fortil
fortil
fortil este un grup european de consultanță în inginerie și tehnologie, fondat și condus de ingineri-antreprenori. Compania sprijină clienți industriali și corporativi prin servicii de inginerie, proiectare și consultanță tehnică în domenii precum industria aerospațială, construcțiile și BIM, telecomunicațiile, serviciile medicale și logistica. Echipa sa multidisciplinară, formată din peste 2.500 de angajați, activează în mai mult de douăsprezece țări, oferind companiilor expertiză specializată în inginerie și sprijin pentru recrutare. Structura capitalului deținut de angajați reflectă orientarea fortil către colaborarea bazată pe inginerie și furnizarea de soluții tehnice pe termen lung.

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.

Descriere

  • 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.

Cerințe

  • 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.

Beneficii

  • 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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