Our client is a leading portfolio medical technology company. They are now looking for a Quality Assurance Specialist.
Supporting all QA activities for a commercial organization.
Ensuring compliance with ISO 13485:2016 & GDPMD requirements.
Working with a cross-functional team to ensure compliance and bring improvements in the complete processes within the Sales, Marketing, and Distribution channel.
Conducting internal audits.
Supporting external audits by certifying agencies.
Conducting product and process quality checks following established work instructions and sampling plans, and ensure that all products and processes meet the standards, Customer, Quality, and regulatory requirements.
Bachelor's Degree in Biotech/Engineering/Pharma.
Has 3-4 years experience in implementing QMS as per ISO 13485-2016 / ISO 9001:2008/GDPMD requirements.
More than just a recruitment company. At PRTR, we have been a part of our customers’ success for 27 years as their total HR solutions partner. With 450 dedicated professionals and over 11,000 outsourced staff, we are here to be Your Partner In People because
PRTR believes in the power of people.