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Siegfried DINAMIQS Ltd. is a Contract Development and Manufacturing Organization (CDMO) based in Schlieren's Bio-Technopark right next to Zurich (Switzerland) specializing in the manufacturing of viral vectors for gene therapy applications.
At DINAMIQS, we offer a comprehensive range of services, including process development, research-grade vector manufacturing, and analytical testing. With state-of-the-art R&D and GMP facilities, we are dedicated to supporting gene therapy projects with scalable and efficient solutions.
DINAMIQS has been acquired by Siegfried in 2023 and is now looking to grow its dedicated team of experts by hiring a QC Specialist GMP.
In this role, you will play a key part in driving the success of DINAMIQS by leveraging your skills within a newly established, fast-growing GMP QC analytics team.
Your role
As part of the GMP quality control team, you will perform a wide range of laboratory testing activities, including:
* Molecular biology assays for viral vector products, such as qPCR, ELISA, and Western blotting.
* Perform microbiological testing for WFI, environmental monitoring and media fill tests.
* Maintain eucaryotic cell lines and perform cell-based in vitro tests, such as infectivity assays.
In addition you will:
* Perform, evaluate and document analytical testing activities for drug product, in-process control and stability samples under GMP following company policies and SOPs.
* Participate in validation activities for new analytical methods.
* Contribute to laboratory sample logistics, by registering materials to the LIMS system and ensuring accurate and complete documentation.
* Regularly check stock levels and shelf-life of critical laboratory consumables.
* Assume responsibility for selected laboratory instruments regarding regular performance checks and maintenance schedule.
* Take responsibility for general laboratory tasks, such as cleaning of labware, autoclaving and buffer preparation.
Your profile
* Apprenticeship as laboratory technical assistant (chemistry, biology) or B.Sc or M.Sc. in relevant field (such as biochemistry or molecular biology)
* At least 2+ years of experience working with biopharmaceutical products, ideally viral vectors
* At least 1-2 years of work experience in a GMP quality control environment
* Proficiency with various molecular biology techniques used in viral vector quantification and analysis of impurities, such as PCR-based methods, ELISA, SDS-PAGE
* Experience with microbiological testing methods (water testing, bioburden, environmental monitoring)
* Experience with cell culture techniques (thawing, maintaining, cell-banking)
* Working experience with LIMS systems
* Fluent in written and spoken English, with the ability to communicate and work seamlessly in an international QC team
What you can expect
* A unique work experience, being part of one of the most dynamic, diverse and inclusive CDMOs in the industry.
* 5 weeks holidays and flexible working hours make it possible to combine family, leisure time and career.
* Impactful Work: Make a significant difference through innovative gene therapy projects.
* Learning Opportunities: Develop diverse skills in a dynamic environment.
Are you interested in joining a motivated team with a start-up culture? Then take the next step and send us your application via LinkedIn.
Seniority level
* Seniority level
Entry level
Employment type
* Employment type
Full-time
Job function
* Job function
Science and Manufacturing
* Industries
Pharmaceutical Manufacturing
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