Vacant job

At Avaron, you get the security of a permanent position combined with the variety of working on-site with different clients. We recruit specialists in everything from technology, IT, and industry to project management and business support – and regardless of the assignment, you have a consultant manager who is there for you and your development.

You will step into a high-tech and quality-critical production environment where stable processes are crucial for both delivery and patient safety. As a Process Engineer, you will work close to daily operations with a focus on strengthening existing processes, solving problems near production, and driving long-term improvements simultaneously.

You will become a key process technology expert in commercial production and product launch on existing lines. The focus is on fill-finish, where you collaborate closely with production, quality, and technical functions to create robust, sustainable solutions that work in practice.

This is a role for you who want to combine hands-on problem-solving with improvement work and validation in a regulated environment where your work makes a real difference.

• You monitor process performance, such as yield, quality, as well as stops and disruptions, and drive actions that strengthen robust operations.
• You lead or contribute to deviation investigations, root cause analyses, risk assessments, and CAPA related to process and equipment.
• You plan, coordinate, and execute activities within qualification and validation, including review and approval of protocols and reports such as IQ/OQ/PQ.
• You support the launch of new products on existing production lines and ensure that process-related activities are carried out in a structured manner.
• You participate as a process technology expert during audits and regulatory inspections and contribute to ensuring that working methods and documentation meet cGMP requirements.
• You contribute to digitalization, standardization, and development of working methods and tools that simplify daily life in production.

• University degree in technology or natural sciences, for example in chemistry, biology, biotechnology, process engineering, or mechanical engineering.
• Experience working in a regulated industry.
• Understanding of the interplay between product requirements, materials, process, and equipment.
• Good understanding of cGMP and quality requirements in production.
• Experience in driving or leading qualification and validation activities.
• Ability to work structured with documentation.
• Good knowledge of Swedish and English, both spoken and written.

• Experience from pharmaceutical manufacturing.
• Experience with aseptic filling and/or sterile manufacturing.

• Permanent employment at Avaron AB
• Pension plan
• Wellness allowance of 5,000 SEK per year

We are hiring continuously – please apply as soon as possible.