Senior Sales Director, Digital Advertising
ViamediaLead digital advertising sales for Viamedia, building agency and brand partnerships and closing omnichannel deals. The role carries an annual quota of $1.5 million to $2.5 million.
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fortil is a European engineering and technology consulting group founded and led by engineer-entrepreneurs. The company supports industrial and corporate clients with engineering, design, and technical consulting services across fields including aerospace, construction and BIM, telecommunications, healthcare, and logistics. Its multidisciplinary team of more than 2,500 employees works across over a dozen countries, providing specialist engineering expertise and recruitment support for businesses. fortil’s employee-owned capital structure reflects its focus on engineering-led collaboration and long-term technical delivery.
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.
Description
- 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.
Requirements
- 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.
Benefits
- 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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