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Start: 1.6. or by arrangement

Tasks

  1. Analytical project management of customer projects
  2. Support in obtaining and maintaining the integrated management system

Requirements

  • Natural science degree, FH, Master or Ph.D. (preferably chemistry, pharmacy, biochemistry)
  • Professional experience in a pharmaceutical environment
  • Proven GxP knowledge and experience in ISO 17025
  • Good technical knowledge in instrumental and wet chemical analysis and data evaluation (especially chromatography, titrations, spectroscopic analysis, elemental analysis)

All Details about the Tasks and Requirements can be found on our career page.

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This year Suisse Technology Partners AG was once again able to prove its high competence as a service company as well as its adaptability to new standards. From now on, ISO 17025 services are available to customers according to the currently valid version "2018".

Whereas the standards of ISO 17025:2005 were previously valid, ISO 17025:2018 is now applied. In addition to numerous innovations, the new version of the ISO standard places increased emphasis on confidentiality and impartiality. Here Suisse Technology Partners AG was able to prove itself as a competent and trustworthy partner.

Customer requirements will continue to be met at the highest level as Suisse Technology Partners AG enters the new year with the highest level of quality.

The new certificates are now available in English and German under Downloads.

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Companies operating in the medtech sector can now access a new complete service offering, which provides support for product development from planning to market launch. Not least the EU regulation 2017/745 on medical devices (medical device regulation) poses great challenges for many companies. Suisse Technology Partners AG and QUO AG from Opfikon jointly offer a comprehensive range of services, which can be accessed on the website https://medtech-solutions.ch

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We are looking to strengthen our "inorganic analytics" team as of July 1, 2020 or by appointment:

Tasks:

  • Independent planning, execution, evaluation, assessment and documentation of elemental analyses (ICP-MS, ICP-OES, AAS, XRF), among others in GMP and ISO 17025 environment
  • Development and validation of methods as well as statistical data evaluation and documentation according to GMP and ISO regulations in close cooperation with the customer
  • Creation of quality-relevant documents (e.g. analysis regulations, SOPs, WIs) and processing of deviations, OOSs and CoCs
  • Active participation in the continuous improvement of systems, laboratory organisation and documents
  • Participation in internal and external audits within the framework of ISO 9001, ISO 17025 and GMP
  • Close cooperation with the organic analysis and R&D departments of Suisse Technology Partners AG within the scope of development projects
  • Substitute of the laboratory responsible for "Elemental analysis

more details on our career page

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The Praxiszirkel Verpackungsentwicklung „von der Simulation bis zum Test“, which took place on 22 May 2019 at Suisse Technology Partners AG in Neuhausen, brought together experts along the value chain. They discussed open questions, showed successful practical examples and thus created the basis for joint projects or an improved development process. The Packaging Development Practice Circle is organized by inno-pack.net. It is aimed at experts from industry or universities who deal with issues in the field of packaging development, simulation and testing. If you are interested in the exchange, please contact Dieter Franzke from inno-pack.net directly.

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