Team Photograph: Photograph for Associate Director, Analytical Quality

We believe it’s possible to have a profound impact on bending the cost curve in healthcare by building a pipeline of innovative medicines and bringing them to market at dramatically lower prices.

Robert Forrester CXO

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:

You will lead the Analytical Quality effort including reviews of drug substance and drug product analytical methods, analytical method validations, and analytical data records in support of product disposition of API and finished goods for both small molecules and biologics. You will lead the EQRx stability program for all commercial products and provide oversight of the stability program for the clinical products through will review/approval of stability protocols, analytical data, and reports from contract laboratories and contract manufacturing sites. You will contribute to vendor management programs by evaluating questionnaires, audit reports and risk assessment documents for analytical laboratories. You will lead the quality review of CMC analytical sections in regulatory applications and function in a supporting role during partner due diligence activities and regulatory inspections.

The Impact You Will Have:

Every hire here is critical to our success. EQRx is an organization whose success is fundamentally tied to high quality products, and you will be the major driver in ensuring our analytical methods and testing are of the highest caliber. You will also lead the development of our stability program ensuring our products maintain their high quality throughout their shelf life.

Your Professional Superpowers:

  • You have a BA/BS in a scientific discipline with a minimum of 8 years of relevant experience in a regulated environment with at least 6 years focused on analytical quality.
  • You have strong knowledge of global cGMP & GLP regulations and guidance with a working knowledge of ICH/GxP regulations and expectations.
  • You have experience working with Contract Testing Laboratories.
  • You have strong technical expertise in QA/QC processes supporting development and maintenance of cGMP compliant quality systems for API and finished product analytical testing, preferably in both biologics and small molecules.
  • You can participate and work effectively on multiple cross-functional teams.
  • You play well in the sandbox. You understand relationships are key and have strong interpersonal skills.
  • You are a leader. Teams love working with you and you are someone who takes pride in mentoring and supporting the careers of others.
  • You’re a team player who is willing to roll-up your sleeves and get the job done.

Apply

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.

The Champion

Are you ready to build a sustainable pipeline of excellent drugs at much lower prices?

  • Attribute Thumbnail: Self-Awareness Self-Awareness
  • Attribute Thumbnail: Accountability Accountability
  • Attribute Thumbnail: Communication Communication
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What does EQRx stand for?

  • EQuality Medicines: Equally good or better, innovative medicines
  • EQuitable Medicines: Making innovative medicines affordable
  • EQual Access: Sustainable, frictionless access for people to cutting-edge medicines

We have a bold mission and are looking for equally bold people who want to join us and help make a difference in the world. If you want to grease the wheel we are definitely not for you. Want to build the wheel? We might be just what you are looking for.

EQRx is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

It’s (mutually) beneficial.

You’re curious about what sets us apart from the rest. What do you get from working at EQRx?

So, let’s start big—working at EQRx means having the opportunity to change the world.

By joining a team that’s remaking medicine development from start to finish, you’re going to enjoy the daily rush of throwing caution to the wind and doing things differently by:

  • Working with the smartest game-changers in the industry
  • Cutting down the red tape of “the way things are done”
  • Seeing and feeling the daily impact of your work
  • Growing as a professional and a person
  • Committing to neverending social responsibility

And, yes—we also have a killer list of things that’ll help you shine as part of the team.

But to us, these are just table stakes.

  • 100% Medical, Dental, and Vision coverage
  • Flexible Spending Account
  • Health Reimbursement Account
  • Free snacks and drinks

*As EQRx grows, please note that some of these are subject to change.

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