Stability Manager, Quality Control

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures.  WORKING AT GENEZEN Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team. JOB SUMMARY The Quality Control Technical Services (QCTS) team manages the lifecycle of analytical methods, including method transfer and validation, stability programs, reference standards, critical reagents, product specifications, and computer systems validation. The Manager, QC Stability provides leadership and strategic oversight of the stability programs from early phase through commercialized programs. This role ensures regulatory compliance, analytical excellence, and effective cross-functional collaboration to maintain product quality throughout the product lifecycle ESSENTIAL JOB FUNCTIONS  Govern the Stability Program on behalf of clients across all early phase, and commercial programs for DS, DP, and diluents  Ensure compliance with Quality Agreements and global regulatory expectations  Maintain and oversee the Stability Master Planner  Monitor and publish stability KPIs  Supervise, mentor, and develop team members.  Own quality documentation including deviations, CAPAs, and change controls related to stability  Manage the revision and approval SOPs, protocols, and reports  Conduct audits of stability studies and processes  Verify data for accuracy and compliance  Summarize and interpret stability data and generate stability trend analysis reports  Partner with cross-functional teams for execution of stability studies  Identify and implement operational improvements  SPECIAL JOB REQUIREMENTS Proven leadership and cross-functional collaboration skills  Ability to manage competing priorities under pressure  Highly organized with strong problem-solving skills  Clear professional communication and presentation skills  Commitment to quality, integrity, and continuous improvement  Prior CDMO experience a plus  Adaptability required as work schedule may change based on business needs Criminal background check required Other duties as assigned EDUCATION Education Level: Master’s Degree in science-related field ON-THE-JOB EXPERIENCE 8+ years of industry experience in CDMO  Experience managing stability programs for cell/gene therapy products  Strong understanding of cGMPs and global regulations  Experience managing deviations, CAPAs, and change controls  Experience with analytical methods such as potency assays, ELISA, ddPCR, qPCR, SEC-HPLC, and CE-SDS    SKILLS/ABILITIES Prior experience working in a CDMO environment  8+ years working in a Good Manufacturing Practices (GMP) environment  Subject matter expert in Good Documentation Practices (GDP)  Excellent computer literacy (MS Word, Excel, SmartSheets)  Excellent project management tools (MS project, SmartSheets)  Excellent executive communication skills, both written and oral  PAY RANGE: The annual salary range for this position is $130,000-$150,000. PHYSICAL DEMANDS  While performing the duties of this job, the employee is required to meet the following physical demands: Work Environment Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock Occasionally exposed to extremely loud noise levels Regularly sit for long periods of time Movement Frequently required to stand; sit; walk; balance; stoop; kneel; crouch; use hands to finger, handle, or feel; reach with hands and arms Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl Lifting Frequently lift and/or move up to 25 pounds Occasionally lift and/or move up to 50 pounds Vision Frequently utilize close vision and the ability to adjust focus Communication Frequently required to communicate by talking, hearing, using telephone and e-mail  GENEZEN'S CURES VALUE-BASED COMPETENCIES Committed to Science We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare. Urgency in action for the patients We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs. Resilience & Grit in operations We are committed to overcoming challenges, learning from failures, and persistently striving for success.  Execute with Excellence & Integrity We are dedicated to delivering quality results and upholding ethical principals. Solutions driven for our partners We are committed to being a proactive, collaborative, creative and open-minded partner. GENEZEN'S BENEFITS Paid vacation days, amount based on tenure Paid sick time 10 observed holidays + 2 floating holiday + 1 volunteer day 401(k) plan with company match up to 6% of salary, vested immediately Share Appreciation Rights Choice of several healthcare plans FSA and HSA programs Dental & vision care Employer-paid basic term life/personal accident insurance Voluntary disability, universal life/personal accident insurance Accidental Death & Dismemberment (AD&D) Insurance ADDITIONAL DETAILS Nothing in the job description for this role restricts management’s right to assign or reassign duties and responsibilities to this job at any time. This position requires a criminal background check. Genezen is an Equal Opportunity Employer. Genezen participates in EVerify. Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas. Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts.  Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world’s largest children’s museum--to name just a few reasons why this area is a great place to live. Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride. Offices: Lexington, Massachusetts, United States (Massachusetts);