Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

Based in Visp , Switzerland, we are looking for an experienced and driven Senior Manager, Growth Projects - Advanced Synthesis. In this key role, you will lead the execution of internal improvement projects for strategic growth CAPEX projects across our global network, ensuring lean, efficient, and scalable delivery. As part of the Systems and Process Improvement team, you will work closely with Global Engineering, Operations, MSAT and Quality.

You will directly support the Director of Operations in transforming project execution practices, contributing to the long-term success and operational excellence of our Advanced Synthesis platform.

Relocation assistance is available for eligible candidates and their families, if needed.

Key Responsibilities

Lead the development and implementation of lean, scalable, and harmonized processes for strategic CAPEX project execution and operational readiness. Optimize critical project activities, including lifecycle management, operator engagement, training, and commissioning/qualification/validation (CQV). Drive continuous improvement initiatives and integrate lessons learned and best practices into ongoing and future projects. Facilitate knowledge transfer and alignment across Advanced Synthesis sites. Contribute to the harmonization of plant and process design for small molecule and drug-linker manufacturing.

Key Requirements

Master's degree or equivalent experience in Engineering, Chemistry, Biologics, or a related scientific field with at least 5-10 years pharma proven experience. Extensive experience in cGMP chemical and/or biotechnological pharma engineering and manufacturing Demonstrated proficiency in handling complex projects. Proven ability to lead cross-functional teams in a matrix organization and drive operational improvements. Strong analytical and problem-solving skills with a proactive, change-oriented mindset. Fluency in English is required; proficiency in German is preferred. LBMS Green or Black Belt certification is a plus.

What you wil 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:

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

weniger ansehen

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

What you'll get:

An agile dynamic working culture An inclusive and ethical workplace Compensation programs that recognize high performance A variety of benefits dependent on role and location. The full list of our global benefits can be also found on Relocation assistance for eligible candidates and their families

What you'll do:

Ideation / Initiation Phase:

Assess and establish timelines, especially for customer-facing projects, with a focus on Probability of Success. Define and implement ORP governance, ensuring effective coordination within applicable workstreams and with relevant workstream owners. Lead Schedule workshops with workstream representatives to develop the overall End-to-End (E2E) timeline, identifying optimal time windows for each workstream. Challenge and validate proposed timelines, leveraging experience to recommend optimized approaches and time-saving strategies. Define key interface milestones between workstreams. Ensure all workstreams are integrated within the Capex schedule, as managed by the GE Project Control team. Facilitate schedule risk assessments and identify appropriate contingency measures.

Delivery Phase:

Further develop, monitor, and update the integrated project plans and IS to ensure project timelines reflect information from all workstreams, ensuring coordination and logical sequencing. Monitor schedule deviations, conduct root cause analysis, and develop corrective actions while escalating risks or roadblocks that could impact timelines. Proactively identify project risks and potential obstacles, collaborating with the E2E Lead to mitigate risks in a timely manner. Establish progress KPIs and reporting systems for each workstream, tracking performance against forecasts and targets. Prepare and provide regular IS progress reports, including comprehensive analysis. Facilitate project scheduling meetings and interactive planning sessions as required. Actively participate in Risk Meetings and contribute to the impact assessment of critical project areas. Regularly review schedules with project team members to ensure timely and accurate data is incorporated. Engage with workstream stakeholders and actively participate in daily reviews to drive project timelines, quality, and cost objectives; be the voice of maintaining a 'heartbeat' for on-target delivery

What we're looking for:

Proven experience in planning large-scale life sciences or food Capex projects from conception to manufacturing. Strong leadership and team management skills. Exceptional analytical capabilities with the ability to process large, complex data sets, draw actionable conclusions, and support decision-making processes. Demonstrated ability to work independently and collaboratively within team- oriented environments. Capable of navigating ambiguity and adjusting to shifting priorities and demands. Skilled at prioritizing and executing tasks in fast-paced, dynamic environments. Strong presentation, written, and oral communication skills. Preferable experience with Primavera P6 and Microsoft Project (though not essential)

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

weniger ansehen

The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

In order to support our continued growth Lonza is seeking Operators to join our talent community. Are you thinking about a career change? Become part of this exciting opportunity and join our outstanding team! Apply now as Operator BioConjugates!

What You'll get:

An agile career and a dynamic work culture

An inclusive and ethical workplace

Compensation programs that recognize high performance

A 6-week training program for career changer

What You'll Do:

Independent operation of familiar parts of the production plant in accordance with specification documents (manufacturing protocols / operating instructions / work instructions / SOP)

Safe and accurate execution of work in compliance with safety regulations and cGMP quality requirements

Responsibility for cleanliness and order in the workplace as well as the assigned rooms and warehouses

Every operator in the Ibex operation is involved as an equal team member through active assistance in continuous improvement processes

What we're looking for:

Vocational training (EFZ) or Education in Chemical, Biology or Pharmaceutical technology or proven experience

Meticulous and documentation skills

Carrying out work with a high level of safety awareness

Willingness to work in shifts (4-shift operation) with flexibility in work scheduling

Proficient in German and/or English

Knowledge of DeltaV or MES, as well as experience in GMP, is an asset

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

weniger ansehen

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

The Team Lead will oversee a team of 7-10 direct reports, providing strategic leadership and direction. This role is responsible for ensuring the effective execution and timely completion of site-wide hygiene-related projects that have a significant impact on the entire site's operations and performance.

Beyond team leadership, the Manager will drive program/project management activities, manage key stakeholder relationships, and serve as the primary liaison to senior management. The role also includes accountability for identifying, developing, and presenting continuous hygiene-related improvement initiatives to executive leadership, ensuring successful implementation and measurable business impact across the entire Visp site.

Join our team in Visp now! Relocation assistance is available for eligible candidates and their families , if needed.

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:

What you'll do:

Organizational & Leadership Duties

Lead and manage the assigned central hygiene team with directive authority

Oversee operational costs and ensure efficiency within the department

Shape strategic direction and contribute to projects and investment decisions

Create and maintain SOPs for hygiene and deviation processes

Ensure continuous training and development of team members, maintaining high standards of compliance and performance

Promote company vision, culture, and knowledge transfer across cross-functional teams

Hygiene Management

Oversees the planning, execution, and completion of site-wide hygiene-related projects with significant impact on Visp site operations and compliance.

Identify, propose, and execute innovative process improvements and cost-optimization initiatives, contributing to Lonza's strategic goals for operational excellence and financial performance.

Monitor industry trends, regulatory changes, and emerging best practices in contamination control and environmental monitoring, translating insights into actionable strategies for Lonza Visp.

Ensure execution of daily hygiene routines, such as the performance qualification (PQ) of cleanrooms

Audit Preparation & Participation

Represent deviation and hygiene processes in regulatory and customer audits in collaboration with the team.

Defend non-conformances and corrective actions during inspections

Serve as primary audit support for Hygiene related topics

Provide secondary audit support to QA Environmental Monitoring

Stakeholder Management

Act as the central contact for all hygiene-related matters, driving alignment and collaboration across Operations, Quality Control, Quality Assurance and other key stakeholders.

Influence and engage cross-functional stakeholders to build consensus and secure support for strategic hygiene initiatives, fostering a culture of continuous improvement and accountability.

What we re looking for:

Degree in Life Sciences, Engineering, or a comparable technical discipline

Extensive experience in deviation management and GMP-compliant hygiene programs, ideally within a complex manufacturing environment

Strong leadership and communication skills in a regulated, multicultural setting

Proven track record in successfully executing site-wide initiatives

Experience with regulatory and customer audits; strong stakeholder management capabilities

Strategic mindset paired with strong execution skills and a high sense of ownership

Fluent in English; German skills are an advantage

Analytical thinking, a structured working style and a strong commitment to quality complete your profile

At Lonza, our people are our greatest strength. Spread across 30+ sites and 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 shape what we achieve and how we achieve it. 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 offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

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Location: Stein (Switzerland)

Relocation assistance is available for eligible candidates and their families, if needed.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

Are you looking for a unique opportunity to integrate a Greenfield project (building several new production lines) into the existing manufacturing environment? As Head Quality CQV you will be part of the Site Quality Leadership team, shaping the quality landscape at Lonza AG in Stein!

What you'll get:

An agile career and dynamic working culture

An inclusive and ethical workplace

Compensation programs that recognize high performance

Along with competitive salaries, you'll find a wide range of lifestyle, family and leisure benefits available. The full list of our local benefits can be also found on assetstream.aspx

Key responsibilities:

Establish and maintain the Equipment Qualification System at Lonza Drug Product Services (DPS), including the commissioning, process and computerized systems validation, qualification of manufacturing equipment.

Lead and develop a team of QA Experts, guiding them in line with Lonza's values and behaviors, including objective setting, performance evaluations, development planning, and participation in the recruiting process. Support a culture of high performance and trust, ensuring the required level of knowledge and skills are available and identifying proficiency gaps

Ensure accurate qualification of equipment, infrastructure, and computerized systems by adhering to corresponding VMP(s). Support and ensure the implementation of global procedures related to CQV. Serve as the first contact for overarching documents related to equipment, infrastructure, and computerized systems qualification & maintenance within QA.

Supervise compliance activities such as GMP status and trending of equipment, qualification/re-qualification in relation to supplier qualification, changes, nonconformities, CAPAs, audit/inspection/self-inspection observations, and document management

Collaborate with other sites and global teams to improve and align CQV processes within Lonza. Ensure decisions are fully supported by global and local Quality and Regulatory standards

Ensure effective use of resources (budget, time, personnel, systems)

Coordinate the qualification of equipment suppliers/services by supervising adherence to quality agreements and audit observations. Track GMP status of service providers, including calibration, maintenance, and consultants

Key requirements:

Degree or equivalent experience in Life Science, Engineering, or a related field

Several years of leadership experience is a prerequisite

Work experience in Quality Assurance

Solid experience in qualification topics within the pharmaceutical, GMP-controlled sterile manufacturing area, including solid CQV experience is crucial

Experience with audits, including being part of the front office is a must; experience specifically with Swissmedic is an advantage

Demonstrated assertiveness to uphold quality standards and make decisive calls in fast-paced environments with opposing priorities

Proficiency in English is a must; language skills in German are a plus

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

weniger ansehen

Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist. Wir sind in der Wissenschaft tätig, jedoch gibt es keine Zauberformel dafür, wie wir die Arbeit angehen. Unsere wichtigste wissenschaftliche Lösung sind talentierte Mitarbeitende, die zusammenarbeiten und Ideen entwickeln, die anderen Unternehmen helfen, Menschen zu helfen. Im Gegenzug steuern unsere Mitarbeitenden ihre Karriere selbstständig. Denn ihre Ideen, ob gross und klein, verbessern die Welt. Und das ist die Art von Arbeit, an der wir Teil haben möchten.

Als Betriebs-/Anlagemeister (m/w/d) sind Sie zuständig für die technische und logistische Abwicklung von Produktionskampagnen in einem Produktionsbetrieb zur Herstellung von Biokonjugaten. Sie sind Mitglied eines interdisziplinären Teams und arbeiten in Projektteams mit, welche sich um Investitionen sowie Optimierungen von Abläufen, Tätigkeiten und Systemen kümmern.

Ihre Aufgaben:

Einbringung in Planungs- und Engineering Phase von Projekten, um technische Vorgaben für die Anlagen einzuhalten und eine erfolgreiche Produktionskampagne sicherzustellen

Organisatorische und betriebstechnische Betreuung, sowie Überwachung der Produktionskampagnen, zur Sicherstellung der Produktion und Sicherheit auch ausserhalb der normalen Arbeitszeit

Erstellung von cGMP gerechter Dokumentation in Zusammenarbeit mit dem Anlageteamleiter, der Forschung/Entwicklung und den Betriebsbiotechnologen

Anlagetechnische Instruktion und produktionsspezifische Ausbildung der Operatoren während der Produktion

Kontrolle der lückenlosen Befolgung der Betriebsvorschriften und Herstellungsprotokolle, sowie Eingriff bei Abweichungen

Unterstützung des Informationsaustausches und Kommunikation innerhalb der Betriebsgruppe

Durchgehende Verbesserung von Anlagen, Abläufen und Prozessen (6S, Lean Six Sigma, KAIZEN) unter Einhaltung der Sicherheits-, Hygiene-, Umwelt- und Qualitätsanforderungen

Ihr Anforderungsprofil:

Abgeschlossene technische Aus- oder Weiterbildung (Berufslehre, Höhere Fachprüfung, Bachelor, Master)

Vorteilhaft wäre Produktionserfahrung bei der Herstellung von chemischen oder biotechnologischen Produkten, oder in der Lebensmittelindustrie

Idealerweise erste Erfahrung im ISO- und / oder GMP-Produktionsumfeld

Sie verfügen über Grundkenntnisse in MS Office (Excel, Word) und sind affin für elektronische Systeme und Anwendungen

Sehr gute Deutschkenntnisse in Wort und Schrift, sowie Englischkenntnisse

Bereitschaft zur Leistung von Pikettdienst muss vorhanden sein

Umzugsunterstützung für berechtige Kandidaten wird bereitgestellt.

Lonzas Produkte und Services wirken sich täglich positiv auf Millionen von Menschen aus. Für uns stellt dies nicht nur eine grosse Ehre, sondern auch eine grosse Verantwortung, dar. Wie wir unsere Geschäftsergebnisse erreichen ist für uns genauso wichtig wie unsere Erfolge selbst. Bei Lonza wird Respekt grossgeschrieben und wir schützen sowohl unsere Mitarbeiter als auch unsere Umwelt. Erfolg für uns bedeutet moralisch vertretbarer Fortschritt.

Zu Lonza kommen Menschen, die Herausforderungen annehmen und mit ihrer Kreativität im Bereich Life Science neue Ideen für komplexe Problemstellungen entwickeln. Zusammen leisten wir einen Beitrag, der das Leben vieler Menschen auf der ganzen Welt verbessern kann. Dies bietet ihnen die Gewissheit und die Zufriedenheit, mit der eigenen Arbeit wirklich einen Unterschied zu machen.

weniger ansehen

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

We are looking for a visionary Head of EHS - Advanced Synthesis to join our Visp site and drive the strategic integration of Environment, Health & Safety across a dynamic, global business platform. In this key leadership role, you will shape a proactive safety culture, ensure regulatory compliance, and lead a team of EHS and process safety experts.

This is a unique opportunity for an experienced leader with a strong background in chemical or pharmaceutical manufacturing, who thrives in complex environments and wants to make a lasting impact on safety performance worldwide. If you're ready to combine EHS excellence with innovation and global collaboration-this role is for you.

Key Responsibilities

Act as the lead EHS contact for the Visp site and provide expert support to our site in Nansha (China).

Develop and implement EHS strategies to ensure regulatory compliance and operational excellence.

Lead a team of EHS professionals and drive cross-site alignment of safety programs and practices.

Represent EHS at senior leadership level and cultivate a strong safety culture throughout the organization.

Coordinate incident investigations, risk assessments, and continuous improvement initiatives.

Ensure effective communication and collaboration between site, platform, and corporate EHS functions.

Requirements

University degree or equivalent experience in Engineering, Chemistry, Occupational Safety, or a related technical field; advanced degree preferred.

Extensive EHS leadership experience in the chemical or pharmaceutical industry.

Deep knowledge of process safety, explosion protection, and industrial risk management.

Established proficiency in guiding teams, engaging partners, and inspiring change in a matrixed organization.

Strategic, analytical approach with strong communication skills.

Proficient in English; German is a strong asset.

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the happiness that comes with improving lives all around the world. The happiness that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

weniger ansehen

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

The site in Visp, Switzerland is growing and for our Biologics organization, we are seeking experienced Bioprocess Engineers with significant work experience in Downstream Processing (DSP) Manufacturing and a passion for Biotechnology to join our Lonza talent community. Become part of this great opportunity and apply now for the position as Principal Bioprocess Engineer DSP!

The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

Join our team at Bioatrium now!

What you'll do:

Plan and run operational activities in Downstream Processing, including tech transfer support, material planning, document and batch record preparation, training, and deviation handling.

Act as a functional lead for an interdisciplinary team of operators, supervisors, and specialists, ensuring smooth execution and high performance in assigned areas.

Guide and support daily operations for commercial manufacturing in defined DSP areas (e.g. purification, filling)

Ensure efficient operation of purification equipment for therapeutic protein production.

Maintain compliance with GMP and safety standards.

Key Responsibilities:

As Senior Bioprocess Engineer, you will plan and manage operational activities in Downstream manufacturing, e.g. tech transfer support, material planning, document and electronic batch record preparation, training and troubleshooting or deviation handling.

Act as a functional lead for an interdisciplinary team of production personnel, supervisors and specialists and be accountable for the performance and results of assigned projects.

Guide and support activities for commercial manufacturing in one or more defined DSP areas, e.g. capture, intermediate purification, polishing or drug substance filling.

Ensure efficient operation of single-use and/or stainless steel equipment for the purification of therapeutic proteins from mammalian expression systems.

Guide, support and train junior engineers.

Lead large scale cross-functional optimization projects.

Key Requirements:

Bachelor, Master's Degree or PhD in Biotechnology, Bio-chemical Engineering, Biochemistry or related Life Science subject.

Significant work experience (>5 Years) in Downstream Processing. Manufacturing in the biotech/biopharma industry e.g. chromatography, ultra-/diafiltration and final filling.

In-depth knowledge of downstream processing techniques.

Excellent GMP understanding.

Good knowledge of MES/DeltaV system is a plus.

Excellent communication skills in English and/or German.

Strong team orientation.

Structured, well-organized working attitude and solution-oriented working style.

Open-minded for new ideas and suggestions.

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

weniger ansehen

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

The site in Visp, Switzerland is growing and for our Biologics organization, we are seeking experienced Bioprocess Engineers with significant work experience in Downstream Processing (DSP) Manufacturing and a passion for Biotechnology to join our Lonza talent community. Become part of this great opportunity and apply now for the position as Principal Bioprocess Engineer DSP!

The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

Join our team at Bioatrium now!

What you'll do:

Plan and run operational activities in Downstream Processing, including tech transfer support, material planning, document and batch record preparation, training, and deviation handling.

Act as a functional lead for an interdisciplinary team of operators, supervisors, and specialists, ensuring smooth execution and high performance in assigned areas.

Guide and support daily operations for commercial manufacturing in defined DSP areas (e.g. purification, filling)

Ensure efficient operation of purification equipment for therapeutic protein production.

Maintain compliance with GMP and safety standards.

Key Responsibilities:

As Senior Bioprocess Engineer, you will plan and manage operational activities in Downstream manufacturing, e.g. tech transfer support, material planning, document and electronic batch record preparation, training and troubleshooting or deviation handling.

Act as a functional lead for an interdisciplinary team of production personnel, supervisors and specialists and be accountable for the performance and results of assigned projects.

Guide and support activities for commercial manufacturing in one or more defined DSP areas, e.g. capture, intermediate purification, polishing or drug substance filling.

Ensure efficient operation of single-use and/or stainless steel equipment for the purification of therapeutic proteins from mammalian expression systems.

Guide, support and train junior engineers.

Lead large scale cross-functional optimization projects.

Key Requirements:

Bachelor, Master's Degree or PhD in Biotechnology, Bio-chemical Engineering, Biochemistry or related Life Science subject.

Significant work experience (>5 Years) in Downstream Processing. Manufacturing in the biotech/biopharma industry e.g. chromatography, ultra-/diafiltration and final filling.

In-depth knowledge of downstream processing techniques.

Excellent GMP understanding.

Good knowledge of MES/DeltaV system is a plus.

Excellent communication skills in English and/or German.

Strong team orientation.

Structured, well-organized working attitude and solution-oriented working style.

Open-minded for new ideas and suggestions.

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

weniger ansehen

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

The site in Visp, Switzerland is growing and for our Biologics organization, we are seeking experienced Bioprocess Engineers with significant work experience in Downstream Processing (DSP) Manufacturing and a passion for Biotechnology to join our Lonza talent community. Become part of this great opportunity and apply now for the position as Principal Bioprocess Engineer DSP!

The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

Join our team at Bioatrium now!

What you'll do:

Plan and run operational activities in Downstream Processing, including tech transfer support, material planning, document and batch record preparation, training, and deviation handling.

Act as a functional lead for an interdisciplinary team of operators, supervisors, and specialists, ensuring smooth execution and high performance in assigned areas.

Guide and support daily operations for commercial manufacturing in defined DSP areas (e.g. purification, filling)

Ensure efficient operation of purification equipment for therapeutic protein production.

Maintain compliance with GMP and safety standards.

Key Responsibilities:

As Senior Bioprocess Engineer, you will plan and manage operational activities in Downstream manufacturing, e.g. tech transfer support, material planning, document and electronic batch record preparation, training and troubleshooting or deviation handling.

Act as a functional lead for an interdisciplinary team of production personnel, supervisors and specialists and be accountable for the performance and results of assigned projects.

Guide and support activities for commercial manufacturing in one or more defined DSP areas, e.g. capture, intermediate purification, polishing or drug substance filling.

Ensure efficient operation of single-use and/or stainless steel equipment for the purification of therapeutic proteins from mammalian expression systems.

Guide, support and train junior engineers.

Lead large scale cross-functional optimization projects.

Key Requirements:

Bachelor, Master's Degree or PhD in Biotechnology, Bio-chemical Engineering, Biochemistry or related Life Science subject.

Significant work experience (>5 Years) in Downstream Processing. Manufacturing in the biotech/biopharma industry e.g. chromatography, ultra-/diafiltration and final filling.

In-depth knowledge of downstream processing techniques.

Excellent GMP understanding.

Good knowledge of MES/DeltaV system is a plus.

Excellent communication skills in English and/or German.

Strong team orientation.

Structured, well-organized working attitude and solution-oriented working style.

Open-minded for new ideas and suggestions.

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

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