GxP Quality Associate Returnship

Job Summary

We are Recursion, a clinical-stage TechBio company, and we're building a future where biology is solvable. Our goal is to radically improve lives by accelerating the development of life-changing treatments.

Recursion’s Returnship Program

Recursion’s Returnship program, sponsored by the Women at Recursion Employee Resource Group, helps professionals who have taken a break of two or more years from the STEM industry return to the workforce. Participants work in a supportive, learning-focused environment with guidance from their teams and mentors.

What You’ll Get

• A dedicated mentor who meets with you weekly
• Weekly seminars on workplace culture, communication, and technology
• Support from your team as you re-enter the workforce

Program Details

Our program runs for sixteen weeks, from March 2027 through the end of June 2027. Depending on performance and business needs, it may lead to full-time employment. This position is primarily based at our Salt Lake City, UT headquarters, with some hybrid flexibility.

GxP Quality Associate Returnship

As a GxP Quality Associate, you will report directly to the Quality team's hiring manager and be paired with a dedicated mentor. You'll work closely with the Quality team and cross-functional partners. We are looking for someone who is detail-oriented and organized, communicates clearly, and wants to learn new tools and systems in a fast-paced environment.

Responsibilities

• QC GxP documents and records for completeness, accuracy and compliance with Good Documentation Practices and data integrity principles (ALCOA+).
• Support GxP data migrations by loading data and verifying that migrated data and documents are complete, accurate and traceable.
• Standardize procedures by converting existing documents into a standard template for use in our electronic Quality Management System (eQMS).
• Help teams connect data and documents across systems so records are organized, findable and inspection-ready.
• Partner with teams across Recursion to answer documentation questions and support consistent quality practices.
• Learn our eQMS and GxP systems and the processes that keep them compliant.

Requirements

• 5–10 years of experience working in a GxP-regulated environment, preferably GCP. GMP, GLP and CSV/CSA experience are also valued.
• Bachelor's degree in a scientific or technical field, or equivalent job experience and relevant certifications or training.
• Familiarity with GxP data and document standards, such as Good Documentation Practices and ALCOA+.
• Must have taken a 2+ year break from full-time, industry-relevant employment just prior to the program start.
• Must be a Utah resident.
• A strong desire to learn, with excellent written and verbal communication skills.
• Strong attention to detail and the ability to accurately review and record information.
• Enjoys working both independently and collaboratively with cross-functional teams.

Values

• We act boldly with integrity.
• We care deeply and engage directly.
• We learn actively and adapt rapidly.
• We move with urgency because patients are waiting.
• We take ownership and accountability.
• We are One Recursion.