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- Senior Validation Engineer for Life Science Projects in Uppsala
Senior Validation Engineer for Life Science Projects in Uppsala
Alten Sverige AktiebolagStockholms län, Stockholm
Previous experience is desired
23 days left
to apply for the job
ALTEN is looking for a Senior Validation Engineer for exciting Life Science projects in Uppsala!
Are you an experienced validation engineer who thrives in an international environment where technology, quality, and collaboration are at the forefront? Do you want to work with advanced process equipment and play a key role in the validation work for some of the most innovative projects in Life Science? Then this could be the next step in your career. We are now looking for a Validation Engineer or Validation Lead for an exciting assignment with a leading Life Science company in Uppsala. Here you will have the opportunity to work with complex equipment, international collaborations, and qualification and validation activities throughout the entire project lifecycle.
What do we offer?
As a consultant at ALTEN, you will have the opportunity to work on challenging and exciting projects with some of our most important clients, including:
- Technical challenges and development opportunities.
- An inspiring community and the opportunity to contribute to a sustainable and automated future.
- Supportive and coaching leadership.
- The possibility to work within different industries where our clients operate.
- A personal education budget for internal or external courses.
The Role
In the role of Validation Engineer / Validation Lead, you will be an important part of a team responsible for validation activities related to process equipment and production systems. The work covers everything from installation and qualification of equipment to testing and documentation according to current regulatory requirements. You will primarily work with Vendor Package Equipment (VPE) – complete deliveries from suppliers that include mechanical components, electrical and control systems, and associated documentation.
Your main responsibilities include:
- Planning, executing, and documenting validation activities within CQV.
- Writing and reviewing IQ/OQ/PQ protocols and associated reports.
- Participating in FAT and SAT activities as well as verification and testing of equipment.
- Collaborating with suppliers, project teams, and global stakeholders.
- Traveling to the USA to conduct tests and ensure that equipment meets requirements and specifications.
- Reviewing colleagues' documentation and providing technical support within the validation field.
- Ensuring that all work is performed in accordance with GDP and regulatory guidelines.
- Sharing knowledge and supporting colleagues in the team's continued development.
The role involves close collaboration with teams in different parts of the world, which requires good communication skills and flexibility. Occasional meetings outside regular working hours may occur to facilitate collaboration between Sweden and the USA.
Requirements
We are looking for you who have experience with:
- CQV/validation including IQ, OQ, and PQ.
- Work with PLC and automation systems.
- Process technology equipment such as skids, autoclaves, or CIP/SIP systems.
- Creation and review of validation protocols and reports.
- Good Documentation Practice (GDP).
- Swedish and English in speech and writing.
- Work in GMP-regulated operations within Life Science or the pharmaceutical industry.
- Travel is a natural part of the role, and it is a requirement that you have the opportunity to travel internationally, approximately four times per year.
- You thrive in an international environment and are flexible when occasional meetings need to be adjusted to different time zones.
Preferred Qualifications
It is an extra plus if you also have experience with:
- FAT, SAT, and other testing activities related to equipment deliveries.
- Veeva.
- Leading or coordinating roles within validation.
Timeframe: Consulting assignment starting in August 2026.
Why apply?
This is an opportunity to become part of an exciting project where you have significant influence over deliveries, quality, and results. You will work together with engaged colleagues in a social team that values collaboration, knowledge sharing, and a positive work environment.
For those who enjoy technology, travel, international contacts, and the opportunity to make an impact, this is a role with both variety and development potential.
About ALTEN
ALTEN is one of Europe's largest technology and IT consulting firms with over 60,000 employees in more than 30 countries. In Sweden, we are approximately 1,300 consultants across 11 locations, from Malmö to Skellefteå, supporting world-leading companies within Automotive, Telecom, Industry, Energy, Aerospace & Defense, and Life Science.
For the sixth year in a row, ALTEN has been named one of Sweden's most attractive employers by Karriärföretagen.
Welcome to read more about us at alten.se (https://alten.se).
We look forward to your application!
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