Technical Associate, Clinical Manufacturing - Andover, MA

Job Title

Take responsibility for individual contributions to achieve team deliverables, working effectively as a team member and coordinating with others.

Manage personal time and professional development, being accountable for results.

Follow standard procedures to complete tasks of varying scope, sequence, and complexity within the agreed timeframe.

Identify and solve moderately routine problems.

Complete assignments with moderate supervision using established procedures, referring deviations from standard procedures to the supervisor.

Ensure work is reviewed for accuracy, quality, and adherence to standards.

Engage in cross-functional communication with the tech transfer team, quality, and engineering as needed, and support continuous improvement initiatives using root cause analysis tools.

Implement Current Good Manufacturing Practices (part of GxP) and safe handling techniques for solid dosage processing within the continuous manufacture/PCMM work stream.

Perform Operator care tasks associated with the maintenance and operation of complex pharmaceutical manufacturing equipment.

Generate, assist, and execute documentation related to solid dosage manufacture, including working batch record documentation and in-process run sheets.