Jobs bei GXP CONSULTING Switzerland Sàrl

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GXP CONSULTING Switzerland Sàrl - Lausanne, Waadt, 1003(Seit 2 Tagen)
Qualification / Validation Engineer M/F Job Description: 1.Skills/Knowledge Required · Master’s degree in scientific or engineering discipline. · More than 2 years’ experience in equipment qualification IQ, OQ, PQ. · More than 2 years’ experience in the Pharmaceutical/Biotech sectors. · Competent with current FDA and EU regulatory regulations and best practices. · Experiences with GAMP. · Fluent (...
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GXP CONSULTING Switzerland Sàrl - Bâle, Basel Stadt, 4000(Seit 2 Tagen)
Regulatory Affairs Specialist PROJECT DESCRIBTION: Life cycle management RA support, for sterilization site change from external to internal OVERALL RESPONSIBILITIES Support the internal Regulatory Affairs group in creation and maintenance of technical documentation supporting compliance to · European Council Directive 92/42/EEC or Regulation 2017/745, as applicable, · As well as country registrat...
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GXP CONSULTING Switzerland Sàrl - Lausanne, Waadt, 1003(Seit 2 Tagen)
Senior Software and Embedded Engineer Purpose and scope of the job As member of the Software team, the Senior Software Development Engineer will be responsible for: · The design, development, maintenance and verification. · The authoring and maintenance of technical documentation required for CE marking and FDA approval. · The continuous improvement of software quality, reliability and safety. Mai...
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GXP CONSULTING Switzerland Sàrl - Lausanne, Waadt, 1003(Seit 3 Tagen)
Manufacturing Engineer OVERALL RESPONSIBILITIES : This role is for a Junior Project Lead for Documentation activity related to the transfer of production from one external supplier to existing internal capacity. The activity is to be performed in a productive site for Medical Devices (plates, needles and instruments) mostly involving drilling and turning CNC machines. Experience with such machiner...
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GXP CONSULTING Switzerland Sàrl - Lausanne, Waadt, 1003(Seit 3 Tagen)
Human Factors Engineer You’ll be in charge of leading human factors activities within medical device development projects. You will be responsible for independently leading, planning, executing and reporting human factors activities to be performed during the development of medical device/combination product as required by the current relevant regulations. It includes managing user studies and inf...
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