Quality Scientist/General Cell Biology

29 Jul 2022


  • Minimum B.S. in Biochemistry, Virology or related biological science is must.
  • Master's degree in Biochemistry, Virology or related biological science is plus.
  • Minimum 4 years of laboratory experience.
  • Demonstrated leadership and teamwork skills and ability to work independently.
  • Strong technical knowledge and high level of technical performance.
  • Laboratory experience, knowledge of laboratory operations and bioanalytical instrumentation.
  • Experience in virology and biochemistry techniques including ELISA, antibody production, and cell culturing, QPCR and cell line expansions.
  • Technical report writing experience is required.
  • Previous technical and/or analytical problem-solving experience in vaccine or biologics development, and/or quality site experience.
  • Proficiency in classical biochemistry or virology assays.
  • Experience in the following assays: ELISA, PCR, RNA Extractions, TCID50 assays, virus tittering, serum neutralization assays, plaque assays, cell culturing, Ouchterlony, cell banking.
  • GMP experience.
  • Statistical analysis experience with familiarity with JMP.
Project Description:
  • The Quality Scientist will be responsible for supporting Critical Reagent programs in a fast-paced environment within the Vaccine franchises.
  • The support is critical to testing within the Quality Control Laboratories.
  • The Quality Scientist is responsible for independently managing the complete lifecycle of Critical Reagents such as reference materials, positive controls, anti-sera, and other critical materials.
  • Release and stability testing of vaccine and biological products use these reagents.
  • Reagent lifecycle includes acquisition, certification and qualification testing, implementation and ongoing monitoring and replacement of the material as needed.
  • Additionally, the individual will work independently and demonstrate leadership in the implementation, execution, and management of reagents, as well as perform appropriate second person peer document reviews, support activities and project work associated with their position, and ensure work is conducted to the highest quality, compliant and conforms to current Good Manufacturing Practices and regulatory expectations.
  • Provide bioanalytical support to Global MMD sites as needed and respond to regulatory questions, author of analytical license sections.
  • 70% lab based/30% documentation.
This 24+ month position starts ASAP. Please E-MAIL your resume (attachment to email) with rate and availability to Maureen: ALPHA'S REQUIREMENT #22-02130 MUST BE ELIGIBLE TO WORK IN THE U.S. AS AN HOURLY W2 EMPLOYEE

  • ID: #44466323
  • State: Pennsylvania Westpoint 19486 Westpoint USA
  • City: Westpoint
  • Job type: Contract
  • Showed: 2022-07-29
  • Deadline: 2022-09-26
  • Category: Et cetera