Analyst, Quality Control

Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
The Analyst, Quality Control will perform testing and sampling to support manufacturing, validation, process development and stability studies in a GMP environment.
Key Responsibilities:
Perform and review routine assays for HPLC, ELISA/cell-based immunoassays, and/or electrophoresis (SDS-PAGE/IEF) with strict adherence to written analytical test procedures.
Perform aseptic sampling, visual inspection, pH, conductivity, osmolality, and spectrophotometry.
Review, revise and write test methods, standard operating procedures. In addition to performing QC testing, the Analyst may support validation projects, investigations, and method development projects.
Other functions include but are not limited to writing study protocols and reports; training other analysts; working with other departments in developing, revising, and implementing QC procedures and policies.
Knowledgeable of company cGMPs as well as industry regulations that apply to all job functions.
Participate in regulatory inspections.
Support continuous improvement initiatives.
Other duties as assigned.
Minimum Qualifications:
Bachelor’s degree in biology, biochemistry, chemistry or equivalent scientific field or a minimum of 2 years of relevant, hands-on experience working in a QC or analytical lab or equivalent combination of education/experience.
Experience with analytical testing and equipment, writing reports/procedures/specifications, GMPs and regulatory audits are essential.
Must be proficient with ELISA, Analytical Biochemistry or chemistry.
Position Type/Expected Hours of Work:
This role is a full-time onsite position. Days and hours of work are Monday through Friday,