Quality Control Analyst I
Durham County, NC - USA
Job Summary
Quality Control Analyst I Job Summary
Location: Research Triangle Park NC 27709
Duration: 12 months (Contract)
Bill Rate: $45.72/hr
Role Impact & Expectations:
As a Quality Control Analyst I you will play a key role in supporting the release and advancement of innovative gene therapy programs. Your focus will be on analytical testing of rAAV vector lots directly contributing to the company s capsid technology development and early-stage gene therapy pipeline. The position requires hands-on expertise in molecular biology and biochemistry methods strict adherence to protocols and effective data management.
Emphasis on Skills:
Candidates with strong molecular biology and biochemistry technical skills such as qPCR d/ddPCR ELISA HPLC endotoxin testing will thrive in this environment. Attention to detail with SOPs and data analysis is critical.
Key Responsibilities:
- Execute routine and complex molecular biology and biochemistry assays (qPCR d/ddPCR ELISA HPLC endotoxin)
- Analyze and review data following completion of test methods
- Assist with evaluation of analytical results and preparation of final reports
- Document procedures and results according to SOPs and quality standards
- Contribute to updates of work instructions SOPs forms and electronic laboratory records
- Participate in technical discussions and investigations
- Support management of lab materials supplies and sample inventory
- Maintain clean and organized laboratory spaces and ensure equipment readiness
Recruiter Insights:
- Attractive contract role in a high-profile biotech hub (Research Triangle Park)
- Work at the forefront of gene therapy technology
- Immediate impact on critical research and development projects
- Competitive bill rate
- Opportunity for candidates with limited (0 2 years) experience
- Preferred: Experience with electronic laboratory notebooks and rAAV/gene therapy analytics
Candidate Insights:
- Gain hands-on experience with advanced molecular and biochemical techniques
- Contribute to cutting-edge gene therapy programs in a collaborative R&D environment
- Work in a state-of-the-art facility with exposure to novel technology platforms
- Build foundational expertise for a career in analytical and quality sciences
- Preferred skills offer growth opportunities but are not required
Location: Research Triangle Park NC 27709
Duration: 12 months (Contract)
Bill Rate: $45.72/hr
Role Impact & Expectations:
As a Quality Control Analyst I you will play a key role in supporting the release and advancement of innovative gene therapy programs. Your focus will be on analytical testing of rAAV vector lots directly contributing to the company s capsid technology development and early-stage gene therapy pipeline. The position requires hands-on expertise in molecular biology and biochemistry methods strict adherence to protocols and effective data management.
Emphasis on Skills:
Candidates with strong molecular biology and biochemistry technical skills such as qPCR d/ddPCR ELISA HPLC endotoxin testing will thrive in this environment. Attention to detail with SOPs and data analysis is critical.
Key Responsibilities:
- Execute routine and complex molecular biology and biochemistry assays (qPCR d/ddPCR ELISA HPLC endotoxin)
- Analyze and review data following completion of test methods
- Assist with evaluation of analytical results and preparation of final reports
- Document procedures and results according to SOPs and quality standards
- Contribute to updates of work instructions SOPs forms and electronic laboratory records
- Participate in technical discussions and investigations
- Support management of lab materials supplies and sample inventory
- Maintain clean and organized laboratory spaces and ensure equipment readiness
Recruiter Insights:
- Attractive contract role in a high-profile biotech hub (Research Triangle Park)
- Work at the forefront of gene therapy technology
- Immediate impact on critical research and development projects
- Competitive bill rate
- Opportunity for candidates with limited (0 2 years) experience
- Preferred: Experience with electronic laboratory notebooks and rAAV/gene therapy analytics
Candidate Insights:
- Gain hands-on experience with advanced molecular and biochemical techniques
- Contribute to cutting-edge gene therapy programs in a collaborative R&D environment
- Work in a state-of-the-art facility with exposure to novel technology platforms
- Build foundational expertise for a career in analytical and quality sciences
- Preferred skills offer growth opportunities but are not required