GMP QC Lab Engineer - Hybrid Solna

Valneva

Solna kommun

Hybrid

SEK 550,000 - 700,000

Full time

14 days+

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Benefits offered by this job

ITP occupational pension

Annual wellness allowance

Occupational health services

Vaccinations and medical reimbursement

Annual bonus and stock options

Job summary

Valneva Sweden AB is seeking a meticulous Laboratory Engineer to join the Solna team. The role combines routine QC testing with investigations, validation, and continuous improvement in a GMP-regulated environment.

You will work across QC areas, support deviations and OOS/OOT investigations, and contribute to process optimisation. A BSc/MSc in a relevant field, plus 3 years in pharma/biotech QC, is required, with fluency in Swedish and English.

Qualifications

Bachelor’s or Master’s degree in Chemistry, Biotechnology, Life Sciences or related field.
Minimum 3 years of laboratory/Quality Control experience in pharma/biotech.
Strong GMP knowledge and regulatory understanding.
Experience leading investigations (deviations, OOS/OOT, CAPA).
Experience with validation/qualification activities.
Fluent Swedish and English.

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.