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Quality Control Chemist - I

Quality Control Chemist - I

Integrated Resources, IncFrederick, MD, US
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Job Description

Job Description

Job Title : Quality Control Chemist - I

Location Available : Frederick, MD 21704

Duration : 4 Month+ Contract (Possibilities of Extension)

Pay Range : $26 - $28.80 / hr. on W2

Shift :

  • Wed–Saturday (Day or Swing shift, flexible)
  • Important : All contractors are required to work Mon–Fri (7 : 30 AM–4 : 00 PM) for the first 7 weeks to complete onboarding and technical training.
  • Post-training, the agreed-upon shift will begin.

Position Overview :

We are seeking a Quality Control Chemist to support analytical testing for raw materials, in-process materials, and final products in a cGMP-compliant environment. This role is essential to ensuring the integrity and quality of biopharmaceutical products by performing a range of assays and supporting lab functions.

Key Responsibilities :

  • Perform routine testing using methods such as :
  • Cell-based bioassays

  • Flow Cytometry
  • ELISA
  • qPCR
  • Maintain lab operations, including calibration and routine maintenance of instruments
  • Support data review , trending, and document verification to aid in CoA (Certificate of Analysis) generation
  • Author or revise Standard Operating Procedures (SOPs) , qualification, and validation documents
  • Contribute to and support lab investigations , including OOS (Out of Specification) root cause analyses
  • Ensure compliance with GMP standards and internal policies
  • Participate in continuous improvement initiatives by gathering and analyzing QC metrics
  • Represent QC in daily / weekly meetings and communicate testing progress and issues
  • Basic Qualifications :

    Candidate must meet one of the following criteria :

  • Bachelor’s degree in a scientific discipline
  • Associate’s degree and 2+ years of QC or biotech industry experience
  • High school diploma and 3+ years of QC or biotech industry experience
  • Preferred Qualifications :

  • Experience in GMP-compliant environments and knowledge of 21 CFR Part 11 / 210 / 211 regulations
  • Strong understanding of QC workflows , lab instrumentation , and data integrity principles
  • Hands-on experience with :
  • Flow Cytometry

  • ELISA
  • PCR
  • Cell-based assays
  • Familiarity with OOS investigations , deviations, and quality documentation
  • Proficiency in MS Office Suite (Excel, Word, PowerPoint)
  • Excellent written and verbal communication skills
  • Self-driven with the ability to work independently or within cross-functional teams
  • Experience in biotech and / or pharmaceutical industry strongly preferred.
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    Quality Control Chemist • Frederick, MD, US