Main Purpose of Role
- Evaluate changes in onmarket product design and manufacturing process through independent experimental design, analytical testing, data analysis
- Assist in process development, characterization, and validation in molecular reagent manufacturing
- Author and/or execute approved protocols, reports and other records
Skills preferred
- Understanding of GDP and GMP
- Understanding of 21 CFR Part 820 regulations and equivalent
- Experience in assay design and Design of Experiment
- Statistical experience, JMP or Minitab preferred
- Manufacturing Process Development and/or Validation Experience
- Understanding of qPCR theory, methods and analysis
Qualifications preferred
- Ph.D in Biochemistry, Molecular Biology, Chemistry, Chemical Engineering or related discipline with 03+ years of experience
- Masters in Biochemistry, Molecular Biology, Chemistry, Chemical Engineering or related discipline with 25+ years of experience
Minimum qualifications required
- B.S./B.A. in Biochemistry, Molecular Biology, Chemistry, Chemical Engineering or related discipline with 5+ years of experience
Job Type: Contract
Salary: $35.00 - $40.00 per hour
Expected hours: 40 per week
Benefits:
- Paid time off
Schedule:
- 8 hour shift
Education:
- Bachelor's (Required)
Experience:
- Molecular biology: 3 years (Required)
- Design of Experiment: 3 years (Required)
- Assay Design: 3 years (Required)
- Minitab: 3 years (Required)
- qPCR theory: 3 years (Required)
Work Location: On the road