Vacant job

ALTEN is now looking for a Process Engineer!

We are looking for you who are passionate about process development and technical problem-solving within biological manufacturing. Do you want to work with formulation, aseptic filling, and packaging of advanced biopharmaceuticals? Then this could be your next challenge as a consultant at ALTEN!

What 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 safe and sustainable future.
• Supportive and coaching leadership.
• The opportunity to work within the life science industry and other regulated environments.
• A personal education budget for internal or external courses.

What the role entails

As a Process Engineer at ALTEN, you will be part of a team that supports and develops formulation, filling, and packaging processes for biological medicines. You will work with technical support, deviation management, and continuous improvements in a GMP-regulated environment. The role involves close collaboration with manufacturing, automation, quality, and engineering to ensure stable and efficient processes.

• Support and improve formulation and aseptic filling of biological medicines.
• Investigate and solve process-related problems using structured troubleshooting and root cause analysis.
• Execute and evaluate improvement projects to increase quality, yield, and cost-effectiveness.
• Collaborate cross-functionally with various departments to ensure smooth product introductions and operations.
• Contribute to documentation such as work instructions, risk assessments, and technical reports.
• Support or lead validation activities (IQ/OQ/PQ) for new equipment and processes.

We are looking for you who:

We are looking for someone who is technically skilled, structured, and driven by delivering results. You thrive working both independently and in a team and have the ability to communicate clearly with various stakeholders.

• Experience with formulation and/or aseptic filling of biological medicines or similar processes.
• Knowledge of cGMP in regulated manufacturing.
• Knowledge of production equipment, facilities, and instrumentation.
• Experience from start-up environments, new facilities, or production lines.
• Knowledge of validation and qualification (IQ/OQ/PQ).
• Experience with GMP for sterile processes and aseptic regulatory requirements.
• Experience with Lean Manufacturing and documented improvements.
• Fluent in Swedish and English.

Duration: 9-month assignment, starting in August 2026.

Why ALTEN?

At ALTEN, you become part of a highly qualified team working on some of the most exciting projects within life science and technology. We offer a culture where you can grow, challenge yourself, and make a real difference in projects that shape future solutions.

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 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.

We look forward to receiving your application!