Emily Swanson Email & Phone Number

Minneapolis, Mn, Us

Minneapolis, Mn, Us

St. Paul, Mn, Us

St. Paul, Mn, Us

Mumbai, Maharashtra, In

21201, Md, Us

• Expanded upon responsibilities held in the Lab Supervisor position to include coordinating projects and providing training, particularly related to quality and GLP, for all Principal Investigators in the Division of Translational Radiation Sciences (DTRS) and their staff• Continue to manage research projects conducted within the Division for both government and private sponsors• Drive for expansion and improvement of the GLP program and regulatory compliance• Supervise research staff and daily laboratory operations

21201, Md, Us

• Established FDA Good Laboratory Practice (21 CFR, part 58) compliant drug screening and model development capabilities in an academic environment making the division competitive for federal IDIQ and private industry contracts• Responsibilities while creating the GLP program included: Standard Operating Procedure (SOP) and data capture form development, staff training to encourage culture of quality, implementation of equipment management and qualification/validation policies, and quality system establishment for quality control review of data, risk assessment, deviation tracking and investigation, and research staff performance metrics• Successfully managed over 18.3 million dollars of government and corporate sponsored research projects requiring coordinated execution of multiple concurrent studies; respected budgets, evaluated and organized all raw data produced into informative deliverables that met study objectives• Managed laboratory staff and daily operations with emphasis on quality execution of research projects• Drove improvement of laboratory performance through incident analysis, anticipating potential risk areas, and evaluating completed studies and research staff utilizing metrics• Leveraged technical staff expertise to develop new and update existing Standard Operating Procedures and supporting documentation to meet evolving requirements of the laboratory• Contributed to study design from compliance and logistical perspectives; effectively communicated laboratory plans to staff, sponsors, subcontractors, and the Institutional Animal Care and Use Committee (IACUC)• Participated in both internal and external inspections of laboratory facilities and operations

21201, Md, Us

Hired by the Division of Translational Radiation Sciences based on years of experience in an FDA Good Laboratory Practice and ISO 17025 compliant environment to drive the establishment of a regulatory compliant pre-clinical drug and model development research facility.

Marlborough, Ma, Us

Filled the role of team lead within the testing laboratory by providing guidance, training, organization, and encouraging teamwork while continuing medical device testing and QC result reviewing responsibilities. Additionally responsible for investigating laboratory deviations to determine root cause, develop corrective actions, and drive improvement through policy or procedure changes. Authored validation and operation documents for new lab equipment.

Marlborough, Ma, Us

Responsible for performing environmental monitoring in medical device production and R&D facilities, conducting batch release testing on medical devices for the microbiology department, providing training to fellow lab technicians, and conducting Quality Control reviews of result reports.