Visp, Wallis, Switzerland · On-site
Relocation assistance is available for eligible candidates and their families, if needed. Join our Bioprocess DSP Team in Visp as Bioprocess Engineer for MMM MC1 DSP 80-100% (m/f/d) and be part of a world‑class environme…
Skills: Bioprocess engineering, Downstream processing, Chromatography, Virus inactivation, Depth filtration
Basel, Basel-City, Switzerland · On-site
The actual location of this job is in Basel Tower, Switzerland. We are looking for a Legal Counsel to support our Licensing Business. The role will focus on partnering with a dynamic and growing business in the evaluatio…
Skills: Contract drafting, Contract negotiation, Legal advisory, Commercial law, Licensing agreements
Portsmouth, New Hampshire, United States · On-site
QA Compliance Specialist - LSA Location: This position is based in our Portsmouth, NH office. The typical work schedule is Monday through Friday, 7:00 AM–4:00 PM EST. What you will get: Below you will find a comprehensiv…
Skills: Quality Assurance, Compliance, GMP, Quality Systems, CAPA
Visp, Wallis, Switzerland · On-site
Der Arbeitsort dieser Stelle befindet sich in Visp, Schweiz. Anspruchsberechtigten Bewerbern und ihren Familien steht bei Bedarf Unterstützung beim Umzug zur Verfügung. Der Produktionsbetrieb Accelerate in Visp ist gesta…
Skills: Production process monitoring, GMP compliance, Technical understanding, Manual dexterity, IT literacy
Geleen, Limburg, Netherlands · On-site
$41k–$58k/yr
QA Specialist / Officer II Geleen, Netherlands The actual location of this job is in Geleen, Netherlands. Join our Quality Assurance team and play a key role in ensuring that life-changing medicines are manufactured to t…
Skills: Quality Assurance, GMP, Batch record review, Compliance, Deviation management
Hyderabad, Telangana, India · Hybrid
Regulatory Affairs Specialist Location: Hyderabad, India (Hybrid) ***Relocation assistance is available for eligible candidates and their families, if needed. Join Lonza’s Global Capability Center (GCC) in Hyderabad and …
Skills: Regulatory affairs, CMC documentation, Clinical trial applications, Product lifecycle management, Veeva Vault
Basel, Basel-City, Switzerland · On-site
The actual location of this job is in Basel Tower, Switzerland. As Global Category Manager Laboratory Supplies, you will play a key role in shaping global sourcing strategies that support research, development and manufa…
Skills: Category management, Strategic sourcing, Procurement, Supplier management, Contracting
Portsmouth, New Hampshire, United States · On-site
Job Title: Manufacturing Associate III Location: Portsmouth, NH, (On-site) As a Manufacturing Associate III at our Portsmouth site, you will play a key role in upstream production of therapeutic proteins that support pat…
Skills: Upstream bioprocessing, cGMP, Manufacturing equipment operation, CIP, SIP
Portsmouth, New Hampshire, United States · On-site
Quality Control Manager - PM Location: Portsmouth, NH. The Quality Control (QC) Manager, PM leads QC operations and manages cross-functional projects in a manufacturing setting to ensure strict regulatory compliance. The…
Skills: Quality control, Project management, Regulatory compliance, cGMP, Laboratory performance
Houston, Texas, United States · On-site
Deviation Investigation Writer - Viral Vector Location: This is an on-site position located in Houston, TX. Available shift: Monday through Friday, standard office hours (approximately 8:00 a.m. to 5:00 p.m.) The Deviati…
Skills: Deviation investigation, Root cause analysis, CAPA development, Technical writing, cGMP compliance
Visp, Wallis, Switzerland · On-site
Der Arbeitsort dieser Stelle befindet sich in Visp, Schweiz. Anspruchsberechtigten Bewerbern und ihren Familien steht bei Bedarf Unterstützung beim Umzug zur Verfügung. Der Produktionsbetrieb Accelerate in Visp ist gesta…
Skills: Team leadership, Production management, cGMP compliance, Technical maintenance, Quality control
Hyderabad, Telangana, India · Hybrid
Regulatory Affairs Senior Specialist Location: Hyderabad, India (Hybrid) ***Relocation assistance is available for eligible candidates and their families, if needed. Join Lonza’s Global Capability Center (GCC) in Hyderab…
Skills: Regulatory affairs, CMC documentation, Dossier authoring, Drug substance filing, Product lifecycle management
Hyderabad, Telangana, India · Hybrid
Regulatory Affairs Senior Specialist Location: Hyderabad, India (Hybrid) ***Relocation assistance is available for eligible candidates and their families, if needed Join Lonza’s Global Capability Center (GCC) in Hyderaba…
Skills: Regulatory affairs, CMC documentation, Dossier authoring, Veeva Vault, eCTD publishing
Singapore, Singapore · On-site
The Career Conversion Program (CCP) training period lasts for 15 months. Structured on-the-job training (OJT) will be provided and conducted at the participating companies to facilitate the application of learning and to…
Skills: Biotechnology, Pharmaceutical sciences, Biomedical engineering, Good manufacturing practices, Standard operating procedures
Visp, Wallis, Switzerland · On-site
Ort: Visp (Schweiz) Bei Bedarf steht für berechtigte Kandidaten und ihre Familien Unterstützung beim Umzug zur Verfügung. Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kont…
Skills: Sterility testing, Microbiology, GMP, Quality control, Method development
Visp, Wallis, Switzerland · Hybrid
The actual location of this job is in Visp, Switzerland. We are looking for a CSV Smart Technology Trainee to join our Computerized System Validation (CSV) team on a 2 years fixed term contract. In this role you will con…
Skills: Computerized System Validation, Data science, Python, AI/ML, Data analytics
Bangkok, Thailand · On-site
This is a fully site‑based role at Bangkok. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. We a…
Skills: Accounting, Finance, Tax, General ledger, Month-end close
Portsmouth, New Hampshire, United States · On-site
Job Title: Quality Control Analyst I – Microbial Control Location: Portsmouth, NH, (On-site) As a QC Analyst II, Chromatography, you will play an important role in supporting the release of in-process and final product d…
Skills: Chromatography, HPLC, GMP, Analytical testing, Protein A
Singapore, Singapore · On-site
The Attached and Train raining period lasts for 15 months. Structured on-the-job training (OJT) will be provided and conducted at the participating companies to facilitate the application of learning and to ensure that i…
Skills: GMP Manufacturing, Aseptic Technique, Equipment Monitoring, Laboratory Tasks, CIP/SIP Operations
Visp, Wallis, Switzerland · On-site
The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Join our growing Ibex™ Solutions team in Visp and play a key leadership r…
Skills: Downstream processing, Biologics manufacturing, GMP compliance, Team leadership, Process engineering
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You will be responsible for executing and optimizing downstream purification steps such as chromatography, filtration, and filling to ensure product quality and compliance. Additionally, you will act as the functional lead for manufacturing execution, cleaning, and changeover activities within the assigned area.
Candidates must hold a Master's degree in Biotechnology, Biochemical Engineering, or a related field, or a Bachelor's degree with relevant pharma production experience. A few years of biomanufacturing experience and a strong understanding of GMP and bioprocess technology are required.
Relocation assistance is available for eligible candidates and their families, if needed.
Join our Bioprocess DSP Team in Visp as Bioprocess Engineer for MMM MC1 DSP 80-100% (m/f/d) and be part of a world‑class environment where innovation meets purpose. You’ll play a key role in purifying life‑saving therapies while collaborating with talented experts in a dynamic, high-performance setting. If you’re passionate about biotechnology and want to make a real impact, this is your opportunity.
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.
An agile career and dynamic working 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 in Visp can be found on https://bit.ly/3wjkoFi
Ensure that operational activities for clinical and/or commercial manufacturing are performed on-time and within given safety and quality standards
Act as the functional lead for preparation, manufacturing execution, cleaning and changeover in the assigned area
You will be responsible for executing and optimizing downstream purification steps—such as chromatography, virus inactivation, depth filtration, TFF, and filling—to ensure product quality, yield, and compliance with GMP standards.
In charge of one or more defined DSP areas (e.g. gain, polishing or filling) for the purification of therapeutic proteins from mammalian (Bioprocess Engineer DSP)
Master’s Degree or equivalent experience in Biotechnology, Biochemical Engineering, Biochemistry or related Life Science subject, or Bachelor’s holder with experience in pharma production
Knowledge in either USP (such as bioreactors) or DSP units (such as chromatography)
Couple of years working experience in biomanufacturing required
GMP experience and understanding of bioprocess technology
Excellent communication skills in English, good German skills of advantage
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
