Pharmaceutical Technologist

☞ CK QLS

見る: 195

更新日: 24-04-2024

場所: Fribourg Fribourg FR

カテゴリー: 健康/医療

業界: Medical Equipment Biotechnology Research Pharmaceutical Manufacturing

レベル: Associate

ジョブタイプ: Full-time

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仕事内容

  • Salary: Competitive
  • REF Number: 00052253
  • Consultant: Adrien Guimard
  • Contact: 0041 (0) 800 106 106
  • Date Published: 29.11.2021
  • Sector: Pharmaceutical
  • Location: Fribourg, Central Switzerland
  • Discipline: Technical - IT Project Manager, Technical - Maintenance Engineer
QLS are recruiting for a Pharmaceutical Technologist to join an important project with an innovative Pharmaceutical Company at their site based in Fribourg on a contract basis for one year with option of an extension.

Main Responsibilities
  • Set-up of quality target product profiles
  • Define and justify product specifications
  • Plan manufacturing process development studies in the context of assigned projects
  • Supervise the trials in the pharmaceutical lab where appropriate
  • Evaluation and documentation of manufacturing process study results
  • Coordination of the pharmaceutical and related analytical activities
  • Quality by design (QbD) approach is used in development projects and product support projects where appropriate
  • Establishment and definition of the design space if applicable
  • Compilation of risk analysis for validation activities, raw materials, and processes
  • Compilation of validation plans and reports, if applicable within the project
  • Collaboration with other departments and other sites as needed to assure good progress of the projects
  • Support for the compilation of manufacturing documents for manufacturing processes and for stability plans in context of the attributed projects
  • Supportfor the compilation of technical documentation for the submission of new products or variations to the authorities
  • Regular information to the superior on project progress and issues
  • Maintains his work in inspection readiness level and providesthe necessary support in any internal or external audit in addition to providing input to and review regulatory documentation
  • Resource and budget planning for transfers / product support projects
  • Proactively identify and propose process and technology improvements
Candidate’s Requirements
  • M.Sc. in pharmaceutical sciences or scientist with PhD in pharmaceutical technology with min. . 5 - 10 years of practical experience
  • Experience in collateral people management and project management
  • Experience in product transfers / product support projects
  • Fluent in French, both in oral and written
  • Professional level in English, both in oral and written communications
  • Good level of German, both in oral and written, is a plus
For more information or to apply for this position, please contact Adrien on 0041 (0) 800 106 106 or email aguimard@ckqls.ch. Please could you send any correspondence in English. Please quote reference QLS 00052253 in all correspondence.
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締切: 08-06-2024

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