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Job summary
An established industry player is seeking Bioequivalence experts to join their team in Chicago. This role involves providing consultation and remediation services across the pharmaceutical and biotechnology sectors. The ideal candidate will possess extensive experience in bioavailability, regulatory science, and project leadership. You will engage in innovative problem-solving and work closely with a talented team to ensure the successful development of high-quality medical products. If you are passionate about making a difference in the industry and have a proven track record in bioequivalence, this opportunity is perfect for you.
Qualifications
10 years of relevant experience in bioequivalence and biopharmaceutics.
Strong background in regulatory science and GCP/GLP audits.
Responsibilities
Lead bioequivalence studies and develop study protocols.
Conduct statistical analyses and ensure compliance with US FDA regulations.
Skills
Bioavailability expertise
Bioequivalence strategies
Biopharmaceutics
Regulatory science
GCP and GLP audits
Formulation development
Statistical data analyses
Project leadership
Communication skills
Problem-solving techniques
Education
B.S. in life sciences
Job description
An established industry player is seeking Bioequivalence experts to join their team in Chicago. This role involves providing consultation and remediation services across the pharmaceutical and biotechnology sectors. The ideal candidate will possess extensive experience in bioavailability, regulatory science, and project leadership. You will engage in innovative problem-solving and work closely with a talented team to ensure the successful development of high-quality medical products. If you are passionate about making a difference in the industry and have a proven track record in bioequivalence, this opportunity is perfect for you.