fortil

1 001 – 5 000 Darbuotojai

fortil yra Europos inžinerijos ir technologijų konsultacijų grupė, kurią įkūrė ir jai vadovauja inžinieriai verslininkai. Įmonė teikia pramonės ir verslo klientams inžinerijos, projektavimo bei techninių konsultacijų paslaugas aviacijos ir kosmoso, statybos ir BIM, telekomunikacijų, sveikatos priežiūros bei logistikos srityse. Daugiau nei 2 500 darbuotojų turinti daugiadalykė komanda veikia daugiau nei dešimtyje šalių, įmonėms teikdama specializuotą inžinerinę kompetenciją ir pagalbą įdarbinant darbuotojus. Darbuotojams priklausanti kapitalo struktūra atspindi dėmesį inžinerija grindžiamam bendradarbiavimui ir ilgalaikiam techninių sprendimų įgyvendinimui.

Darbai įmonėje

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.

prieš 2 savaites

Šveicarija Hibridinis Visas etatas Vidutinis lygis Vyresnysis specialistas Privaloma Kalba: anglų Privaloma Kalba: prancūzų Analitikas

Aprašymas

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.

Reikalavimai

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.

Privalumai

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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Jungtinės Valstijos Nuotolinis Visas etatas Vyresnysis specialistas Privaloma Kalba: anglų Pardavimai

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Nuotolinis Visas etatas Vidutinis lygis Vyresnysis specialistas Privaloma Kalba: anglų Pardavimai

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Atidaryti

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.

Aprašymas

Reikalavimai

Privalumai

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