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Senior Quality Control Analyst (Microbiology) – Contract

**Location:** Gaithersburg, MD (On-site)

**Schedule:** Monday–Friday, 8:00 AM – 5:00 PM (occasional weekends)

**Duration:** 3 months

**Pay Rate:** $47–$50 per hour

**Start Date:** ASAP

About the Role

We are seeking a **Senior Quality Control Analyst (Microbiology)** to support microbiology programs focused on **lentiviral vector and cell & gene therapy** development. The ideal candidate will have hands-on experience in a **cGMP microbiology quality control environment** , strong technical acumen, and the ability to work independently with minimal supervision.

This role plays a key part in ensuring product quality and compliance with internal procedures and regulatory standards (ICH, CFR, etc.).

Key Responsibilities

+ Execute day-to-day microbiology testing and related activities with minimal supervision.

+ Apply sound scientific and technical judgment to ensure accuracy and reliability of results.

+ Conduct and write investigations, reports, and deviations independently or with limited assistance.

+ Identify and support resolution of out-of-trend (OOT) and out-of-specification (OOS) events.

+ Contribute to the improvement of existing procedures and development of new laboratory processes.

+ Coordinate sample shipments, contract laboratory testing, and equipment maintenance.

+ Maintain and track microbiological data and metrics for management review.

+ Ensure compliance with all cGMP, internal, and regulatory guidelines.

Required Qualifications

+ **Bachelor’s (B.S.) or Master’s (M.S.) degree** in Biotechnology, Biology, Chemistry, or a related field.

+ **5+ years** of hands-on experience in a **cGMP microbiology QC laboratory** within the biotech or pharmaceutical industry.

+ Strong understanding of **aseptic technique** , **product sample handling** , and **microorganism culture** .

+ Proven ability to **write and support technical documentation** , including SOPs, protocols, and investigations.

+ Excellent **attention to detail** , **organizational** , and **problem-solving** skills.

+ Strong communication abilities—both written and verbal—and experience collaborating with cross-functional teams.

+ Proficiency with **Microsoft Office applications** (Excel, Word, PowerPoint, Outlook).

Preferred Experience

+ Prior experience supporting **cell and gene therapy programs** or **lentiviral vector manufacturing** .

+ Familiarity with **ICH and CFR regulatory guidance** .

+ Demonstrated ability to manage multiple priorities in a fast-paced, highly regulated environment.

Important Note

This role requires **industry experience** —candidates with **academic or NIH backgrounds only** will not be considered. Hands-on biotech or pharmaceutical experience is essential.

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As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (https://www.mykelly.com/help-support-working-with-kelly-us/#Benefits) for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly ® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.

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Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly’s Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.