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Oversees Drug Substance and Drug Product Fill/Finish services, managing client relations, project timelines, team leadership, and financial aspects while ensuring project quality and compliance.

Manage the cGMP document lifecycle: review, control, issue, distribute, image, archive, and retrieve paper and electronic records (EtQ/EDMS). Ensure documentation accuracy, compliance with cGMP and SOPs, support audits and inspections, and coordinate with QA, technical teams, and clients.

The Principal Automation Engineer ensures automation systems compliance, leads project execution, and manages resources for multiple projects in cGMP environments.

The Senior Research Associate executes experimental protocols in analytical laboratories, performs bio-analytical testing, conducts data analysis, and ensures compliance with safety and labeling procedures.

The role involves performing data reviews for biopharmaceutical analytical projects, ensuring compliance with cGMP standards, and providing feedback on analytical processes.

The ELN Administrator will support the ELN system, train users, perform data analysis, and ensure compliance with FDA regulations while leading system improvements.

Support downstream process development activities through experiment execution, data analysis, and technical documentation, while assisting in technology evaluation and equipment maintenance.

As a Senior Research Associate, you will conduct bio-analytical testing, data analysis, and maintain compliance with safety procedures, contributing to analytical programs in a dynamic environment.

The Executive Administrative Assistant I provides high-level administrative support to executives, manages calendars, coordinates meetings, arranges travel, and oversees expense reporting while ensuring effective communication across departments.

The Financial Analyst conducts complex financial analyses and reconciles data sets, ensuring data integrity for decision-making across departments.