Vacant job

Are you a team player who thrives in a fast-paced environment? Do you have experience/education in Quality Assurance and want to work with groundbreaking pharmaceutical manufacturing? Now you have the chance to become part of AstraZeneca in Södertälje through an exciting consultancy assignment (12 months) via KellyOCG!

Your Role

Organizationally, you belong to a group of about 50 people who support sterile manufacturing both in Snäckviken and Gärtuna.

You work closely with the exciting and dynamic production and are present “where it happens.” Daily, you participate in cross-functional discussions at the production line and make informed decisions on how production should proceed based on quality aspects. Approving protocols from manufacturing and thus being responsible for ensuring our products meet the required quality and standards is also part of your daily routine. The role often has an investigative nature where you gather facts and use your logical thinking to reach decisions. The work is independent and the tasks are broad, giving you a great opportunity for personal learning, and as a representative for your area, courage, commitment, determination, and integrity are essential.

We have close collaboration within our groups as well as with other support functions such as quality control, microbiology, process engineering, and maintenance, which places high demands on flexibility and good communication skills. Your position may be challenged, and you need to be able to justify your decisions effectively with both conviction and humility.

What Skills Are We Looking For?

• A scientific university or college degree of at least 240 credits including a course in microbiology of 7.5 credits.

• Excellent knowledge of Swedish and English, both spoken and written.

Examples of education include a Master’s degree in biotechnology, chemistry, or pharmaceuticals, or a pharmacy degree. It is advantageous if your education meets the competency requirements for Expert in LVFS 2004:7.

Experience in manufacturing, microbiology, quality control, quality assurance of pharmaceuticals, regulatory inspections, or validation/qualification is advantageous. Knowledge of LEAN is also beneficial. We would like you to have an interest in technology, systems, and processes.

To succeed in this role, you are a positive and solution-oriented person who enjoys a large network and broad collaboration across different functions. You are skilled at seeing the big picture and switching between long and short deadlines. You have the ability to communicate effectively and build trust, managing many interfaces and sometimes tough decisions with engagement and integrity.

Application deadline January 23, 2025.

Welcome to contribute to a team that makes a difference in other people's lives!