Vacant job

Job Description

Are you a meticulous quality assurer with a passion for microbiology and GMP? At Randstad Life Sciences, we are seeing an increased demand from our clients in the pharmaceutical industry in the Stockholm/Södertälje region.

We are proactively looking for someone who wants to take the next step in their career as a consultant with us. We have several exciting openings in Quality Assurance (QA) starting this spring, where you will have the chance to work in international environments with life-saving products.

The Role in Brief

As a QA Specialist, you will work with quality assurance in a highly regulated environment. The tasks vary depending on the specific assignment but often include:

• Reviewing and approving documentation.
• Ensuring compliance with GMP and other regulatory requirements.
• Cross-functional collaboration with production, QC, and warehouse/logistics.
• Handling deviations and change requests.

Who Are You?

To be considered for these roles, you need to meet the following basic requirements:

• Academic degree: At least 240 ECTS (or 160 credits) in natural sciences, including at least 7.5 ECTS in microbiology.
• Experience: At least 1 year of experience in QA/QC within the pharmaceutical industry.
• Knowledge: Good understanding of GMP and pharmaceutical manufacturing.
• Language: Very good ability to communicate in both Swedish and English.

It is a significant plus if you have:

• Experience in sterile manufacturing or biological products.
• Previous experience in material quality or supplier management.
• A strong microbiological background.

Your Career at Randstad Life Sciences

As a consultant with us at Randstad Life Sciences, you get the best of both worlds: the security of a stable employment with collective agreements and benefits, combined with the opportunity to gain broad experience with industry-leading pharmaceutical companies.

We are experts in Life Science and understand your everyday life. We are here as your career partner to support you, challenge you, and ensure that you land an assignment where your skills truly make a difference.

Application

We are working with ongoing selection to quickly match the right person when assignments start in April and May. Therefore, do not wait to submit your CV!

Responsibilities

• Reviewing and approving documentation.
• Ensuring compliance with GMP and other regulatory requirements.
• Cross-functional collaboration with production, QC, and warehouse/logistics.
• Handling deviations and change requests.

Qualifications

• Academic degree: At least 240 ECTS (or 160 credits) in natural sciences, including at least 7.5 ECTS in microbiology.
• Experience: At least 1 year of experience in QA/QC within the pharmaceutical industry.
• Knowledge: Good understanding of GMP and pharmaceutical manufacturing.
• Language: Very good ability to communicate in both Swedish and English.

About the Company

Randstad

At Randstad, we know that everyone has a place in the job market. With operations across the country and in all areas of expertise, we help people find a job that feels right, where they can grow, develop, and reach their full potential.

With nearly 600,000 employees in 38 countries, Randstad is a world leader in HR services, aiming to be the world's leading and most appreciated partner in the job market. By combining our passion for people with the power of today's technology, we help individuals and companies achieve their full potential. We call it Human Forward.