Do you have expertise in regulatory and overall understanding of Gx P requirements? Are you highly collaborative and like contributing to clear instructions and implementing process improvements? This opportunity as Processes Specialist in the Regulatory Process and Compliance team might be the right opportunity for you.
For our close partner Astra Zeneca, Kelly OCG is seeking a Operations Regulatory CMC - Specialist for a contract on 8 months. You will work entirely onsite at Astra Zeneca in Gothenburg / Mölndal, becoming an integral part of their team and reporting directly to their manager.
At Astra Zeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means putting patients first, doing the right thing and working together to make the impossible a reality. If you are swift to action, willing to collaborate, and curious about what science can do, then you’re our kind of person. Global Regulatory Excellence’s vision is to Leading enterprise-wide regulatory strategies, policy and delivery - so that no patient waits. In the Regulatory Process and Compliance team we network collaboratively to enable our customer groups to operate efficient processes in a compliant manner.
What you’ll do
As a Processes Specialist in the Regulatory Process and Compliance team you will be working with the Process team members and taking responsibility for the management of assigned tasks related to procedural document management. You will act as technical writer and reviewer, and support project management to ongoing procedural document update program.
You will be accountable to execute the delivery of the authoring and lifecycle management of current procedural documents. We hope that you have the drive to establish a culture of continuous improvement, high performance, flexibility and quality, emphasizing a “can do” attitude and ensuring high standards of quality in all outputs.

Other key responsibilities in this position:

• Identify opportunities for and drives the enhancement of existing processes and procedural documents
• Using understanding of regulatory processes and regulations to provide support to regulatory process team
• Identify opportunities to improve and simplify the methodology in processes and guidance, provide practical solutions
• Review and verify documents and data for accuracy and completeness
• Collaborate with team members to ensure high standards of quality in all outputs
• Contribute to communication and change management activities associated with process initiatives

The final application date is December 12th, but we encourage early applications as positions may be filled before the deadline. We will review applications and conduct interviews on a rolling basis.
Does this sound like your next challenge? Apply today!