Quality Release Technician

Job Description

Job Description

Quality Release Technician

Location: Cornelia, GA
Pay: $21–$25/hour
Schedule: Tuesday–Saturday, 12:00 PM–8:00 PM after training
Training: 1 week onsite NEO, followed by approximately 2 weeks of Monday–Friday, 1st-shift training (details to be confirmed)
Contract: Long-term contract
Travel: Approximately 2x/month to Athens, GA
Employment Type: Contract, Non-Exempt / Hourly
Industry: Pharmaceutical / Healthcare Manufacturing
Focus: Quality Control | GMP | Batch & Product Release

About the Opportunity

Kelly Science & Clinical is seeking a  Quality Release Technician to support the Quality Control organization of a leading global healthcare and pharmaceutical company in Cornelia, GA. This role is ideal for an early-career science or technology professional interested in  GMP, quality control, laboratory operations, and finished-product release .

The Quality Release Technician will support day-to-day quality activities, including reviewing production batch records, completing lot release documentation, maintaining quality records, and supporting the release of finished goods for distribution.

About the Company

Our client is a leading global healthcare company with a broad portfolio of pharmaceutical, medical device, and health-related products. The organization is committed to improving patient outcomes through science, innovation, and high-quality manufacturing practices. This position offers the opportunity to contribute to a regulated manufacturing environment where quality, compliance, and attention to detail are critical.

Responsibilities

• Review production batch records for compliance with quality system policies and procedures.
• Release finished goods for distribution.
• Complete lot release documentation.
• Review records for completeness and verify that required documentation has been fulfilled.
• Collect and store retain samples.
• Tag approved product, as applicable.
• Maintain, archive, scan, and organize quality records.
• Assist with sample receipt and management of laboratory supplies and materials.
• Test finished-goods samples under general supervision.
• Review quality analysis results and report issues as required.
• Collect and compile data related to recurring product defects and quality issues.
• Review raw material inspection logs and identify consistent failures.
• Gather information regarding defective products and materials.
• Monitor internal and external complaints and compile data for reporting.
• Support process improvement, LEAN, and Six Sigma initiatives.
• Communicate with team members and management regarding quality-related issues or opportunities.
• Follow GMP, quality system, environmental, health, and safety procedures.
• Maintain accurate manual and electronic documentation.
• Utilize applicable quality and computer systems, including Compliance Wire and ADAPTIV, as needed.
• Use laboratory/test equipment such as gauges and microscopes, where applicable.
• Consistently meet training and work-performance requirements.
• Perform other duties as assigned.

Qualifications

• Associate degree in Science, Technology, or a related field.
• 0–2 years of work experience preferred, or an equivalent combination of education and experience in an FDA-regulated environment.
• Strong attention to detail and organizational skills.
• Ability to manage multiple tasks and priorities.
• Strong verbal and written communication skills.
• Strong interpersonal and teamwork skills.
• Demonstrated analytical and statistical problem-solving abilities.
• Intermediate or advanced computer and database management skills.
• Proficiency with standard office equipment, including copiers and scanners.
• Ability to learn and apply operating procedures and related computer systems.
• Ability to work effectively in a fast-paced, team-oriented environment.

Work Environment & Requirements

• Ability to work a Tuesday–Saturday schedule after completion of training.
• Overtime may be required based on business needs.
• Ability to work onsite in Cornelia, GA.
• Approximately 2 trips per month to Athens, GA.
• Ability to follow GMP, quality, safety, and environmental procedures.
• Safety glasses and other PPE may be required.
• Ability to perform computer entry and repetitive hand motions.
• Ability to sit, stand, and walk throughout the workday.
• Ability to lift/carry light to medium materials as required.

Why Apply?

This is an excellent opportunity for a science or technology professional looking to build experience in  quality control, GMP, batch review, product release, and regulated manufacturing within a global healthcare organization.

Apply today with Kelly Science & Clinical for immediate consideration.

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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. 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.

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