Independently perform GMP and non-GMP Quality Control testing of AAV and LNP mRNA samples
1–3 years of relevant biotechnology or pharmaceutical industry experience
Master's degree with 0–1 year of relevant experience
Document all testing activities and results accurately in compliance with internal and regulatory standards
Strong theoretical understanding of macromolecules (e.g., DNA, RNA, proteins) and their chemical properties
Bachelor's degree in Analytical Chemistry, Biochemistry, or a related discipline with 1–3 years of relevant biotechnology or pharmaceutical industry experience
Support analytical method development, qualification, and transfer for LC, CE, and MP assays
Previous experience working in a GMP environment with demonstrated ability to comply with all applicable GMP standards and documentation practices
Familiarity with regulatory requirements for genomic medicine development, including appropriate control and testing strategies

Quantitative Researcher

AAA Global

Boston, MA 02298

Research Associate - iPSC Platform Development

Stratacuity: Proven Scientific Placement

Cambridge, MA 02140

Swissport International AG

East Boston, MA 02128

Must be computer literate, and either possess or have the ability to learn Sabre and Microsoft applications such as PowerPoint, Excel, and Word.
Valid driver's license.
Must be able to work in inclement weather.
Ability to write clear, concise reports and correspondence.
High School Diploma and at least one-year certificate from a university, college or technical school, or six-months to one-year related experience; or equivalent combination of education and experience.
Ability to read and interpret documents such as safety, operational, and procedural manuals.
Ability to speak effectively before groups of people to include the airline customers, fueling company personnel, and the airport authority.
High School Diploma or equivalent.