Quality Release Technician

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

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.

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.

• 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.

• 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.

• 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.

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.