Vacant job

Are you interested in working in Quality Assurance (QA) or Quality Control (QC) within an international pharmaceutical organization? For our partner AstraZeneca, we at KellyOCG are continuously looking for dedicated consultants who want to help ensure that medicines meet the highest quality and safety standards for patients worldwide.

About the assignments

As a consultant through KellyOCG, you will become part of AstraZeneca's organization and work closely with operations in Södertälje. The assignments vary in scope and focus, but they all share a central role in supporting manufacturing, development, or quality systems – always with a focus on GMP and regulatory requirements.

Examples of tasks

• Review, release, and quality assurance of manufactured products or raw materials
• Participation in investigations of deviations, changes, and improvement work
• Quality control of active pharmaceutical ingredients and finished products
• Contribute to cross-functional projects related to processes, validations, or inspections

Requirements

• Scientific university or college degree (e.g., pharmacist, engineer, biotechnology, chemistry, or similar)
• Experience working in the pharmaceutical industry, QA, or QC
• Knowledge of pharmaceutical manufacturing according to applicable regulations and GMP
• Good knowledge of Swedish and English, both spoken and written

Meritorious

• Experience from manufacturing, laboratory work, quality review, or regulatory inspections
• Knowledge in LEAN, validation/qualification, or improvement work
• Interest in digital processes and systems

About KellyOCG

As a consultant through KellyOCG, you will be an important part of our operations while being fully integrated into AstraZeneca's team. We offer secure employment conditions, collective agreements, and the opportunity to develop in a global environment where your work makes a difference for patients worldwide.

Are you interested in future assignments in QA or QC at AstraZeneca? Please submit your application today!