Technical Lead, Sterile Products — Barcelona (MS&T)

Galderma; Bellprat; Presencial; EUR 90.000 - 110.000; Jornada completa

Descripción de la vacante

Galderma in Barcelona is seeking a Technical Lead specialized in sterile products to join the External Supply Organization. You will act as the technical expert for sterile manufacturing, lead tech transfers, and drive lifecycle management from development to commercialization.

The ideal candidate holds a Master’s degree in Pharmaceutical Technology or related field, 8–12 years in MS&T with sterile products in GMP environments, and fluent English.

Formación

• Master's degree in Pharmaceutical Technology, Biochemistry, Chemical Engineering, Life Sciences, or a related field.
• 8–12 years of experience in Manufacturing Science and Technology with sterile products in a GMP environment.
• Experience in aseptic processing, validation, tech transfer, lifecycle management, and dev-to-commercialization.

Responsabilidades

• Serve as the technical subject matter expert for sterile manufacturing processes and products.
• Provide technical stewardship for commercial products and support NPI at CMOs.
• Lead lifecycle management activities including process, raw material, and packaging changes.
• Drive process improvements focused on quality, yield, efficiency and cost.
• Support technology transfers for sterile products, injectable semi-finished products, and medical device assembly.
• Lead investigations, troubleshooting and risk assessments related to deviations.
• Collaborate with internal and external partners to ensure knowledge sharing and execution.
• Review and approve manufacturing specifications, protocols, and reports.

Conocimientos

Sterile manufacturing

GMP compliance

Process troubleshooting

Cross-functional collaboration

Project leadership

Technical documentation

Educación

Master's degree in Pharmaceutical Technology

Descripción del empleo

Galderma in Barcelona is seeking a Technical Lead specialized in sterile products to join the External Supply Organization. You will act as the technical expert for sterile manufacturing, lead tech transfers, and drive lifecycle management from development to commercialization.

The ideal candidate holds a Master’s degree in Pharmaceutical Technology or related field, 8–12 years in MS&T with sterile products in GMP environments, and fluent English.