Quality Technicians

Job description
We at Randstad Life Sciences are currently looking for two quality technicians for full-time consultant positions of one year assignment. The two positions will cover different stages of the quality control process: one position is for a technician responsible of the final release of the product (dental implants and corresponding tools) and the second one is for a technician responsible of collecting, reviewing and archiving related products documentation.


Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.

Responsibilities
As a Quality Technician you will perform final inspection and final release of products and make sure that all activities have been performed according to instructions.


 The Quality Technician final release will perform several different activities within the group including:
·       Inspection of sterile and non-sterile product documentation.
·       Be part of continuous improvement projects.
·       Archiving of batch documentation.


The Quality Technician final inspection will perform varying activities including:
·       Archiving of batch documentation.
·       Be part of continuous improvement projects.
·       Perform Incoming Inspection of components.


For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.
Deadline 31st of August - the selection process and interviews will be ongoing. The starting date will be as soon as possible and agreed by all parties.
For more information: Please contact Meriem Echbarthi, meriem.echbarthi@randstad.se.
Please note that applications sent through email will not be processed and deleted due to GDPR.

Qualifications
We think you are a positive and driven team player. You are open for challenges and enjoy working together with highly skilled and committed colleagues where every day makes a difference. We believe you have:


 Minimum requirements:
·       High School/College/Higher vocational education (yrkeshögskola) or equivalent background.
·       Analytic and structured approach.
·       Good and meticulous at following instructions.
·       A careful, responsible way of working.
·       Good writing skills as we have high demands on documentation.
·       Good communication and interpersonal skills as parts of the work is done in cross functional teams.
·       Good knowledge of standard Microsoft Office applications.
·       Language skills in Swedish. English skills are beneficial.
 
Preferred requirements:
·       Experience from regulated business.
·       It is also considered an advantage if you are familiar with ISO 13485:2016 Medical Device – Quality Management System and FDA Quality System Regulation 21 CFR Part 820 or have experience from medical device or other product areas with high regulatory demands.
·       Experience from manage measurement instruments, such as calipers, micrometers etc.

About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential. With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward.