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QC / IPC Lab Technician 100%, (m/w/d)

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Employment type
Full-time
Location
Liestal
First posted
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  • 14 septembre 2026
  • 100%
  • Indefinite duration
  • Eichenweg 1 A, 4410 Liestal
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CordenPharma is one of the leading contract development and manufacturing organizations (CDMO) and develops and produces active pharmaceutical ingredients, medicines and associated packaging services on behalf of its clients as a "full-service" provider. The group employs approximately 3,000 employees.

Our network in Europe and the United States offers flexible and specialized solutions for five technological platforms: peptides, lipids & carbohydrates, injectables, highly potent active ingredients & oncology as well as small molecules. We aim for excellence in supporting this network and we are committed to providing products of the highest quality for the benefit of patients.

CordenPharma International (CPI) acts as the management company of the CordenPharma group. In addition to the executive management team, CPI houses central functions such as sales & marketing, legal, human resources and business development, which operate on an international and inter-site scale for the CordenPharma group.

We are looking for immediate entry or by agreement for a

QC / IPC Technician 100 %, (m/f/d) Chemistry specialty - in the field of quality control & in-process control #

  • Liestal
  • as soon as possible or by agreement
  • full time
  • permanent position

Your tasks ##

  • Performing in-process controls (IPC) in accordance with current testing procedures and test methods
  • Support during the release analysis of raw materials, intermediate and finished products in accordance with current testing procedures and test methods
  • Analysis, documentation and evaluation of analytical results in compliance with GMP requirements
  • Performing purity tests on equipment

Your profile ##

  • Completed training as a chemistry technician or equivalent training
  • At least 2 years of professional experience in an analytical laboratory, ideally in a regulated GMP pharmaceutical environment
  • Experience with HPLC, GC, DC, spectroscopic methods and titrations
  • Ideally experience with Chromeleon software
  • Good knowledge of GMP guidelines
  • Very good knowledge of German
  • Autonomous, structured and solution-oriented way of working
  • Availability for flexible hours (supporting production)

What we offer you ##

An attractive and performance-based salary package ####

An attractive position with a high degree of responsibility ####

Contribution to public transport costs ####

Short commutes and direct communication with all departments ####

Does this suit you? ##

If you like working in a team and are interested in a varied area of responsibility, if it is natural for you to think and act beyond your own field, then you are in the right place with us!

Do you have any questions?

Do you still have questions regarding your application, the position or other? I will be happy to answer them.

Jacqueline Steiner
Senior HR Generalist
E-mail : bewerbung.cpi@cordenpharma.com

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Posted 3 days ago

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