Validation Engineer II/III (CSV) at Genezen

Lexington, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

17 Jun, 26

Salary

130000.0

Posted On

19 Mar, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Computer System Validation, Validation Plans, Test Validation Procedures, cGMP, Risk Assessments, Installation Qualification, Operational Qualification, Performance Qualification, Change Controls, Corrective and Preventative Actions, BMS, CMS, Automation Upgrades, Change Management, Data Integrity, GAMP 5

Industry

Biotechnology Research

Description

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 incumbent is responsible for assisting in completion of all computer system validation project milestones. This includes writing all validation deliverables within the Computer System Lifecycle, e.g. Validation Plans, Summary Reports, Configuration Specifications. Responsible for developing, revising test validation procedures/protocols, and preparation of all relevant documentation in accordance with appropriate regulatory agency validation requirements, quality management system and current industry practices (includes standard operating procedures, technical reports and risk assessments). ESSENTIAL JOB FUNCTIONS Develop moderately complex test protocols, provides on-site execution support, data analysis, and report generation for various installation, operational and performance qualification activities. Ensure performance of all qualification activities is in accordance with internal procedures, cGMP industry and regulatory guidance. Investigates / troubleshoots validation problems. Support and/or initiate investigations into protocol non-conformances and site deviations. Serve as initiator and owner of validation related change controls and corrective and preventative actions. Provides input to standard operating procedures related to validation practices. Support the implementation of validation programs (e.g., requalification). Represent the validation department at team meetings or projects. Performs periodic reviews and ongoing support of validated systems post Go-Live. Perform revalidation and change control validation related activities. Ability to apply complex system validation principles to work assignments. Responsible for executing and reviewing control systems validation activities including projects associated with BMS, CMS, and other automation upgrades. Assess the impact of system changes thru change management and change control systems; participate in the planning and implementation of change. Assist validation activities of cross functional teams that include technical functions such as Quality Control, Information Systems, Manufacturing and QA Engineering. SPECIAL WORK REQUIREMENTS Fully onsite position Adaptability required as work schedule may change based on business needs Criminal background check required Other duties as assigned EDUCATION/CERTIFCATIONS/LICENSES A minimum of a Bachelors degree in Engineering Essential ON-THE-JOB EXPERIENCE 5+ years of validation experience Essential KNOWLEDGE, SKILLS AND EXPERIENCE The individual must possess strong written and oral communication skills: The ability to communicate with employees of all experience levels. Essential The ability to report on project activity in a clear and concise manner. Essential The ability to negotiate when necessary and compromise with other project team representatives to achieve project goals. Essential The ability to listen and respect fellow project team member’s ideas and opinions and work through conflict and disagreements. Essential GMP compliance knowledge including knowledge of 21 CFR Parts 11, 210, 211, and 820 requirements, Data Integrity Guidance, ICH Q7A requirements, and GAMP 5. Essential Experience in thorough testing of applications, computerized systems, changes and implementations Essential Excellent written and oral communication to include accurate and legible documentation skills. Essential Ability to work independently in a fast-paced environment with a strong work ethic. Essential Must be able to sit or stand for prolonged periods of time. Essential Good knowledge and skills in engineering of Automation for HVAC/ Process Utility/Monitoring Building Management Systems. Essential Pay Range: The annual salary range for this position based upon level hired is: $90,000-$130,000 Work Environment Regularly sit for long periods of time 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 Rarely 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 Pay Range: The annual salary range for this position based upon level hired is: $85,000-$130,000 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.

Responsibilities

The incumbent is responsible for assisting in the completion of all computer system validation project milestones, including writing validation deliverables across the Computer System Lifecycle. Essential functions involve developing test protocols, providing execution support, data analysis, report generation for qualification activities, and troubleshooting validation problems.