Job Title: Scientist II 
Company: Kelly Science & Clinical (on behalf of a leading medical device organization)
Location: Cornelia, GA (training may be in Athens, GA or vice versa)
Employment Type: 6 month contract, potential for extension
Pay: $30/hr-$35/hr
Shift: Monday-Friday, 8am-5pm

Position Summary

Kelly Science & Clinical is seeking a Scientist II to support biological testing and product development activities within a regulated laboratory environment. This role involves designing and executing biological experiments, performing routine and complex laboratory testing, and supporting manufacturing operations to ensure timely product delivery.

The Scientist II will work under general supervision, applying established scientific practices and techniques while ensuring compliance with cGMP standards and internal procedures.

Key Responsibilities

• Perform environmental monitoring, laboratory assays, and biomarker identification/development
  

• Conduct biological indicator, endotoxin, bioburden, growth promotion testing, and microbial identification
  

• Execute routine and complex testing to support manufacturing and product release timelines
  

• Perform raw material, in-process, and finished goods testing upon completion of training
  

• Analyze and interpret data; provide scientific input based on current literature
  

• Initiate and participate in investigations for non-conforming results
  

• Maintain accurate documentation in compliance with Good Documentation Practices (GDP)
  

• Troubleshoot methodologies and laboratory instrumentation
  

• Perform calibration, verification, and maintenance of lab equipment per SOPs
  

• Utilize laboratory software systems and prepare reagents, standards, and controls
  

• Support training activities and provide peer data review
  

• Ensure compliance with cGMP, safety, and environmental regulations

Qualifications

Education:

• Bachelor’s degree in a scientific discipline required
  

• Master’s degree preferred

Experience:

• Bachelor’s degree with 2–5 years of relevant laboratory experience, or
  

• Master’s degree with 0–3 years of experience
  

• Experience in a cGMP environment required
  

• Chromatography experience (GC and HPLC) required
  

• Experience with Empower Chromatography Software required
  

• Test method validation and analytical method development experience preferred

Required Skills & Competencies

• Strong understanding of quality systems and laboratory compliance
  

• Ability to work independently with minimal supervision
  

• Excellent organizational, communication, and interpersonal skills
  

• Strong attention to detail and problem-solving abilities
  

• Self-motivated with the ability to manage multiple priorities
  

• Ability to collaborate effectively with cross-functional teams

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