Job Title: Quality Control (QC) Engineer / Analyst
Location: Concord NC (Onsite)
Duration: Long Term Contract
Job Summary:
We are seeking a Quality Control (QC) professional to support laboratory testing and quality assurance activities within a GMP-regulated pharmaceutical manufacturing environment. This role will focus on analytical testing documentation and compliance ensuring products meet quality and regulatory standards.
The ideal candidate will have hands-on experience in QC testing data analysis and GMP documentation within pharma or biotech settings.
Key Responsibilities
Perform analytical testing on raw materials in-process samples and finished products
Document and review test results in compliance with GMP and regulatory requirements
Support method validation verification and transfer activities
Investigate out-of-specification (OOS) and out-of-trend (OOT) results
Maintain laboratory equipment and ensure proper calibration and qualification
Collaborate with Quality Assurance Manufacturing and Validation teams
Ensure compliance with FDA GMP and company quality standards
Support audit readiness and regulatory inspections
Required Qualifications
Bachelors degree in Chemistry Biology or related scientific field
2 6 years of experience in Quality Control within pharmaceutical or biotech industry
Hands-on experience with analytical techniques (e.g. HPLC GC UV etc.)
Strong understanding of GMP and regulatory compliance
Good documentation and data integrity practices
Job Title: Quality Control (QC) Engineer / Analyst Location: Concord NC (Onsite) Duration: Long Term Contract Job Summary: We are seeking a Quality Control (QC) professional to support laboratory testing and quality assurance activities within a GMP-regulated pharmaceutical manufacturing environm...
Job Title: Quality Control (QC) Engineer / Analyst
Location: Concord NC (Onsite)
Duration: Long Term Contract
Job Summary:
We are seeking a Quality Control (QC) professional to support laboratory testing and quality assurance activities within a GMP-regulated pharmaceutical manufacturing environment. This role will focus on analytical testing documentation and compliance ensuring products meet quality and regulatory standards.
The ideal candidate will have hands-on experience in QC testing data analysis and GMP documentation within pharma or biotech settings.
Key Responsibilities
Perform analytical testing on raw materials in-process samples and finished products
Document and review test results in compliance with GMP and regulatory requirements
Support method validation verification and transfer activities
Investigate out-of-specification (OOS) and out-of-trend (OOT) results
Maintain laboratory equipment and ensure proper calibration and qualification
Collaborate with Quality Assurance Manufacturing and Validation teams
Ensure compliance with FDA GMP and company quality standards
Support audit readiness and regulatory inspections
Required Qualifications
Bachelors degree in Chemistry Biology or related scientific field
2 6 years of experience in Quality Control within pharmaceutical or biotech industry
Hands-on experience with analytical techniques (e.g. HPLC GC UV etc.)
Strong understanding of GMP and regulatory compliance