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Bioprocess Engineer USP/DSP (Microbial)/BioConjugates (m/w/d) 80%-100%

Тип работы
fulltime
Английский
b2
Страна
Switzerland
Релокация
Switzerland
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
Bioprocess Engineer USP/DSP (Microbial)/BioConjugates (m/w/d) 80%-100% (Upstream/Downstream Processing and Bio-Conjugates): Supporting clinical and commercial biopharmaceutical manufacturing in Visp with an accent on cGMP execution, facility qualification, and specialized processing areas. Focus on troubleshooting equipment, evaluating batch results, managing deviations and CAPAs, developing automation recipes, and training production personnel.

Location: Visp, Switzerland. Relocation assistance is available for eligible candidates and their families.

Company

Global life sciences manufacturing organization supporting the development and production of medicines across more than 30 sites on five continents.

What you will do

  • Execute operational activities for clinical and commercial manufacturing while maintaining safety and quality standards.
  • Act as a subject matter expert in designing, commissioning, and qualifying new facilities and in preparing, cleaning, and changing over assigned areas.
  • Lead specialized areas including upstream processing, downstream processing, or Bio-Conjugates.
  • Perform cGMP manufacturing activities, including batch execution, test-result evaluation, equipment troubleshooting, and resolution recommendations.
  • Review production documentation, manage deviations and change requests, and implement CAPAs.
  • Develop and review automation recipes, train production personnel, and participate in audits and customer visits.

Requirements

  • Master’s degree or equivalent experience in Biotechnology, Biochemical Engineering, Biochemistry, Process Engineering, or a related Life Science field; alternatively, a bachelor’s degree with relevant pharmaceutical production experience.
  • Expertise in upstream processing, downstream processing, or bio-conjugation technology.
  • Experience in biomanufacturing and/or scaling up a biopharmaceutical facility; cGMP experience is advantageous.
  • Excellent English communication skills required.
  • Organized, goal-oriented, motivated, open to new ideas, and able to solve problems effectively.

Nice to have

  • German proficiency.

Culture & Benefits

  • Agile career development and a dynamic work culture.
  • Inclusive and ethical workplace focused on collaboration, accountability, excellence, passion, and integrity.
  • Performance-based compensation programs.
  • Lifestyle, family, and leisure benefits tailored to the Visp location.
  • Relocation assistance for eligible candidates and their families.

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