​
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.
​
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.