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
- Good documentation and data integrity practices
View more
View less