Job Description

Employee Responsibilities:

Perform method development, feasibility, qualification and/or validation of methods in support of large molecule biopharmaceutical products

Document work as required for GMP compliance

Perform tests accurately

Troubleshoot method and instrumentation problems

Use office and instrumentation specific computer software

Produce documents (e.g., characterization reports, methods and client reports)

Develop and execute validation plans

Give presentations for training and client reviews

Train technical staff