What are the responsibilities and job description for the Senior Analyst I, Quality Control Chemistry position at Tandym?
A recognized pharma company is hiring a Senior Analyst I, Quality Control Chemistry on a one-year contract basis near Boston, MA. **This position is for candidates who are able to work on a W2 basis.**Responsibilities: Execute analytical test methods to support product release and stability of AAV products using different analytical techniques (e.g. HPLC, LCMS, AUC, UV, CE-SDS, compendia methods like Osmolality, pH, Sub visible particulates and Appearance)Review and approval of cGMP analytical data for release and stability testing from chemistry analytical test methodsSupports and leads QC Chemistry laboratory operations (ex. Instrument qualification and maintenance. Housekeeping, qualify critical reagents, etc).Author and support quality events; Change controls, Deviation, CAPA, OOS Investigation, as neededWrite, prepare, and present technical data, technical reports, and standard operating procedures (SOPs), Method transfer/ validation protocol, Method transfer/ validation report for internal and external methodsPerform other duties, as neededQualifications:5 years of experience working in cGMP environmentBachelor's and/or Master's Degree in Analytical Chemistry, Biochemistry, Biophysics, or a related disciplineExperience working in the cGMP QC lab of the Pharmaceutical or Biopharmaceutical industry Experience working with external contract labs (CMOs, CROs)Desired Skills:Experience analyzing Nucleic Acids, Virus Capsids, Antibodies, and/or other Biologics materials using HPLC/UPLC, LCMS, AUC, UV- Vis, CE-SDS
Salary : $21 - $28