QC Analyst Contract

Job Description

Job Description

QC Analyst – Contract

Location: Winston-Salem, NC
Pay: $28–$35/hour , depending on experience
100% Onsite | GMP/GLP Regulated Environment
Contract Position

We’re seeking an experienced QC Analyst to support Quality Control operations within a growing pharmaceutical/biotechnology manufacturing environment. This role is ideal for a hands-on laboratory professional with 3–5+ years of relevant experience who is comfortable working in GMP-regulated environments and supporting environmental monitoring, QC testing, documentation, and laboratory operations.

What You'll Do

• Perform routine Environmental Monitoring (EM) of cleanrooms, Cell Processing Units, facilities, and QC equipment
• Set up and operate QC laboratory equipment including cell counters, centrifuges, and analytical balances
• Handle and coordinate QC samples for release testing
• Execute approved protocols and support process development activities
• Collect, compile, and maintain data from QC testing and Environmental Monitoring
• Complete GMP documentation, testing forms, logbooks, and other quality records in accordance with Good Documentation Practices (GDP)
• Follow SOPs, GLP, cGMP requirements, safety procedures, and established QC schedules
• Support the revision of SOPs, testing forms, and other controlled documents
• Monitor QC laboratory and manufacturing-area inventory and coordinate material requests
• Process material and purchase requisitions through ERP systems
• Support training and onboarding of new QC personnel
• Work closely with Quality Assurance and Senior QC Analysts
• Recognize and appropriately report deviations from established procedures
• Procure and coordinate dry ice for clinical sample shipments when required
• Travel between company facilities as needed

What We're Looking For

• Bachelor’s degree in Microbiology, Biology, Chemistry, or another science-related field
• 3–5+ years of relevant laboratory/QC experience
• Experience working in a GMP-regulated pharmaceutical, biotech, or manufacturing environment
• Working knowledge of:
  • cGMP
  • SOPs
  • QC testing and documentation
  • Environmental Monitoring
• Strong attention to detail and documentation practices
• Ability to follow established procedures while recognizing and escalating issues
• Comfortable working independently and collaboratively in a fast-paced environment
• Strong organizational, communication, and time-management skills
• Proficiency with Microsoft Office
• Good laboratory/hand-eye coordination and ability to perform hands-on laboratory activities

Why Consider This Opportunity?

This is a great opportunity for a QC professional looking to gain or expand experience in a highly regulated pharmaceutical/biotech environment , with exposure to Environmental Monitoring, QC operations, GMP documentation, protocol execution, and manufacturing support.

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Please note: The following benefits reflect Kelly's general offerings. Eligibility may vary by assignment, location, and job type. 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 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.

Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly 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. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.