Scientist I Job Cornelia Georgia USA,Quality Assurance

Location: Cornelia

Scientist I

Location:

Cornelia, GA Pay: $24–$25/hour (based on experience) Shift: Full-Time, Day Shift Kelly Science is currently seeking a Scientist I for a long-term engagement at one of our Global medical device clients in Cornelia GA. If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.

The role is eligible for medical benefits, paid time off including vacation (PTO), and holidays, 401K, and annual performance reviews. This role is responsible for routine analytical testing, documentation, equipment verification, and compliance activities to support manufacturing operations and timely product release.

Key Responsibilities

Prepare testing materials and laboratory samples
Perform and monitor routine analytical testing using laboratory instrumentation including:

HPLC
GC
FTIR
Instron
Viscotek
Glass viscosity meters

Operate measurement and inspection equipment such as microscopes, Starrett gauges, and Mitutoyo gauges
Document testing results and maintain accurate laboratory records
Recognize and document issues or deviations during analysis
Initiate investigations related to non-conforming materials or laboratory results
Perform calibration and verification checks on laboratory instruments
Collect, organize, and prepare data for evaluation and reporting
Archive completed testing documentation
Maintain laboratory cleanliness and support environmental health & safety initiatives
Follow GMP, ISO, quality system, and safety procedures
Utilize systems such as SAP, LIMS, Compliance Wire, Maximo, and ADAPTIV
Support LEAN, Six Sigma, 6S, and Maintenance Excellence initiatives
Work collaboratively in a team-oriented environment

Qualifications

Bachelor's degree in Biology, Chemistry, Biochemistry, or related scientific field required
Minimum 2+ years of experience in a GMP laboratory environment
Experience performing analytical or polymer/monomer testing preferred
Knowledge of GMP and ISO requirements
Strong written and verbal communication skills
Excellent organizational and documentation abilities
Self-motivated with strong attention to detail

Preferred Experience

Experience in medical device, pharmaceutical, or regulated manufacturing industries
Familiarity with laboratory data systems and electronic documentation
Exposure to LEAN or Six Sigma methodologies