Drug Product

Vor 6 Tagen

Visp, Schweiz Experis Vollzeit

**​** 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.

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