Manufacturing Scientist, Assembly & Packaging

Galderma; Uppsala kommun; On-site; SEK 700,000 - 900,000; Full time

Job summary

Galderma seeks a Senior Manufacturing Scientist for the Uppsala MS&T team. You will provide technical oversight for assembly and packaging, drive process improvements, and lead complex investigations.

You will analyze data, collaborate across functions, and support regulatory inspections to ensure GMP-compliant manufacturing. Ideal candidates hold a 6–10 year track record in biopharma/manufacturing, with strong analytical skills and experience in validation, DOE/Six Sigma, and quality systems.

Qualifications

• Bachelor's/Master's/PhD in chemistry or related field.
• Experience in biopharma, medical devices, or manufacturing (6–10 years).
• Strong investigations and root cause analysis capabilities.
• Knowledge of GMP/regulatory frameworks and quality systems.
• Excellent communication and stakeholder management.

Responsibilities

• Provide technical oversight for assembly and packaging processes.
• Drive continuous improvement to enhance robustness and quality.
• Lead investigations, root cause analyses, and CAPA implementation.
• Analyze manufacturing data to identify trends and risks.
• Collaborate cross-functionally to resolve technical challenges and ensure GMP compliance.
• Support regulatory inspections and validation activities.

Skills

Root cause analysis

Investigations

Data analysis

Stakeholder management

Problem solving

Documentation

GMP/compliance knowledge

Cross-functional collaboration

Education

Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or related field

Tools

JMP

Minitab

Python

R

Power BI

Spotfire

MES

LIMS

ERP

SCADA

Job description

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.At Galderma, we advance dermatology for every skin story. As the pure-play dermatology category leader, we combine innovation, science, and manufacturing excellence to deliver solutions that improve the lives of patients worldwide.We are now looking for a Senior Manufacturing Scientist to join our Manufacturing Science & Technology (MS&T) team in Uppsala. In this role, you will serve as a key technical expert supporting assembly and packaging operations, driving process performance, product quality, and continuous improvement through scientific expertise and data-driven decision-making.The RoleAs a Senior Manufacturing Scientist, you will provide technical oversight and process support for commercial manufacturing activities while partnering closely with production, quality, engineering, validation, and supply chain teams. You will play a central role in investigations, process optimization initiatives, and the application of analytical tools to improve operational excellence.Key ResponsibilitiesProvide scientific and technical support for assembly and packaging processes.Drive continuous improvement initiatives to enhance process robustness, efficiency, and product quality.Lead and support complex investigations, root cause analyses, and implementation of effective corrective and preventive actions.Analyze manufacturing and quality data to identify trends, risks, and opportunities for improvement.Apply statistical and analytical methodologies to support process understanding and optimization.Collaborate cross-functionally to resolve technical challenges and ensure reliable manufacturing operations.Support regulatory inspections, audits, and compliance activities.Ensure manufacturing processes operate in accordance with GMP requirements and applicable regulatory expectations.Contribute technical expertise to validation, risk assessments, and change management activities.Who You AreYou combine strong scientific knowledge with a practical manufacturing mindset. You enjoy solving complex technical problems, working with data, and influencing stakeholders across functions to deliver sustainable improvements.QualificationsBachelor's, Master's, or PhD degree in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or another relevant scientific or engineering discipline.Approximately 6-10 years of experience within biopharmaceutical, medical device, or manufacturing environments.Strong experience in investigations, root cause analysis, and structured problem-solving methodologies.Excellent analytical skills, including data collection, interpretation, and reporting.Knowledge of cGMP requirements and regulatory frameworks.Experience supporting inspections and regulatory audits.Strong communication, documentation, and stakeholder management skills.Technical ExpertiseAssembly and packaging processes and manufacturing equipment.Data analysis tools such as JMP, Minitab, Python, R, Power BI, or Spotfire.Manufacturing systems including MES, LIMS, ERP, and SCADA.Statistical and quality methodologies such as SPC, DOE, and Six Sigma.GMP regulations and guidelines, including FDA, EMA, ICH, and Annex 1 requirements.Validation principles, risk assessment, and quality-by-design approaches.Preferred QualificationsSix Sigma Green Belt or Black Belt certification.Experience with digital validation systems and advanced analytics platforms.Experience working in multi-site manufacturing organizations or CMO environments.Why Join Galderma?This is an opportunity to take on a highly visible role where science, manufacturing, and innovation come together. You will work in a collaborative environment alongside experienced colleagues while helping shape the future of manufacturing excellence at Galderma's Uppsala site.Join us and contribute to delivering high-quality products that make a meaningful difference for patients around the world.