Göteborg: Quality Specialist

Are you Qing’s next colleague with Medical device and/or Life Science knowledge and experience?

Qing is a consultant company, with focus on Optimizing Quality and Regulatory compliance. We believe that quality is the foundation for delivering sustainable growth and enables great results in a predictable way.

 

Qing has extended competence and focus on the Medical device and Life Science area. Our vision is to be the first choice for organizations when they want to reach effectiveness and full compliance by using external resources to develop their business. As we are quality specialists within several areas, we can apply best practice and use knowledge from all industries by internal team work and competence sharing.

Our consultants thrive to help our customers. We support our clients from great ideas to a final product to benefit patients. At Qing we are experts to ensure that products are safe, efficient and fulfill all legal and regulatory requirements. We make the journey for CE-marking clear and market access efficient without jeopardizing patient safety.

 

We are growing and now want you to be part of our growth!

If you are a Medical Device quality and regulatory specialist with a passion to help others and want to be part of something big in a small and effective organization, apply for our open position as Quality Specialist.

Our customers are organizations of all sizes which mean that you will work with different types of customer projects. It could be shorter assignments as perform internal audits, risk analysis or filling a position at the customer site. Longer projects could be but are not limited to facilitating the work to implement or improve an existing Quality Management System (QMS), temporary filling a position or act as QA/RA resource in product development projects. We also support organizations in MDR or IVDR transitions.

 

Your personal abilities are most valuable for us and if you have knowledge and specialist competence in some or all the below parts, don’t hesitate to apply:

 

You are:

Organized and structured
Business minded
Communicative and networking
Showing high integrity
Team player with a positive attitude
 

You have experience in some or all of the following areas:

ISO 13485:2016/ 21 CFR 820
QMS configuration and process development
Product Development/Design Control/Project Quality
CAPA Management
Regulatory requirements and registration of products in EU and US
Risk Management (ISO 14971)
Internal and/or Supplier Audits
IEC 62304
IEC 82304
ISO 11607 (Packaging)
IVDR
 

Experience is meriting but not crucial.

 

Why Qing?

Qing sees every employee, has a team work approach, and is partly owned by our employees. This gives opportunities to impact the strategy of your employer, encourage exploration of your own interest and share the profit of our efforts. We invest in our employee's- as this is our greatest asset. 

Qing is a quality consulting company, part of Vinngroup, with Headquarter at Kvarnbergsgatan 2 in Gothenburg. You will meet and can network with an exciting mix of people as researchers, software developers, engineers, brand strategists, IT-specialist and entrepreneurs. 

 

Har du några frågor? 


Kontakta Bethina Frostad på recruitmore, bethina@recruitmore.se.