Jobs › Companies › Valneva › Senior Engineer, Supply Chain (SCM)

À propos de ce poste Senior Engineer, Supply Chain (SCM) chez Valneva

Valneva · Sur site · Solna, Stockholm County, Sweden

Do you enjoy taking ownership of compliance, improving processes and working closely with others to maintain high quality standards? Valneva Sweden is looking for an experienced Senior Engineer, Supply Chain (SCM) 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.

Our work focuses on developing, manufacturing and commercialising vaccines that address unmet medical needs. Valneva Sweden AB has a long history in Sweden and today operates from Solna.

Learn more at www.valneva.com

About the role

As Senior Engineer, Supply Chain (SCM), you will lead and develop GxP compliance within Supply Chain Management in Sweden, combining ownership of quality processes with hands-on work in documentation, validation and continuous improvement.

Your scope covers inbound deliveries, the storage and handling of starting materials, consumables, work in progress and finished products, and distribution to internal and external customers. You will help ensure that SCM processes meet applicable GxP requirements and that compliance activities are planned and completed in line with business needs.

Working closely with colleagues across functions, customers and service providers, you will turn regulatory requirements into clear, practical ways of working. You will report to the Head of Supply Chain Management and regularly communicate progress, priorities and compliance risks.

Key responsibilities

  • Lead and develop GxP compliance for SCM Sweden, monitor regulatory developments and implement improvements to processes and ways of working.
  • Own SCM GxP documentation, coordinating and performing updates, developing new documents and reviewing logbooks to keep records current, clear and easy to follow.
  • Own, coordinate and carry out SCM activities in the quality management system (QMS), and act as a key user for documentation, deviations, corrective and preventive actions (CAPA) and change control systems.
  • Act as the SCM lead for internal and external audits, taking ownership of corrective and preventive actions and ensuring they are implemented where needed.
  • Lead and execute validation and qualification activities, own the validation master plan and ensure planned activities are carried out.
  • Own the SCM Sweden maintenance plan and ensure that activities are completed on time. Follow up with cleaning service providers to ensure cleaning is effective and meets required standards.
  • Lead GxP onboarding for new employees and complete required training within agreed timelines.
  • Identify and initiate projects that simplify processes, improve efficiency and strengthen GxP compliance across SCM Sweden.
  • Plan and schedule GxP activities in line with business priorities, identify dependencies across departments and coordinate with internal and external customers and service providers.
  • Document and report progress regularly to the Head of Supply Chain Management and escalate GxP compliance risks to the appropriate level.

Requirements

Requirements and experience

  • Experience working in a GxP-regulated environment, with a strong understanding of applicable regulations and how to translate them into practical processes.
  • Strong GxP skills and the ability to take ownership of compliance activities, documentation and quality-related tasks.
  • Proficiency in Microsoft tools, including Project, Excel, Word and PowerPoint, and good general IT skills.
  • Strong written and verbal communication skills, with the ability to influence, motivate and collaborate across functions and organisational levels.
  • The ability to plan, prioritise and manage competing workloads, meet deadlines and make sound decisions independently.

It is an advantage if you have

  • Experience working in GxP-regulated manufacturing.

Who we are looking for

You are structured, organised and detail-oriented, with a strong sense of ownership. You work independently, follow through on commitments and take a proactive approach to identifying improvements and anticipating risks.

You combine a strong quality and compliance mindset with pragmatic, risk-based judgement. You turn requirements into workable solutions and remain focused when priorities compete.

You communicate clearly and collaborate well with others, building effective relationships across departments and with external partners. You are confident challenging existing ways of working and escalating concerns when needed to protect quality and compliance.

Benefits

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 therefore 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 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 bonus and stock option programmes


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

How to apply

Application deadline: 2026-11-09

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

Please note that our recruitment process includes a comprehensive background check and drug test for the final candidate.

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

For GDPR reasons, we do not accept or review CVs or applications sent by email. All applications must be submitted through our careers site.

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

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À propos de Valneva

We are a specialty vaccine company that develops, manufactures, and commercializes prophylactic vaccines for infectious diseases addressing unmet medical needs. We take a highly specialized and targeted approach, applying our deep expertise across multiple vaccine modalities, focused on providing either first-, best- or only-in-class vaccine solutions.

We have a strong track record, having advanced multiple vaccines from early R&D to approvals, and currently market three proprietary travel vaccines, including the world’s first and only chikungunya vaccine, as well as certain third-party vaccines.

Revenues from our growing commercial business help fuel the continued advancement of our vaccine pipeline. This includes the only Lyme disease vaccine candidate in advanced clinical development, which is partnered with Pfizer, as well as vaccine candidates against the Zika virus and other global public health threats.

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