Beschreibung

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Join a leading global pharmaceutical company dedicated to improving patient outcomes through innovative drug development and manufacturing. Renowned for its commitment to quality, sustainability, and cutting-edge technology, this organization offers a dynamic and collaborative environment where your expertise can make a meaningful impact. Located in the picturesque region of Visp, Switzerland, the company provides an inspiring setting for professional growth and development within the pharmaceutical industry.
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Description:
Key responsibilities:
- Lead technical expansion and capacity increase projects within Drug Product manufacturing to support production ramp-up.
- Provide technical input to project design, ensuring compliance with operational needs and regulatory standards (e.g., EU GMP Annex 1).
- Coordinate cross-functional teams and external suppliers, manage project governance, and ensure delivery on time and within scope.
- Develop and implement best-practice processes aligned with current industry and regulatory trends.
- Manage change control, troubleshooting, and deviations related to projects and equipment.
- Establish and update operational procedures in collaboration with manufacturing and quality functions.


Key requirements:
- Extensive technical experience in GMP manufacturing (Drug Product experience preferred).
- Proven track record of project coordination/management within pharmaceutical manufacturing.
- Experience with CAPEX projects and equipment qualification is an advantage.
- In-depth knowledge of cGMP and Annex 1 requirements.
- Fluent in English, german is a plus
- Highly collaborative, results-driven, and with excellent interpersonal and communication skills.
- Agile mindset with ability to deliver under pressure and changing priorities.

- min. 2 years experience
- no home-office**​**
If you believe you are the perfect fit for the role and you are interested, do not hesitate to call or email me directly.