Provide technical support for Validation activities as needed to complete Equipment PQs in accordance with the annual schedule.
Execute annual PQs of critical process equipment in accordance with approved validation protocols.
Perform validation activities as needed that may require flexibility in their schedule to minimize operational impact and support timely completion.
Develop understanding of new process equipment and procedures relative to validation requirements.
Support recommendations and implementations of corrective and preventative actions to reduce atypical events and or validation deviations.
Qualifications:
Bachelor’s degree in, Biology, Biochemistry, Biochemical Engineering, Biological Systems Engineering, Biomedical Engineering, Chemical Engineering, or Integrated Science with minimum two years of experience in Vaccine Manufacturing.
Associate degree in, Biology, Biochemistry, Biochemical Engineering, Biological Systems Engineering, Biomedical Engineering, Chemical Engineering, or Integrated Science with minimum four years of experience in Vaccine Manufacturing.