MSAT Process Specialist

Lonza Group Ltd.; Oberwallis; Vor Ort; CHF 110.000 - 160.000; Vollzeit

Benefits dieser Stelle

Agile career culture

Inclusive workplace

Competitive compensation

Lifestyle and family benefits

On-site Visp benefits

Zusammenfassung

Lonza is seeking a MSAT Process Specialist for the Visp site to support transfer, scale-up and validation of biopharmaceutical manufacturing processes. You will provide hands-on technical expertise to ensure robust production.

You will collaborate with Manufacturing, QA, Engineering and R&D, develop validation protocols, SOPs, and reports, and help drive continuous improvement while maintaining cGMP compliance at a fast-paced site.

Qualifikationen

• Degree in Chemical Engineering, Biotechnology, Biochemistry or related field.
• 3–5 years' experience in biopharma process development, MSAT or manufacturing support.
• Strong knowledge of downstream purification processes and cGMP.
• Experience with technology transfer, scale-up and validation activities.
• Proficient data analysis and problem-solving skills.

Aufgaben

• Lead/process validation activities in downstream unit operations.
• Support transfer of new manufacturing processes from R&D to production with scale-up and validation.
• Investigate deviations, perform CAPAs and root-cause analysis.
• Develop and revise process documentation, SOPs, protocols, and reports.
• Provide technical support to manufacturing and collaborate with cross-functional teams.
• Support regulatory submissions and data trending for process performance.

Kenntnisse

Process development

MSAT

Manufacturing support

Data analysis

Problem solving

English communication

Ausbildung

Bachelor's or Master's degree in Chemical Engineering/Biotechnology/Biochemistry

Jobbeschreibung

The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards

What you'll get:

• An agile career and a dynamic work culture
• An inclusive and ethical workplace
• Compensation programs that recognize high performance
• In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits.
• The full list of our local tailored benefits can also be found below
• Benefits in Visp: https://bit.ly/3wjkoFi

The MSAT Process Specialist of DSP at Lonza AG will play a key role in supporting the successful transfer, scale-up, validation activities, continuous improvement of biopharmaceutical manufacturing processes. This individual will provide technical expertise and hands-on support to ensure robust and efficient production.

What you will do:

• Execute and oversee process validation activities in downstream unit operations.
• Support the transfer of new manufacturing processes from R&D to manufacturing, ensuring successful scale-up and validation activities
• Support root cause analysis for process deviations and implement effective corrective and preventive actions (CAPAs).
• Develop and revise process documentation, including process description, validation protocols and reports, standard operating procedures (SOPs), and technical reports.
• Provide technical support to manufacturing operations for troubleshooting and continuous process improvement initiatives.
• Collaborate with cross-functional teams including Manufacturing, Quality, Engineering, and R&D.
• Support regulatory submissions.
• Conduct data analysis and trending to monitor process performance and identify areas for improvement.

What we are looking for:

• Bachelor's or Master's degree in Chemical Engineering, Biotechnology, Biochemistry, or a related scientific discipline.
• Minimum of 3-5 years of experience in process development, MSAT, or manufacturing support within the biopharmaceutical industry.
• Strong understanding of downstream (purification) manufacturing processes.
• Experience with process scale-up, technology transfer, and validation activities.
• Proficiency in data analysis and statistical tools.
• Excellent problem-solving skills and a strong analytical mindset.
• Ability to work effectively in a fast-paced, team-oriented environment.
• Strong written and verbal communication skills in English.
• Knowledge of cGMP regulations and quality systems.

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences?

Every day, our teams across the world work together to turn scientific breakthroughs into life-changing medicines that reach up to 100 million patients a year. Lonza is a place where people can make a unique impact, grow their careers and belong.

You will feel at home at Lonza if you:

• Take ownership, step forward, and enjoy meaningful responsibility
• Love solving problems and thrive in a complex, fast-moving environment
• Are curious, always looking to learn and improve
• Work collaboratively, contributing to something bigger than yourself
• Are motivated to make a difference through work that impacts customers and their patients

Why Lonza:

We are a place of unique opportunity, where your ideas, expertise and ambition can make a real difference. Here, will have the freedom to grow, the support to succeed and the chance to contribute to work that matters. We are the makers of the medicines of tomorrow. Join us. Be you.