Visp, Wallis, Switzerland · On-site
Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. The Contamination Prevention & Control (CPC) Environmental Moni…
Skills: Environmental Monitoring, GMP Compliance, Contamination Control, Microbiology, Audit Defense
Bend, Oregon, United States · On-site
The actual location of this job is in Bend, Oregon. Relocation assistance is available for eligible candidates and their families, if needed. In this role, you will play a key part in ensuring the reliability and complia…
Skills: Laboratory Instrumentation, Calibration, Troubleshooting, Validation Procedures, Computer System Validation
Stein, Aargau, Switzerland · On-site
The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Join Lonza AG as a (Senior) QA Expert Compliance, partnering with se…
Skills: Quality Management Systems, GMP Compliance, CAPA Management, Change Control, Deviation Investigation
Singapore, Singapore · On-site
Today, Lonza remains 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 dedicated people working tog…
Skills: cGMP Compliance, Aseptic Techniques, Clean Room Practices, Batch Record Execution, Environmental Monitoring
Colmar, Grand Est, France · On-site
$29k–$39k/yr
Lieu: Colmar Ce que ce poste vous apportera Une carrière agile et un environnement de travail dynamique. Un cadre professionnel inclusif et éthique. Des programmes de rémunération valorisant la performance. Une gamme d’a…
Skills: Microbiological Analysis, Environmental Monitoring, OOS/OOT/OOE Investigations, Laboratory Documentation, Quality Control
Singapore, Singapore · On-site
The Quality Assurance Department is looking for Specialist, QA to join the team. You will be supporting day-to-day Quality Assurance activities in accordance with approved SOPs / Policies for a multi-product, cGxP contra…
Skills: Quality Assurance, cGxP Compliance, GDP Corrections, Problem Solving, Data Analysis
Geleen, Limburg, Netherlands · On-site
$29k–$41k/yr
Production Logistic Associate Geleen, The Netherlands 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 sc…
Skills: GMP, Cleanroom Operations, Logistics, Production Support, Decontamination Equipment Operation
Manchester, England, United Kingdom · Hybrid
Global Head Finance Training & Learning Location: Manchester Hybrid Working Policy – 2 days in the office, 3 days WFH We are looking for a Director, Global Finance Training & Learning to define and drive the global strat…
Skills: Finance Training Strategy, Learning & Development, Finance Transformation, Stakeholder Management, Change Management
Visp, Wallis, Switzerland · On-site
Umzugsunterstützung steht berechtigen Kandidaten und ihren Familien bei Bedarf zur Verfügung. Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist. Wir sind …
Skills: Logistics Coordination, Inventory Management, 3PL Management, SAP EWM, SAP WM
Visp, Wallis, Switzerland · On-site
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…
Skills: Microbiological Analysis, GMP, Endotoxin Measurement, Germ Identification, Analytical Methods
Greenwood, South Carolina, United States · On-site
Diagnostics Technician (12hr Night Shift) Location: Greenwood, SC 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…
Skills: Hard Capsule Machine Operation, Quality Control, Troubleshooting, Sample Collection, Documentation
Greenwood, South Carolina, United States · On-site
Advanced Setup Technician I 12-hour Night Shift 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 scientif…
Skills: Equipment Setup, Troubleshooting, SCADA, SharePoint, Quality Checks
Portsmouth, New Hampshire, United States · On-site
Senior QA Specialist - Operations Location: This position is based in our Portsmouth, NH office. The standard schedule is a 10-hour first shift, Wednesday through Saturday, with working hours from 7:00 AM to 5:30 PM EST.…
Skills: Batch Record Review, Lot Release, cGMP Compliance, Technical Writing, Quality Management Systems
Vacaville, California, United States · On-site
$160k–$266k/yr
Technical Project Manager Location: Vacaville, California, USA Lead complex, high-impact capital investment projects supporting biologics manufacturing at Lonza’s Vacaville site. In this role, you will drive projects fro…
Skills: Technical Project Management, Project Engineering, Capital Investment Management, Biologics Manufacturing, Commissioning And Qualification
Singapore, Singapore · On-site
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,…
Skills: cGMP Compliance, Aseptic Techniques, Clean Room Practices, Environmental Monitoring, Batch Record Documentation
Tampa, Florida, United States · On-site
Pharmaceutical Warehouse Operator Shift: 1st shift Location: Tampa, FL Join Lonza as a Pharmaceutical Warehouse Operator and play a vital role in ensuring safe, accurate, and compliant material handling within our state‑…
Skills: Forklift Operation, Material Handling, Inventory Management, Good Documentation Practices, ERP Systems
Visp, Wallis, Switzerland · On-site
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,…
Skills: Deviation Management, CAPA, cGMP Compliance, People Management, Project Management
Geleen, Limburg, Netherlands · Hybrid
$50k–$70k/yr
Production Team Lead Geleen, Netherlands Lead a high-performing manufacturing team and play a key role in delivering life-changing cell and gene therapies to patients around the world. This is an exciting opportunity to …
Skills: People Leadership, Operational Excellence, GMP Compliance, Team Development, Continuous Improvement
Portsmouth, New Hampshire, United States · On-site
MSAT Sr. Scientist, Analytical Development Services Location: 100% on-site. Portsmouth, NH. The MSAT Senior Scientist, Analytical Development Services (ADS) incumbent is responsible for performing Analytical Development …
Skills: Analytical Development, Assay Work, Instrument Troubleshooting, Data Analysis, cGMP
Tampa, Florida, United States · On-site
Job Title Engineer, Packaging Location Tampa, Florida, USA Join our Tampa site as a Packaging Engineer, where you will play a critical role in supporting GMP packaging processes and delivering high-quality pharmaceutical…
Skills: GMP Packaging Processes, Process Validation, Equipment Qualification, Technical Writing, SOP Development
Visp, Wallis, Switzerland • On-site
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
The role involves authoring GMP-compliant environmental monitoring reports and leading complex contamination investigations to maintain a state of control. The specialist will act as a Subject Matter Expert during audits and implement continuous improvement initiatives within reporting workflows.
Requires a university degree in Biology, Biotechnology, Microbiology, Chemistry, or Engineering with a strong background in GMP and contamination control. Proficiency in data science tools like R, Python, or Power BI is considered an advantage.
Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.
The Contamination Prevention & Control (CPC) Environmental Monitoring (EM) team delivers critical GMP compliance outputs across the whole Visp site, including EM Batch Reports (part of the batch release process), PQ monitoring reports, periodic trend evaluations, microbiological house-flora reports and monitoring data assessments required to demonstrate and maintain a state of control. As a QA Specialist, you will strengthen data-driven quality oversight within environmental and utility monitoring, combining hands-on GMP expertise with a structured, data-informed approach to contamination oversight. You will take ownership of compliance-ready EM outputs and complex investigations, acting as SME in audits and inspections.
You will contribute to how monitoring data is collected, analysed, visualised and used to support risk-based decisions and proactive contamination prevention.
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. Our full list of tailored local benefits can be found below.
Benefits in Visp: https://bit.ly/3wjkoFi
Author GMP-compliant EM reports for EM and CU monitoring, integrating microbiological expertise, and site knowledge from investigations and facility walkdowns in support of CCS maintenance and decision-making.
Support the review of EM outputs for batch release and certification, coordinating with relevant stakeholders to ensure timely delivery in line with batch release requirements
Combine knowledge from cleanroom and production walkdowns with data collected from various GMP Quality systems to identify trends and assess contamination control status.
Present and defend monitoring performance, deviations, and related actions as SME in audits and inspections.
Ensure compliance with SOPs, GMP, and internal quality requirements.
Lead and support complex investigations across facilities and departments, using EM data and trends and contamination control knowledge to reach well-founded conclusions
Contribute to cross-departmental CCS status dashboards and other reporting and visualization tools.
Identify and implement continuous improvement opportunities within reporting workflows, including lean and 6S initiatives, to reduce manual effort, eliminate waste and increase process standardisation
University degree (PhD/Master/Bachelor) in Biology/ Biotechnology/ Microbiology/ Chemistry/ Engineering or related field.
Strong scientific and technical background ideally with microbiology and contamination control knowledge, including familiarity with environmental and utility monitoring programs.
Solid knowledge of GMP and regulatory requirements, including experience writing audit-ready GMP documentation (SOPs, work instructions, trend reports).
Experience presenting and defending GMP documentation and reports to auditors and inspectors in a regulated environment
Experience with data science tools such as R and/or Python and/or experience with Power BI or Power Automate is an advantage.
Experience with MODA, TrackWise, LIMS, or comparable GMP systems is preferred.
Ability to work autonomously, take ownership of deliverables, and drive tasks forward independently while managing competing priorities across routine and strategic workstreams.
Strong cross-functional collaboration and communication skills in English and preferrably in German.
Structured, proactive, and solution-oriented working style.
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.
Making the Medicines of Tomorrow
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow. Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs. For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.
Offices: Muenchensteinerstr. 38, Basel, 4002, CH · 8830 Biggs Ford Road, Walkersville, MD 21793, US · 35 Tuas South Ave 6, SG, 637377, SG · 228 Bath Road, Slough, Berkshire SL1 4DX, GB · Rottenstrasse 6, Visp, VS 3930 , CH
Making the Medicines of Tomorrow
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow. Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs. For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.
Offices: Muenchensteinerstr. 38, Basel, 4002, CH · 8830 Biggs Ford Road, Walkersville, MD 21793, US · 35 Tuas South Ave 6, SG, 637377, SG · 228 Bath Road, Slough, Berkshire SL1 4DX, GB · Rottenstrasse 6, Visp, VS 3930 , CH
