Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The responsibilities for the position include: QC assays, testing, documentation, QC analysis, and validation.Responsibilities:- QC Assays (ELISA Assays, HPLC Analysis of Plasmid iso-forms, Wet Chemistry Techniques)- Testing- Documentation (write protocols for test method validation and Qualifications, write development reports, validation, and other relevant technical reports)- QC Analysis (HPLC software)- Validation (Qualification of USP/compendia methods, Tech transfer of assays, Test Method validation, Qualification of new equipment)Working hours: 12:00 AM - 12:00 PM (Various Shifts Available)Skills:- Assay development experience- Experience with gPCR is a must- Method development and optimization experience in a cGMP environment a plus- Experience with chromatography, gel electrophoresis, and microbiology techniques are preferredEducation:BachelorsExperience:1-4 yearsQualifications:Candidates should have a Bachelor???s or Associate's degree and 3+ years of relevant experience and 2-5 years of assay development experience Apply today at 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.