From Genezen's posting. “We” and “our” refer to the employer.
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 Senior Manager/Associate Direct, Analytical Development & Quality Control provides scientific, and operational leadership for analytical development and QC functions supporting viral vector programs (AAV, LVV, RVV). This role is accountable for integrating Analytical Development and Quality Control into a unified, phase-appropriate analytical lifecycle that supports both scientific innovation and GMP execution.
This role is responsible for coordinating phase-appropriate analytical lifecycle activities that support method development, GMP execution, regulatory readiness, and data integrity.
This role partners across Analytical Development, Quality Control, Quality Assurance, Regulatory Affairs, Manufacturing, and Process Development to ensure analytical activities are aligned with program needs, GMP expectations, and inspection readiness requirements
ESSENTIAL JOB FUNCTIONS
Analytical Development & Lifecycle Management
Manage and support analytical method development, qualification, validation, transfer, and lifecycle activities in alignment with ICH Q2/Q10/Q14 principles and program requirements.
Implement and maintain method transfer processes, including acceptance criteria, readiness assessments, documentation, and ongoing performance monitoring.
Contribute to the development and optimization of analytical platforms and reference standards supporting viral vector characterization.
Support development and execution of sampling strategies to ensure representative, compliant testing and clear alignment with program and quality requirements.
Quality Control Operations & Stability
Lead QC laboratory operations supporting in-process, release, and stability testing.
Provide technical decision authority for analytical readiness, method suitability, and QC support of batch disposition.
Oversee stability strategies, including protocol design, trending, and shelf-life justification.
Direct investigations (OOS, OOT, deviations) and ensure effective CAPA implementation.
Ensure QC operations maintain appropriate independence and objectivity in support of quality decisions.
Laboratory & Shared Infrastructure Governance
Own governance of shared laboratory infrastructure, including equipment lifecycle management, scheduling prioritization, and resource allocation.
Ensure appropriate segregation and controls for GMP and non-GMP activities within shared laboratory spaces.
Microbiology, EM & Contamination Control
Serve as SME for aseptic processing, contamination control, and microbiological monitoring.
Oversee environmental monitoring programs, trending, and control strategies.
Ensure microbiological controls support product quality and regulatory compliance.
Regulatory Compliance & Inspection Readiness
Ensure compliance with cGMP, GLP, FDA, EMA, and applicable regulatory requirements.
Serve as primary SME during regulatory inspections and client audits for analytical and QC functions.
Support regulatory filings, responses, and analytical justification strategies.
Maintain continuous inspection readiness across laboratory operations.
Data Integrity, Systems & Continuous Improvement
Oversee LIMS, analytical systems, and data integrity (ALCOA+, Part 11) across all laboratory functions.
Implement digital solutions, automation, and process improvements to enhance efficiency and compliance.
Establish and monitor performance metrics (e.g., turnaround time, right-first-time, deviation trends).
Client & Cross-Functional Leadership
Act as executive scientific partner for clients and internal stakeholders.
Drive alignment across Process Development, Manufacturing, QA, and RA on analytical strategy and readiness.
Support proposals, scope definition, and client program execution.
Lead analytical aspects of technology transfer and commercialization.
Organizational Leadership
Lead a hybrid organization with direct oversight of QC and indirect leadership of AD via scientific leads.
Build and develop high-performing teams through coaching, performance management, and succession planning.
Establish a culture of scientific excellence, accountability, and continuous improvement.
KNOWLEDGE, SKILLS, AND EXPERIENCE
EDUCATION / CERTIFICATIONS / LICENSES
Essential/Desired
BS in Molecular Biology, Biochemistry, Chemistry or related field
Essential
MS in Molecular Biology, Biochemistry, Chemistry or related field
Desired
ON-THE-JOB EXPERIENCE
Minimum 4 years in a leadership role
Essential
Minimum 8 - 10 years progressive experience in analytical development, quality control, or related discipline within biopharma or CDMO environments
Essential
Extensive experience supporting viral vector products across clinical development phases and regulatory submissions
Essential
Demonstrated success leading analytical development, method validation, and QC Operations in a cGMP environment
Essential
SKILLS / ABILITIES
Strong understanding of analytical methods used for viral vector characterization including:
qPCR and ddPCR
ELISA
Flow cytometry
Cell-based potency assays
Genome integrity assays
Empty/full capsid analysis
Essential
Extensive knowledge of cGMP, GLP, FDA, EMA, and ICH requirements.
Essential
Excellent communication skills and ability to thrive in fast paced, dynamic environment
Essential
Experience with environmental monitoring programs, contamination control, and aseptic manufacturing support.
Essential
Familiarity with laboratory systems, LIMS, data integrity principles, and automation technologies.
Essential
Proven leadership experience, with a track record of building and managing high-performing teams
Essential
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
Spending time on the floor during activity execution (maintenance, construction, commissioning and qualification) is required
Movement
Frequently required to stand; sit; 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 10 pounds
Occasionally lift and/or move up to 25 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
C ommitted to Science
We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.
U rgency in action for the patients
We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.
R esilience & Grit in operations
We are committed to overcoming challenges, learning from failures, and persistently striving for success.
E xecute with Excellence & Integrity
We are dedicated to delivering quality results and upholding ethical principals.
S olutions driven for our partners
We are committed to being a proactive, collaborative, creative and open-minded partner.
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.
About this listing
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