Sterilization and Cleanroom Expert

The Askersund Plant, with its 90-strong team, is a vibrant and innovative hub of quality excellence.

This exciting role offers an opportunity to work in a dynamic environment characterized by high ambitions to be at the forefront in all aspects of quality management. At Essity, you will be challenged to grow, and you have great opportunities to work with a fantastic team, contributing to the company's innovative and progressive work.

Our corporate culture emphasizes cooperation and personal development, fostering a strong entrepreneurial spirit within a familiar atmosphere. As a member of an inspiring and affirmative team, you will help others and work together towards set goals.

In this role, you will ensure that products and processes meet established specifications and quality standards while utilizing collected findings to identify opportunities for continuous improvement. You will collaborate closely with production, logistics, and project departments to guarantee product quality and process requirements are met.

You will act as a Role Model for Safety and Quality, training others and updating instructions and SOPs within the QMS. Furthermore, you will participate in the investigation of non-conformities and engage in cross-functional projects, requiring integrity and a non-prestigious approach when solving problems and collaborating.

1. Conduct inspections and establish quality standards for both in-process and finished products and materials.
2. Train and oversee the quality team and operators in their use of control forms, procedures, and correcting quality issues.
3. Act as Quality change manager.
4. Release final and semi-final products.
5. Ensure performance of yearly dose audits in cooperation with suppliers.
6. Provide QA knowledge and strategy as an internal representative for complex projects.
7. Apply quality principles, analyze quality records, prepare reports, and recommend improvements.
8. Conduct inspections, including verification and validation of components, materials, products, and clean rooms.
9. Identify and address recurring problems related to product quality or testing procedure reliability, documenting quality issues and performance measures for management review.
10. Lead Continuous Improvement projects, conducting root cause analysis activities, acting as CAPA owner, and performing process/product/software validations.
11. Perform internal audits.
12. Support customers/stakeholders with quality documentation upon request.

To succeed in this role, you should possess:

1. Proven experience working with sterilizing and clean rooms.
2. At least 2-3 years of experience working within Med-tech, pharmaceutical, or food production.
3. Excellent skills in English/Swedish, written and spoken.
4. Knowledge and experience working with ISO 13485 is preferred.

At Essity, we offer a range of benefits, including flexible working hours, wellness contributions, and access to favorable holiday accommodations through the Employee Foundation. Our collaborative and caring work environment empowers employees to reach their full potential.