# GxP Quality Associate Returnship **Company**: Recursion **Location**: Salt Lake City, Utah **Work arrangement**: hybrid **Experience**: senior **Job type**: full-time **Category**: Operations **Industry**: Healthcare **Apply**: https://job-boards.greenhouse.io/recursionpharmaceuticals/jobs/8380698?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply **Canonical**: https://yubhub.co/job/gxp-quality-associate-returnship-2974bf6b-826/ ## Description ## 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. For more fresh new jobs, check out [yubhub.co](https://yubhub.co/). ## Skills ### Required - GxP - Good Documentation Practices - data integrity - ALCOA+ - GxP data and document standards - eQMS ### Nice to have - GCP - GMP - GLP - CSV/CSA - 21 CFR Part 11 --- Source: [Apply at job-boards.greenhouse.io](https://job-boards.greenhouse.io/recursionpharmaceuticals/jobs/8380698?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)