We are partnering with a leading pharmaceutical organisation that is shaping the future of pioneering therapies. They are seeking a motivated and experienced Qualification Engineer to join their growing team in Visp and contribute to the success of their high-impact production operations.

This Will Offer You

• A high-impact role within a mission-led organisation focused on patients, people, and the planet.
• Opportunity to be part of the set up of plant and the growth opportunity this offers
• Opportunities to work alongside and learn from highly experienced professionals.
• A collaborative culture that values learning, development, and continuous improvement.
• A competitive package including a strong pension plan, annual bonus, and additional financial and non-financial benefits.

Your Responsibilities

• Lead the qualification of facilities, utilities, and manufacturing systems in line with GMP standards.
• Independently plan, execute, or supervise DQ-IQ-OQ-PQ qualification activities, including FATs and SATs.
• Drive the evolution of the site’s qualification strategy in alignment with current regulations and technical advances.
• Take ownership of new qualification projects from initiation to completion.
• Represent the qualification function in audits and regulatory inspections.

You Will Need

• At least 5 years of experience in qualification within GMP-regulated or medical device environments.
• A technical background, either via vocational training and engineering certification or a relevant technical/scientific degree.
• Strong written and verbal communication skills in English; German is a plus.
• A flexible mindset and ability to thrive in a dynamic, fast-paced setting.
• Experience in aseptic manufacturing or fill-finish processes is highly advantageous.