Laboratory Engineer - Quality Control

Do you want to work in an innovative and meaningful environment where quality and development are in focus? We are looking for a driven and meticulous laboratory engineer to join our team in Solna. 

About us

Valneva’s vision is a world in which no one dies or suffers from a disease that can be prevented by vaccination. Valneva has several vaccines in development, including the world’s first chikungunya vaccine, the only Lyme borreliosis vaccine candidate in partnership with Pfizer, and candidates against other global health threats.

Valneva’s portfolio also includes two commercial vaccines for travelers: one against Japanese encephalitis and one against cholera. Valneva operates internationally across Austria, Sweden, the UK, France, Canada and the USA.

Valneva Sweden AB has a long history in Sweden and today operates from Solna.

Learn more at www.valneva.com

About the role

This is a broad and varied Laboratory Engineer role combining routine Quality Control testing with investigations, troubleshooting, validation and qualification activities, and continuous improvement.

The Quality Control department is responsible for release testing of vaccines and their components, as well as raw materials and packaging materials. The scope also includes sampling and testing related to Environmental Monitoring (EM) and utilities, such as purified water, gases, and steam, to ensure compliance with GMP requirements and support the microbiological control of the manufacturing environment.

The position offers the opportunity to work across several areas of Quality Control within a GMP-regulated pharmaceutical environment and to contribute both to day-to-day laboratory activities and the continued development of our processes and ways of working.

Key responsibilities

• Perform and review routine Quality Control analyses according to established methods, including analytical techniques, immunoassays, and microbiological analyses.
• Ensure that laboratory activities are performed in accordance with GMP requirements, approved procedures, and internal instructions.
• Lead and document investigations related to deviations, OOS/OOT results, and other laboratory events.
• Lead and support method validation and verification activities, as well as qualification of laboratory instruments and equipment.
• Drive and contribute to troubleshooting, method optimisation, and laboratory improvement activities.
• Contribute to the development and implementation of efficient laboratory processes and best practices.
• Prepare, review, and update laboratory procedures, instructions, and other relevant documentation.
• Coordinate and order materials, reagents, and other supplies required for laboratory methods and activities.
• Collaborate cross-functionally with Quality Assurance, Manufacturing, Regulatory Affairs, and other relevant functions.
• Participate in internal and external inspections and audits, including preparing documentation and responding to questions related to the laboratory area.
• Provide analytical and technical support to the organisation and train colleagues in relevant methods, processes, and laboratory activities when required.

Qualifications & Experience

• University degree (BSc or MSc) in a relevant scientific field, such as Chemistry, Biotechnology, Life Sciences, or similar.
• Minimum 3 years of relevant laboratory and Quality Control experience within the pharmaceutical or biotechnology industry.
• Good knowledge of GMP and applicable regulatory requirements.
• Experience in leading or independently managing investigations, including deviations, OOS/OOT, CAPA, and Change Controls.
• Experience with validation and qualification activities within a laboratory environment.
• Ability to work independently, take ownership, and manage tasks in a structured and organised manner.
• Experience with laboratory computerised systems such as LIMS, Empower, or similar platforms is considered an advantage.
• Excellent verbal and written communication skills in both Swedish and English.

We place great value on personal qualities. You are meticulous, responsible, and quality-focused, with a collaborative mindset and the ability to work effectively both independently and as part of a team.

Employment & Benefits

This is a permanent, full-time position based at our Solna site, with a six-month probationary period.

We believe collaboration is strongest when we meet in person while still offering flexibility. The role follows Valneva Sweden's hybrid working model, with at least 50% of working time spent on-site in Solna.

As part of Valneva, you will receive a competitive employment package under the applicable Swedish collective agreement, including:

• ITP occupational pension
• Annual wellness allowance
• Access to occupational health services
• Vaccinations and reimbursement for medical visits and prescription medicines
• Eligibility for Valneva's annual bonus and stock option programmes

You will join an international organisation where your work contributes to our mission of developing, manufacturing and commercialising vaccines that address unmet medical needs.

How to apply

Application deadline: 27 September 2026

We review applications and conduct interviews on an ongoing basis, so we encourage you to apply as soon as possible.

Please submit your CV and, where applicable, cover letter in English through our careers site.

For GDPR reasons, we are unable to accept or review applications sent by email.

Our recruitment process includes reference checks, a comprehensive background check and drug test for the final candidate.

For questions about the position or recruitment process, please contact [email protected].

We respectfully decline contact from recruitment agencies, staffing companies and other suppliers regarding this recruitment.