category leader present in approximately 90 countries. We deliver an innovative science-based portfolio of flagship brands and services across Injectable Aesthetics Dermatological Skincare and Therapeutic Dermatology.

Since 1981 we have dedicated our focus and passion to the human bodys largest organ the skin. By understanding that the skin we are in shapes our lives we are advancing dermatology for every skin story.

Job Description

As Manager Devices and Injectables you will lead the technical lifecycle management of Devices and Injectables and act as a key driver for robust manufacturing processes. You will serve as a technical authority ensure compliance with global regulatory expectations and lead a team of MS&T specialists dedicated to injectable and device manufacturing.

Your focus will span process validation tech transfer CPV troubleshooting investigations and continuous improvement forming the backbone of safe high-quality and efficient production.

Key Responsibilities

As the Manager Devices and Injectables you will drive technical strategy and operational excellence across manufacturing processes. Acting as a technical authority you will ensure products are manufactured safely efficiently and in full compliance with global standards.

You will lead and support new product introductions major technology transfer activities and product remediation initiatives while ensuring process knowledge is maintained and continuously improved. A core part of your role is to assess the impact of manufacturing changes define and track technical CAPAs and provide MS&T expertise during deviations investigations and technical complaints.

You will develop and execute process validation and revalidation strategies author and review protocols and reports and oversee ongoing continued process verification and annual product reviews. Your analyses will feed into recommendations for corrective actions and long-term improvements.

Collaboration is central: you will work closely with Production Quality Engineering R&D and global partners to resolve shop-floor challenges support change controls lead risk assessments and provide technical insight during supplier evaluations.

As a people leader you will mentor and develop MS&T scientists fostering an inclusive collaborative environment where expertise grows and accountability thrives. You ensure operational continuity by delegating effectively and building a resilient high-performing team.

Key Requirements & Qualifications

To succeed in this role you bring a strong mix of technical depth leadership capability and regulatory understanding within pharmaceutical and medical device manufacturing particularly in Devices and Injectables. You are comfortable navigating a global environment and balancing strategic decision-making with hands-on technical support.

You likely have 10 years of experience in pharma or medical device manufacturing ideally with exposure to Devices and Injectables fill-finish or related processes and at least 3 years of managerial experience guiding technical experts or cross-functional teams.

Your background includes a solid foundation in manufacturing science and technology experience in technology transfer and a strong track record in process validation (PPQ CPV) and lifecycle management. You are well-versed in GMP ISO 13485 ICH and global regulatory expectations and have led investigations performed root-cause analyses implemented CAPAs and contributed to regulatory submissions (IND BLA NDA or variations).

Core competencies include:

• Leading technology transfers from development to commercial manufacturing
• Designing executing and reviewing process validation and revalidation protocols
• Managing deviation investigations and implementing CAPAs
• Supporting regulatory submissions and compliance inspections
• Collaborating across matrix and international teams

Strong communication skills the ability to explain complex technical topics to diverse stakeholders and fluency in English are essential.

Additional strengths that are highly beneficial include experience with structured problem-solving tools (FMEA Ishikawa 5 Whys) global or cross-border technology transfers project management certifications (PMP PRINCE2) and Swedish language skills.

Why Join Galderma in Uppsala

Our Uppsala site is Galdermas Global Center of Excellence for Aesthetics home to over 800 professionals across R&D manufacturing engineering and clinical development. Here science meets real-world application and innovation becomes product reality.

What we offer

• Career development & learning opportunities
• Attractive benefits and bonus programs
• High-impact Devices and Injectables projects
• A global & inclusive culture
• Strong team spirit and engagement
• Work-life balance & wellbeing initiatives

Are You the One Were Looking For

We seek people who take ownership drive results embrace learning and bring positive energy to their teams. You combine initiative with collaboration and are motivated by contributing to something that truly matters for patients consumers and healthcare professionals.

At Galderma we empower employees develop strengths and celebrate diversity. Here you will grow your career expand your expertise and make a meaningful difference.