EQRx believes responsibility can be revolutionary. Want to make a difference while advancing your career? Come join a team that is working towards our bold mission of developing innovative medicines at radically low prices to help people get the medicines they need.

Who We Are:

We're a new kind of biotech, one with a bold mission to bring innovative new medicines at dramatically lower costs.

What You’ll Do:

As Senior Manager of Regulatory Operations, you’ll play a key role in our highly dynamic organization. You will oversee the end-to-end submission execution activities including, planning/scheduling, publishing, QC and dispatch/transmit our regulatory submissions to health authorities per guidance and will participate in the building of a Best-in-Class Regulatory Operations team.

You will be responsible for the development of country specific submission requirements manuals and maintenance based on industry and country requirement changes. To support these efforts, you’ll need to monitor changes in regulations and guidelines for submission publishing impact, participate in industry engagements, disseminate relevant changes in regulations and guidance to affected parties and design and direct implementation of training as required to support changes. You will serve as a SME (subject matter expert) to submission filing teams to ensure filing excellence.

You will develop global strategic plans to support current and future health authorities’ submission requirements to apply consistency for all EQRx submission publishing standards and processes. You will also assist in developing, implementing, and communicating the Global Regulatory Operations vision, metrics, budget activities, core capabilities, process improvements and value while championing a strong Submission Excellence Culture.

The Impact You Will Have:

This is not your standard Regulatory Operations position. We are doing things different here than how it is normally done, and this role is no exception. This position is highly visible and of significant impact to the company. We are on a critical mission to bring quality solutions to patients at a fraction of the price. This role will help us drive forward towards that pinnacle goal of truly putting patients first.

Your Professional Superpowers:

• You have a bachelor’s degree
• You have 5+ years of related pharmaceutical/biotechnology industry experience, with 3+ years within Regulatory Operations and a thorough understanding of process and technology solutions.
• You’ve supported at least one successful major electronic application (NDA, BLA, MAA, JNDA, etc.).
• You have successfully managed submissions in Veeva RIM in an organization that has embraced the Veeva Platform as the master document management system, where cross functional system alignment is essential.
• You endeavor to interface with relevant associations and external groups to increase the company’s ability to influence a changing regulatory informatics environment.
• You can thrive in a smaller company environment and love the pace of a fast-growing company.
• You understand relationships are key and have strong interpersonal skills.
• You can work both independently with minimal direction and collaboratively. within the Regulatory Affairs team and across multi-stakeholder teams.
• You’re a team player who is willing to roll-up your sleeves and get the job done.
• You can work effectively on multiple global programs in a fast-paced environment.

Are you bold enough?

Your work should matter and allow you the freedom to be 100% you. We spend too much time and effort in our career to not feel excited and proud about what we do and who we do it with. In other words, your career is too important for your next move to be just another job, so let’s work together to change the world and bring affordable medicines to all patients.

We aren’t about a bunch of empty slogans on a wall or words on a coffee cup – you can find that in lots of places. We are a culture of individuals with diverse backgrounds and personalities.