The primary purpose of this position is to ensure quality assurance and compliance activities. This person will be responsible for production, testing, and associated documentation is within industry guidelines.Responsibilities:*Assemble applicable documentation *Process CAPAs and perform routine internal audits and maintain quality control.*Maintaining supplier files and audits*Proper documentation of equipment *Training new employees*Develop quality system SOPs*Inventory Products *Follow (GMPs) and (SOPs)*Review and approve Analysis Certificates*Print and approve product labelsWorking hours: 8:00 AM - 5:00 PMSkills:*Plasmid purification and microbiology techniques *Quality Assurance documentationEducation:BachelorsExperience:4-7 yearsQualifications:*GMP experience*Bachelors degree in applicable life science field www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.