Switzerland, Stein
The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.
Be part of an exciting growth project where you’ll contribute to set up a new QC lab! Routine analysis of a large variety of release and stability tests will be the majority of the work. However, besides the routine analysis you will also execute method validation and transfer activities of various physico-chemical methods in order to facilitate implementation. Check out Your Career in Drug Product Services at Lonza !
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 Will 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 global benefits can be found at https://www.lonza.com/careers/benefits
What You Will Do
Ensuring the release of life saving medicines by executing, coordinating and reviewing physico-chemical and biochemical Drug Product release and stability testing under cGMP according to existing method SOPs (e.g. compendial testing/content/identity/purity for biologics/large molecules) – methods used: ELISA, HPLC, iCIEF, UV-VIS, CE-SDS and many others.
Responsible to document assay execution under cGMP following Good Documentation Practices (GDP) and flag relevant observations to the supervisor for further assessment
Accountable for execution of operational tasks in the lab, e.g. mobile phase preparations, calibration of equipment, adherence to and maintenance of 6S, consumable management and support of equipment maintenance.
Support of validation and transfer activities in frame of new project introductions.
Contribution to investigation/troubleshooting for assigned tasks
Support in authoring of cGMP documents e.g. procedures (SOPs) or quality records (e.g. OOE/OOS records, CAPA`s)
What We Are Looking For
Solid work experience in Quality Control in the GMP controlled environment
Solid hands‑on experience with either ELISA or HPLC or iCIEF is a must (experience with multiple methods is preferred)
Experience in analytical method validation and method transfer is a plus
Apprenticeship as Lab technician, Bachelor, Master or equivalent in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related field
Knowledge of lab quality systems like LIMS, Tiamo or CDS like Empower/Chromeleon
Fluency in written and spoken English is a must, German is an asset
Ability to work independently and in a dynamic & fast‑pacing project environment. Proactive attitude
Reference: R77599
#J-18808-Ljbffr
The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.
Be part of an exciting growth project where you’ll contribute to set up a new QC lab! Routine analysis of a large variety of release and stability tests will be the majority of the work. However, besides the routine analysis you will also execute method validation and transfer activities of various physico-chemical methods in order to facilitate implementation. Check out Your Career in Drug Product Services at Lonza !
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 Will 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 global benefits can be found at https://www.lonza.com/careers/benefits
What You Will Do
Ensuring the release of life saving medicines by executing, coordinating and reviewing physico-chemical and biochemical Drug Product release and stability testing under cGMP according to existing method SOPs (e.g. compendial testing/content/identity/purity for biologics/large molecules) – methods used: ELISA, HPLC, iCIEF, UV-VIS, CE-SDS and many others.
Responsible to document assay execution under cGMP following Good Documentation Practices (GDP) and flag relevant observations to the supervisor for further assessment
Accountable for execution of operational tasks in the lab, e.g. mobile phase preparations, calibration of equipment, adherence to and maintenance of 6S, consumable management and support of equipment maintenance.
Support of validation and transfer activities in frame of new project introductions.
Contribution to investigation/troubleshooting for assigned tasks
Support in authoring of cGMP documents e.g. procedures (SOPs) or quality records (e.g. OOE/OOS records, CAPA`s)
What We Are Looking For
Solid work experience in Quality Control in the GMP controlled environment
Solid hands‑on experience with either ELISA or HPLC or iCIEF is a must (experience with multiple methods is preferred)
Experience in analytical method validation and method transfer is a plus
Apprenticeship as Lab technician, Bachelor, Master or equivalent in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related field
Knowledge of lab quality systems like LIMS, Tiamo or CDS like Empower/Chromeleon
Fluency in written and spoken English is a must, German is an asset
Ability to work independently and in a dynamic & fast‑pacing project environment. Proactive attitude
Reference: R77599
#J-18808-Ljbffr
(Senior) Scientist QC 80-100% Arbeitgeber: Lonza
Als Arbeitgeber in Visp, Schweiz, bieten wir Ihnen die Möglichkeit, in einem dynamischen Umfeld zu arbeiten, das Innovation und Teamarbeit fördert. Unsere Unternehmenskultur legt großen Wert auf persönliche Entwicklung und Weiterbildung, sodass Sie Ihre Fähigkeiten als Data Engineer kontinuierlich erweitern können. Darüber hinaus profitieren Sie von attraktiven Zusatzleistungen und der Unterstützung bei einem möglichen Umzug, um sicherzustellen, dass Sie sich schnell in Ihrer neuen Umgebung wohlfühlen.
