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Senior Quality Assurance Specialist
3 days ago
The Askersund Plant, with approximately 90 employees, boasts a modern organization structure.
This stimulating environment is 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.
About the RoleIn 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.
- Conduct inspections and establish quality standards for both in-process and finished products and materials.
- Train and oversee the quality team and operators in their use of control forms, procedures, and correcting quality issues.
- Act as Quality change manager.
- Release final and semi-final products.
- Ensure performance of yearly dose audits in cooperation with suppliers.
- Provide QA knowledge and strategy as an internal representative for complex projects.
- Apply quality principles, analyze quality records, prepare reports, and recommend improvements.
- Conduct inspections, including verification and validation of components, materials, products, and clean rooms.
- Identify and address recurring problems related to product quality or testing procedure reliability, documenting quality issues and performance measures for management review.
- Lead Continuous Improvement projects, conducting root cause analysis activities, acting as CAPA owner, and performing process/product/software validations.
- Perform internal audits.
- Support customers/stakeholders with quality documentation upon request.
We seek someone who is structured, meticulous, and enjoys documentation. Additionally, you must have:
- Proven experience working with sterilizing and clean rooms.
- At least 2-3 years of experience working within Med-tech, pharmaceutical, or food production.
- Excellent skills in English/Swedish, written and spoken.
- Knowledge and experience working with ISO 13485 is preferred.
At Essity, we encourage all employees to challenge themselves to grow and reach their full potential. This position offers an exciting and varied work environment where you can influence and develop your work. You will work in a well-organized and collaborative team, benefiting from flexible working hours, wellness contributions, and access to favorable holiday accommodations through the Employee Foundation.
We look forward to welcoming you to our team.
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