| Location | Visp, - None Specified - |
|---|---|
| Business Sector | Pharmaceutical |
| Contact email | |
| Job ref | 26115 |
| Published | about 2 hours ago |
Project Champion – Drug Product Manufacturing | Life Sciences | GMP, Capacity Expansion & Technical Projects
A global leader in the Life Sciences industry, this organization focuses on advancing drug manufacturing through innovation, technical excellence, and collaboration. With operations spanning multiple continents, the company is committed to improving human health by enabling efficient and compliant production environments. Employees are empowered to take ownership of their work, contribute to high-impact projects, and grow professionally within a culture of continuous improvement.
As a Project Champion – Drug Product Manufacturing, you will lead technical expansion and capacity increase projects to support production ramp-up activities. You will provide critical technical input to project design, ensuring compliance with operational requirements and regulatory standards (including EU GMP Annex 1). This role requires strong project governance, collaboration with cross-functional teams, and the ability to drive projects to completion on time and within scope.
You will also play a key role in implementing best practices, managing change controls, and supporting deviation and troubleshooting activities, ensuring that manufacturing processes and equipment align with cGMP standards.
Lead and execute technical expansion and capacity increase projects within Drug Product manufacturing.
Provide technical input to project design, ensuring compliance with GMP and regulatory standards (e.g., EU GMP Annex 1).
Coordinate cross-functional teams and external suppliers to achieve project objectives.
Manage project governance and ensure timely delivery within defined scope and quality standards.
Develop and implement best-practice processes aligned with industry and regulatory expectations.
Manage change control, troubleshooting, and deviations related to projects and equipment.
Collaborate with manufacturing and quality teams to establish and maintain operational procedures.
Minimum of 2 years’ experience in a GMP-regulated manufacturing environment (Drug Product experience preferred).
Proven track record in project coordination or project management within pharmaceutical manufacturing.
Experience with CAPEX projects and equipment qualification is an advantage.
Strong understanding of cGMP principles and Annex 1 requirements.
Fluent in English; German is an asset.
Excellent interpersonal and communication skills; highly collaborative and results-driven.
Agile mindset with the ability to perform under pressure and manage shifting priorities.
On-site role – no home-office option.
Location: Visp, switzerland
Department: Drug Product Manufacturing / Engineering
Work Type: On-site
Interested? Please send your CV to Miguel Gomes at m.gomes@panda-int.com or reach out directly at +31 20 20 44 502.