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fortil
fortil
1001 – 5000 Darbinieki
BūvniecībaLoģistikaVeselības aprūpe
fortil ir Eiropas inženierijas un tehnoloģiju konsultāciju grupa, ko dibinājuši un vada inženieri uzņēmēji. Uzņēmums atbalsta rūpniecības un korporatīvos klientus, sniedzot inženierijas, projektēšanas un tehnisko konsultāciju pakalpojumus tādās jomās kā aviācija un kosmosa nozare, būvniecība un BIM, telekomunikācijas, veselības aprūpe un loģistika. Daudznozaru komandā ir vairāk nekā 2500 darbinieku, un tā darbojas vairāk nekā desmit valstīs, nodrošinot uzņēmumiem specializētas inženierzināšanas un atbalstu darbinieku piesaistē. Darbiniekiem piederošā kapitāla struktūra atspoguļo uzņēmuma uzmanību uz inženierijas vadītu sadarbību un ilgtermiņa tehnisko risinājumu īstenošanu.
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Vakances uzņēmumā

QC Analyst – Biochemistry and Method Validation

Join fortil as a QC Analyst supporting biochemical testing and analytical method validation for regulated pharmaceutical projects. You will work with quality and analytical development teams in a collaborative environment.

CHŠveiceHibrīdiPilna slodzeVidējais līmenisVecākais speciālistsNepieciešamā Valoda: angļuNepieciešamā Valoda: frančuAnalītiķis

Apraksts

  • Conduct laboratory analyses and quality-control testing.
  • Apply analytical techniques including ELISA, Immunoblot / Western Blot, and qRT-PCR / qPCR.
  • Help implement and qualify new analytical methods on coagulation equipment.
  • Assist with preparing and executing analytical method protocols.
  • Analyze, verify, and review laboratory results.
  • Support investigations into atypical results, deviations, and nonconformities.
  • Maintain data traceability and compliant documentation in line with GMP requirements.
  • Work with QC, Quality Assurance, Analytical Development, and other project teams.
  • Contribute to analytical method transfer and lifecycle activities.

Prasības

  • Degree or equivalent training as a laboratory technician, biomedical analysis technician, biologist, biochemist, biotechnologist, or in a related field.
  • Some laboratory experience, preferably in pharmaceutical or biotechnology quality control or another strongly regulated setting.
  • Practical experience performing ELISA assays.
  • Experience using Immunoblot / Western Blot techniques.
  • Experience with qRT-PCR / qPCR methods.
  • Strong laboratory technique and documentation skills.
  • Familiarity with GMP / GxP requirements.
  • Ability to follow analytical protocols and interpret test results.
  • Detail-oriented, self-directed, and well organized.
  • Effective collaborator in multidisciplinary teams.
  • Fluent in French.
  • Professional working proficiency in English.
  • Experience with analytical method validation or transfer, coagulation assays, release or stability testing, analytical investigations, deviations and CAPA, or pharmaceutical QC is an advantage.

Priekšrocības

  • Individual guidance to support your professional growth.
  • Work on innovative, high-value industrial projects.
  • Entrepreneurial culture with room to take initiative.
  • Opportunity to become a shareholder in the group.
  • Strong focus on innovation, corporate social responsibility, and employee development.
  • Policies designed to support parenthood and work-life balance.
  • Positions are open to applicants with disabilities, irrespective of gender, background, or sexual orientation.

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