QC Lab Support (contractor)

QC Lab Support (Contractor)

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.

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 Lab Support Contractor plays a critical role in supporting day-to-day quality operations within the cGMP QC laboratories. This role is responsible for overseeing all aspects of GMP lab supply management, documentation and record keeping, lab equipment maintenance, reagent preparation and general lab support. In addition, individual will ensure compliance with documentation practices and contribute to maintaining an organized and efficient laboratory environment. This position is based at our state-of-the-art facility in Lexington, MA.

Essential Job Functions:

• GMP Supply Management: Ordering (Dynamics) Lab Supplies/Materials, Stocking and Inventory Management, Attend Tier 1 huddles.
• Documentation and Records Management: Create, manage, reconcile, scan and archival of QC controlled documentation, CFR 11 Retain management (annual inventory), Generate, Maintain, and Archive Equipment and system logbooks.
• Equipment Maintenance Support: Manage Pipet Calibration, Initiate general work order requests through Blue Mountain, Incubator/BSC Cleaning Support.
• General Lab Support and Reagent Preparation Support: Support general reagent buffer preparation, Support critical reagent aliquoting, Manage Chemical/Consumable Expiry, Support glass wash, Biohazardous Waste and Sharps Disposal, Support Lab Housekeeping, Support Sample Shipment.
• Additional Responsibilities: Perform other related duties as assigned by the supervisor or QC management.

Strong communication skills, Excellent organization abilities and attention to detail, Capability to work with minimal supervision, Ability to collaborate with diverse groups and manage multiple activities with challenging timelines, Criminal background check required, Other duties as assigned.

Knowledge, Skills and Experience

Education / Certifications / Licenses: BA or BS in Life Sciences, Essential

On-the-job Experience: 1-3 years of relevant GMP experience in a pharmaceutical/biotech company, with experience working within a quality system and regulated GMP environment.

Skills/Abilities: Understanding of documentation practices related to cGMP and data integrity, Proficiency in computer applications including MS Word, Excel, and LIMS (preferred), Strong communication and organizational skills, with the ability to work effectively both independently and as part of a team, Flexibility and willingness to learn, with a proactive approach to making a positive impact.

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.

Movement: Frequently required to stand; sit; reach with hands and arms, lift from a cryo-tank or -80C freezer, Occasionally required to walk and push a cart.

Lifting: Ability to lift and/or move up to 25 pounds.

Vision: Vision test required.

Communication: Frequently required to communicate by talking, hearing, using teams and email.

Pay Range: This is a temporary position paid through a third party payrolling service. The hourly pay rate for the role is $30-$38/hr.

Genezen's 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 principles.

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 operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts.