Vacant job

We are now looking for a meticulous and driven Process Engineer within aseptic processing to join a growing Operations team in Uppsala. In this role, you will play a central part in ensuring the highest quality in aseptic manufacturing – contributing to safe, efficient, and compliant processes that truly make a difference.

About the Role

As a Process Engineer, you will become part of a cross-functional and collaborative production environment where quality, regulatory compliance, and continuous improvement are at the core. You will act as a quality support function within aseptic manufacturing, ensuring that processes, equipment, and documentation meet GMP requirements.

This role offers a unique opportunity to combine operational work close to production with the coordination of validation and quality activities, making you a key player in both daily operations and long-term development. The role also includes training in aseptic techniques, participation in external and internal inspections, and providing assessments in deviation investigations, among other tasks.

Key Responsibilities

• Act as a subject matter expert/technical expert in aseptic manufacturing processes, ensuring all work is performed in accordance with GMP and internal quality standards, with a strong focus on product safety and regulatory compliance.
• Plan, coordinate, and execute validation and (re)qualification activities for equipment and processes, ensuring they meet regulatory requirements and are fit for purpose.
• Contribute to the development and improvement of SOPs, instructions, and documentation, ensuring working methods are clear, up-to-date, and aligned with current standards.
• Support daily production through planning, handling deviations, CAPA, change control processes, and operator training, and participate in audits and inspections as a technical expert.

This is a permanent position with a major Life Science company in Uppsala.

About You

We are looking for someone who is results-oriented, curious, and brings positive energy. You combine personal drive with strong collaboration skills and thrive in a team environment. Above all, you are passionate about making a difference for consumers, patients, and healthcare professionals. We strive to strengthen every employee's development while meeting the business's needs, both now and in the future. We value diversity and respect the integrity and rights of every individual.

Key Requirements & Qualifications

• At least 5 years of experience in aseptic work within the pharmaceutical or medical technology industry, with practical experience in a GMP-regulated environment.
• A Bachelor's degree in Engineering, Life Sciences, or equivalent, providing a solid foundation for working in a regulated environment.
• Good understanding of quality processes such as deviations, CAPA, and change control, and experience working with documentation and regulatory requirements.
• Fluent in both Swedish and English, both verbally and in writing, with the ability to communicate effectively in both local and global contexts.

Application

Does this sound interesting? Don't hesitate to apply. We handle applications on a rolling basis, so don't wait to submit yours.