Biologics MS&T Manager: Lead Process Excellence (Uppsala)

Galderma Pharma S.A; Uppsala kommun; On-site; SEK 90,000 - 130,000; Full time

Job summary

Galderma is seeking an experienced Manager MS&T Biologics in Uppsala to lead a skilled team across biologics drug substance and drug product manufacturing. The role combines scientific depth with operational leadership to ensure product quality and regulatory compliance during commercial manufacturing.

You will drive lifecycle management, process validation, tech transfer, scale-up, and continuous improvement while collaborating with Regulatory Affairs, Quality, Engineering, and Supply Chain in

Qualifications

• Bachelor's or higher in biotechnology, chemical engineering, life sciences or related.
• Experience in pharmaceutical/biologics manufacturing with leadership responsibility.
• Strong knowledge of GMP-regulated environments and product lifecycle management.

Responsibilities

• Provide leadership and oversight for biologics drug substance and drug product manufacturing processes (fermentation, purification, formulation, aseptic processing, filling).
• Lead a team to support commercial manufacturing, troubleshoot, investigate deviations, and resolve process issues.
• Drive lifecycle management activities (validation, CPV, process optimization, tech transfers, scale-up) and ensure regulatory compliance.

Skills

Biologics manufacturing

Leadership

GMP knowledge

Fermentation

Process development

Tech Transfer

Regulatory knowledge

Cross-functional leadership

English

Swedish

Education

Bachelor's / Master's / PhD in Biotechnology or Life Sciences

Job description

Galderma is seeking an experienced Manager MS&T Biologics in Uppsala to lead a skilled team across biologics drug substance and drug product manufacturing. The role combines scientific depth with operational leadership to ensure product quality and regulatory compliance during commercial manufacturing.

You will drive lifecycle management, process validation, tech transfer, scale-up, and continuous improvement while collaborating with Regulatory Affairs, Quality, Engineering, and Supply Chain in