Quality Assurance Associate at Astra Zeneca

At our client Astra Zeneca, you have the opportunity to work in an innovative environment where your commitment helps create life-changing medicines. Every day is a chance to take initiative, collaborate with experts, and develop in a dynamic production environment. Be part of something great.

About the position

As a Quality Assurance Associate, you will work closely with production, participate in cross-functional discussions, and make decisions regarding production quality. You will be responsible for approving manufacturing protocols and ensuring that products meet requirements. The role involves independent investigative work where you apply logical thinking. You will have opportunities for learning and need courage, commitment, determination, and integrity.

Within QA OSD, we participate in projects such as NPI, investment projects, and Tech Transfer, as well as projects with external customers and improvement efforts. We collaborate closely with production and support functions, which requires flexibility and good communication skills. You need to justify your decisions with both conviction and humility.

About you

We are looking for a driven, solution-oriented person who enjoys making changes – big and small. You thrive with a large network, can meet the diverse needs of multiple customers while prioritizing your own work. You have the ability to communicate effectively and build trust, managing many contact points and sometimes tough decisions with engagement and integrity. Your drive and ability to work both meticulously and structured even at a high pace will help you succeed.

Formal qualifications

• A scientific university degree of at least 4 years, preferably with a focus on biotechnology, chemistry, or pharmaceuticals, or a pharmacy degree.
• You need to have good knowledge of pharmaceutical manufacturing according to applicable regulations and Good Manufacturing Practice (GMP).
• Excellent knowledge of Swedish and English, both spoken and written.

Meritorious

It is an advantage if you have experience in pharmaceutical manufacturing, quality control, quality assurance, regulatory inspections, or validation/qualification. Knowledge of LEAN is also beneficial. We prefer candidates with an interest in technology, systems, and processes. Experience working with various customer needs and communicating effectively in a dynamic work environment is valuable for this role. Your ability to handle challenges with commitment can contribute to your success with us.

As one of us

As an employee staffing consultant with us, you will always receive a competitive salary, vacation, pension contributions, insurance, and access to our collective agreement. We want you to feel good with us, so we naturally offer our consultants wellness benefits and occupational health care. During your employment, you will have a consulting manager responsible for your assignment, ensuring that you thrive in your workplace, supporting you, and helping you develop in your professional role.

About Lernia

Lernia is one of Sweden's leading staffing and recruitment companies and operates nationwide. With our extensive network, we offer exciting jobs with attractive employers and brands that help you develop your skills and career, both in the long and short term.

How to apply for the position

To apply for the position, scroll down to the application form below. Selection and interviews are ongoing, so submit your application today! If you have any questions, feel free to contact consulting manager Hanna Bertilsson via email: hanna.bertilsson@lernia.se (mailto:hanna.bertilsson@lernia.se). Welcome to apply for this position by sending your CV and cover letter via the link.