Scientist I

Location: Athens, GA 30601 (75%) / Cornelia, GA 30531 (25%)

Pay: $28–$35/hour (based on experience)

Shift: Full-Time, Day Shift

Contract Length: 12+ Month Contract with potential for extension

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.

	
• 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, ComplianceWire, 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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