Sr Associate
Target PR Range: 20-28/hr
*Depending on experience
• Participate in the planning, design, execution, and documentation of studies related to drug product formulation and process development in support of commercialization and life cycle management of biologics.
o Support and conduct related studies, e.g. UF/DF, filtration, freeze/thaw and fill/finish, for products in various formulations and formats (liquid, lyophilized, etc.).
o Evaluate process and product performance through analytical testing via measurement of pH, conductivity, osmolality, protein concentration, HPLC and CE methodologies, solid state characterization, particle quantitation/characterization, physical properties, etc.
• Data analysis and documentation/review in electronic notebooks.
• Author, review, and data verify technical documents such as protocols, reports, regulatory documents, etc.
• Clearly and consistently communicate data in progress reports and presentations.
• Participate in cross-functional teams in a fast-paced environment to progress product development.
• Adhere to all training, compliance, and safety guidance.
• Support lab operations and inspections as required of all lab-based staff.
• Work primarily onsite with remote work as appropriate to role and tasks.
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