Quality Assurance professionals for future assignments

Job description
Are you an experienced Quality Assurance Specialist with a passion for quality and safety in the pharmaceutical or medtech industries? Do you have expertise with regulatory requirements and want to be part of a company that strives to make a difference in people's health? Submit your spontaneous application to us.
We at Randstad Life Science are continuously looking for qualified QA professionals for future assignments. As a consultant with us, you become part of a dynamic network where your knowledge and experience can be used in various projects within quality management. Therefore, we encourage candidates with a relevant background and expertise in QA, from the pharmaceutical or medtech industry, to reach out even if we currently don’t have a listed position.
Why submit a spontaneous application to us?
At Randstad Life Science, we are always interested in getting to know competent and driven individuals interested in working as consultants within the pharmaceutical and medtech industry. Even if we are not currently advertising a specific QA role, we highly value proactive applications and look forward to exploring future collaboration opportunities with the right candidates.
If this has piqued your interest - we welcome your application! Please make sure your CV and personal letter are in the same document. We will reach out to you if a position that fits your qualifications becomes available.

Responsibilities
Since this is a spontaneous application to cover future assignments in Quality Assurance, the scope of your initial assignment and your work tasks may vary depending on the assignment and client.
As a Quality Assurance professional, you may work with:
Implementing and maintaining the Quality Management System (QMS) in line with GMP, ISO 13485, and FDA regulations.
Conducting internal and external audits, and ensuring that the processes meet the highest standards of product safety and quality.
Developing and following up on quality deviations, risk assessments, and handling CAPA processes.
Collaborating with various departments to ensure quality control at all stages of production.
Preparing and supporting regulatory inspections and reporting.


Qualifications
We are looking for someone who:
Has a relevant higher education in fields such as chemistry, biotechnology, pharmaceuticals, medical technology, or similar.
Has 3+ years of experience in quality assurance within the pharmaceutical or medtech industry.
Possesses deep knowledge of GMP, ISO 13485, and other relevant standards and regulations.
Documented knowledge of GCP is an advantage
Has experience in audits and regulatory inspections is highly advantageous.
Is detail-oriented, organized, and has excellent collaboration skills.
Is fluent in English, in speech and writing.
Good communication skills in Swedish is an advantage.


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.