Validation Engineer II/III

Genezen; Indianapolis (IN); On-site; USD 85,000 - 110,000; Full time

Job summary

A leading company in gene therapy is seeking a Validation Engineer II/III to assist in project milestones and manufacturing support. The role involves protocol generation, qualification activities, and ensuring compliance with regulatory requirements. Ideal candidates will have a Bachelor's degree in Engineering and 5-8 years of validation experience. Join a collaborative environment focused on innovation and quality.

Benefits

Paid vacation days

Paid sick time

401(k) plan with company match

Choice of several healthcare plans

Dental & vision care

Qualifications

• 5-8 years of validation experience required.
• Ability to manage multiple activities with challenging timelines.

Responsibilities

• Assist in completion of project milestones and manufacturing support.
• Support investigations into protocol nonconformances.

Skills

Communication

Technical writing

Understanding of cGMP regulations

Education

Bachelors degree in Engineering

Tools

Microsoft Office

Excel

Visio

Job description

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Validation Engineer II/III

Lexington, MA

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 the Validation Manger in completion of all project milestones as well as manufacturing support. This includes performance qualification of equipment and utilities, environmental qualification, process transfer and scale-up, process validation, preparation of cGMP materials and preparation of all relevant documentation to meet regulatory requirements for new and existing products (includes standard operating procedures, technical reports and risk assessments).

ESSENTIAL JOB FUNCTIONS

• Protocol generation, execution support, data analysis, report generation and approval for various installation, operational and performance qualification activities
• Review and approve qualification documentation on behalf of the validation department.
• Ensure performance of all qualification activities is in accordance with local procedures, industry and regulatory guidance.
• Support investigations into protocol nonconformances and site deviations.
• Serve as initiator and owner of validation related change controls and corrective and preventative actions.
• Author standard operating procedures related to validation practices.
• Support the execution and generation of formal risk assessments.
• Support the generation and implementation of validation programs.
• Experience working in clean rooms.
• Experience with aseptic fill finish technique.
  
  

SPECIAL WORK REQUIREMENTS

• 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

Desired

ON-THE-JOB EXPERIENCE

5-8 years of validation experience

Desired

KNOWLEDGE, SKILLS AND EXPERIENCE

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 communicate with fellow project team members

Essential

Understanding of cGMP regulations

Essential

Technical writing ability

Essential

Familiarity with Microsoft Office, Excel, and Visio

Essential

Ability to work well with diverse groups in a matrix-style, growing, safety focused organization

Essential

Ability to manage multiple activities with challenging timelines

Essential

Able to access crawl spaces and use ladders to access equipment.

Essential

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
  
  

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.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

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