Bioprocess Engineer DSP

Lonza; Schweiz; Vor Ort; Vertraulich; Vollzeit

Benefits dieser Stelle

Agile career culture

Inclusive workplace

Competitive compensation programs

Lifestyle, family & leisure benefits

Visp local benefits information

Zusammenfassung

Lonza in Visp, Switzerland seeks a DSP Bioprocess Engineer to lead downstream processing campaigns and ensure compliant, safe, and efficient production of biopharmaceuticals. You will serve as a manufacturing subject matter expert and Functional Lead for assigned products, guiding teams through risk assessments, deviations, CAPAs and technology transfers.

The role emphasizes collaboration, regulatory readiness, and continuous improvement in a highly regulated environment.

Qualifikationen

• Experience in biopharmaceutical manufacturing with focus on downstream processing (DSP).
• Solid understanding of cGMP requirements and regulatory standards.
• Experience managing quality systems, risk assessments, deviations, CAPAs and change controls.
• Strong communication and leadership in cross-functional settings.

Aufgaben

• Lead DSP manufacturing campaigns, ensuring compliant execution, monitoring and documentation.
• Act as Functional Lead for assigned products, coordinating cross-functional teams.
• Drive risk management, including SHE, EM, operational and product risk assessments.
• Maintain GMP documentation and support audit readiness.
• Train manufacturing personnel and promote safety, quality and continuous improvement.
• Support capital projects, commissioning, qualification and tech transfers.

Kenntnisse

DSP manufacturing

cGMP compliance

risk assessments

project leadership

stakeholder management

cross-functional teams

Ausbildung

Biotech/Eng degree

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 DSP Bioprocess Engineer is responsible for the planning, execution, monitoring, and documentation of commercial and clinical manufacturing campaigns within the Downstream Processing (DSP) area. The role serves as the manufacturing subject matter expert for assigned products, ensuring compliant, safe, efficient, and reliable production according to cGMP requirements, regulatory expectations, and operational excellence standards. The DSP Bioprocess Engineer acts as the Functional Lead for manufacturing-related activities, supports plant operations, leads risk assessments and process improvements, and provides technical expertise for capital projects, commissioning, qualification, and operational readiness.

What you will do:

• Lead and oversee DSP manufacturing campaigns, ensuring execution, monitoring, troubleshooting, and documentation are compliant with cGMP and regulatory requirements.
• Act as the manufacturing Functional Lead for assigned products, coordinating cross-functional teams and maintaining technical expertise in processes, equipment, and facilities.
• Drive risk management activities, including SHE, EM, operational, cleaning, and product risk assessments, while supporting investigations, deviations, CAPAs, and change controls.
• Maintain GMP documentation such as SOPs, manufacturing instructions, risk assessments, and records to ensure compliance and audit readiness.
• Train and support manufacturing personnel, contributing to workforce development and fostering a culture of safety, quality, operational excellence, and continuous improvement.
• Represent manufacturing in capital projects, providing technical input for facility design, equipment selection, commissioning, qualification, and technology transfers.
• Lead continuous improvement initiatives and serve as a manufacturing representative during customer audits, inspections, and strategic cross-functional projects.

What we are looking for:

• Strong expertise in biopharmaceutical manufacturing, particularly downstream processing (DSP), with the ability to troubleshoot technical and process-related issues.
• Solid understanding of cGMP requirements and regulatory standards applicable to pharmaceutical manufacturing.
• Experience managing quality systems and compliance activities, including risk assessments, deviations, CAPAs, change controls, and validation.
• Proven problem-solving skills with the ability to identify root causes and implement effective corrective actions.
• Strong communication and stakeholder management capabilities, enabling effective collaboration across functions and organizational levels.
• Demonstrated project leadership and team coordination experience within complex, regulated manufacturing environments.
• Bachelor's or Master's degree in Biotechnology, Biochemical Engineering, Chemical Engineering, Life Sciences, or a related field, along with relevant experience in biopharmaceutical manufacturing, process engineering, technical operations, or cGMP-regulated environments.

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.