Quality Assurance Specialist Wanted

We are looking for an experienced Quality Assurance specialist who will play a key role this spring in ensuring that our client's processes, routines, and systems are functioning optimally. You will be an important part of the work to follow up on quality, drive improvements, and ensure that the business complies with applicable regulations.

We are seeking a Quality Assurance specialist who, in the short term until summer, will support the organization in work related to processes, routines, and systems, including case management. The role means that you will be a vital part of ensuring quality and following up that the business operates according to established routines and regulations.

We offer an intensive introduction, but you need to bring experience in quality work - preferably ISO 9001 (ISO 13485 is a plus but not a requirement). Experience from Medtech is a bonus, but not necessary.

Responsibilities

• Ensure that quality management and quality assurance are followed according to routines.
• Follow up on verification and validation activities.
• Report quality KPIs.
• Participate in and lead improvement work and goal setting.
• Ensure that the business complies with laws, regulations, and set goals.

Tasks

• Lead the work of establishing and maintaining quality in purchasing and production flows.
• Support verification and validation work within purchasing, production, and production technology.
• Support documentation and risk management.
• Participate in supplier audits.
• Coordinate CAPA activities, quality deviations, and complaints.
• Prepare and analyze measurement data as a basis for decision-making.
• Conduct product audits and follow up on changes.

We are looking for someone who has

• Experience in quality work, preferably ISO 9001.
• Good understanding of processes and routines.
• Ability to work independently and drive improvement work.
• Desirable: experience from Medtech and ISO 13485.

Start: Immediately
Scope: Consulting assignment until summer, with the possibility of takeover.
Working hours: Daytime, weekdays, full-time - Some possibility for remote work exists.

Your Employment

The position means that you will be employed by Jefferson Wells but will spend your working days at our client's location in Tranemo. This is a consulting assignment lasting 6 months, with the goal of transitioning to the client.

About Jefferson Wells

As a consultant at Jefferson Wells, you receive employment with all that it entails in terms of competitive salary, overtime compensation, vacation, occupational pension, and insurance according to collective agreements. Of course, you have a consultant manager available to you throughout your employment period, responsible for your assignments, ensuring you enjoy your workplace, and helping you develop in your professional role.

If you have any questions, please contact Therese Johansson via email: [email protected] (mailto:[email protected])

We look forward to hearing from you!