QC Raw Materials Lead

? Mahwah, NJ
? $41,000 – $48,000 per year
? Full-Time | Exempt
? Kelly Science & Clinical

Kelly Science & Clinical is seeking a QC Raw Materials Lead to support quality control operations at a growing manufacturing and laboratory facility in Mahwah, NJ. This role will focus on testing and releasing raw materials, coordinating testing activities, and ensuring compliance with GMP and laboratory quality standards.

This is a great opportunity for a recent graduate or early-career scientist with a background in chemistry, biology, or a related field who is looking to grow their career in quality control and laboratory operations.

Key Responsibilities

• Perform raw material testing, including physical attribute evaluation and FTIR identification testing

  
  

• Execute additional analytical tests such as moisture content, viscosity, and pH as directed by the Quality Manager

  
  

• Coordinate raw material testing activities across internal and external departments

  
  

• Maintain ownership of the internal system used to release raw materials

  
  

• Review Certificates of Analysis (CoA) and coordinate required testing

  
  

• Document all testing activities in accordance with GMP and SOP requirements

  
  

• Initiate and draft Supplier Corrective Actions for raw material suppliers when needed

  
  

• Perform sampling of incoming raw material containers

  
  

• Manage retain samples and sample storage

  
  

• Prepare samples for microbiological and assay testing

  
  

• Investigate and report noncompliant materials

  
  

• Assist with inventory management and instrument calibrations

  
  

• Support additional quality or laboratory tasks as assigned

Qualifications

• Bachelor’s degree in Chemistry, Biology, or a related scientific field

  
  

• 0–2 years of laboratory or quality control experience

  
  

• Understanding of GMP, GLP, and Good Documentation Practices

  
  

• Strong attention to detail and organizational skills

  
  

• Ability to manage multiple tasks and work collaboratively in a team environment

  
  

• Strong written and verbal communication skills

  
  

• Proficiency with Microsoft Office Suite

What You’ll Bring

• Strong laboratory and documentation practices

  
  

• Ability to work in a GMP-regulated environment

  
  

• Detail-oriented mindset with strong problem-solving abilities

  
  

• Collaborative approach to working with cross-functional teams

? Apply today to learn more about this opportunity with Kelly Science & Clinical.

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