QC Technical Services Associate

Posted 3 Days Ago
Be an Early Applicant
Lexington, MA
Junior
Biotech
The Role
The QC Technical Services Associate supports stability and critical reagents within QC, authors SOPs, verifies data, and collaborates with QC Operations and Assurance.
Summary Generated by Built In

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 QC Technical Services Associate will be supporting key stability and critical reagents within the Quality Control Technical Services department at the Lexington MA facilityThis individual will work collaboratively with QC Operations, Analytical Development, and Quality Assurance in support of clinical pipeline and commercial products. This position will report directly to the QCTS Scientist. 

ESSENTIAL JOB FUNCTIONS

  • Work under general guidance to support Genezen’s programs, from early phase to commercialization.
  • Support and own quality documentation, including Change Control and CAPA.
  • Will provide data verification of QC results.
  • Create, implement and support data tables, and assay and/or sample trending.
  • Working knowledge of quality system requirements.
  • Complete documentation in accordance with current Good Manufacturing Practices (cGMP).
  • Will author and revise Standard Operating Procedures (SOPs).  

SPECIAL JOB REQUIREMENTS

  • Criminal background check required
  • Other duties as assigned

KNOWLEDGE, SKILLS AND EXPERIENCE

EDUCATION / CERTIFICATIONS / LICENSES

Essential/Desired

BS in Life Sciences or Engineering

Essential

ON-THE-JOB EXPERIENCE

 

2-3 years of QC laboratory experience in a cGMP environment

Desired

Experience in Quality Control within the biological pharmaceutical industry.  

Essential

Proficiency in writing SOPs, qualifications protocols, and reports. 

Essential

Working knowledge of quality system requirements. 

Essential

SKILLS / ABILITIES

 

Excellent analytical and problem-solving skills 

Essential

Must possess excellent communication and organizational skills 

Essential

Cross functional collaboration ability to work well with diverse groups 

Essential

Proficient in using Microsoft applications (MS Word, MS Excel, MS PowerPoint) 

Essential

Effective oral and written communication skills 

Essential

Confident, independent, self-starter, proactive, and results-oriented with high performance and compliance standards 

Essential

Exhibits highest integrity and committed to ethics and compliance standards 

Essential

Open and transparent in sharing data and information 

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

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.

Top Skills

Microsoft Applications (Ms Word
Excel
Ms Powerpoint)
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The Company
HQ: Indianapolis, IN
55 Employees
On-site Workplace
Year Founded: 2014

What We Do

Founded in Indianapolis in 2014, Genezen is focused on supporting the demands of the current and future gene and cell therapy manufacturing market worldwide— making viral vector production accessible to both early-stage, growth-oriented companies and established industry leaders. Genezen offers early-phase process development, GMP lentiviral vector production, retroviral vector production, and analytical testing services, building on the company's expansive knowledge and experience in the industry and working with the nation's leading institutions. For more information, or to learn more about services offered in Genezen's new cGMP facility, please visit our website: www.genezen.com

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