More jobs:
Scientist, Quality Control - QC Analysts/Managers
Job in
Cornelia, Habersham County, Georgia, 30531, USA
Listed on 2026-07-16
Listing for:
Kelly
Full Time
position Listed on 2026-07-16
Job specializations:
-
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers
Job Description & How to Apply Below
Location: Cornelia
Scientist I – GMP Laboratory Operations
Location:
Cornelia, GA Pay: $24–$25/hour (based on experience) Shift: Full-Time, Day Shift
We are seeking a motivated and detail-oriented Scientist I to support laboratory operations within a regulated manufacturing environment for a leading global medical device organization. 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
- 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
- Experience in medical device, pharmaceutical, or regulated manufacturing industries
- Familiarity with laboratory data systems and electronic documentation
- Exposure to LEAN or Six Sigma methodologies
This is an excellent opportunity to join a highly respected organization supporting innovative healthcare products in a collaborative laboratory environment.
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