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The MRO Buyer coordinates indirect purchasing for ancillary operations, assists with purchase orders and vendor management, manages budgets and invoices, supports continuous improvement activities, and acts as a subject matter expert for procurement processes.

The Specialist, QA OTF provides Quality Assurance oversight for GMP Manufacturing, focusing on operations for biological products. This role includes on-floor QA activities, documentation review, compliance monitoring, and continuous improvement initiatives while collaborating with manufacturing teams.

The Quality Systems Specialist (Training) manages training documentation and LMS, develops training curriculums, supports audit preparations, reports training metrics, and conducts training sessions. This role ensures compliance with regulatory requirements and promotes effective training practices across departments.

The Quality Control Analyst I conducts QC testing and analytical activities, executing chemical and physical analyses of materials, compiling data for documentation, and participating in investigations and report preparations in compliance with regulations.

The Supervisor, QC will oversee environmental monitoring activities ensuring quality standards are met in drug manufacturing. Responsibilities include executing work, coordinating with stakeholders, maintaining processes, and managing environmental monitoring data trends.

The Specialist III, Form/Fill role provides technical support to manufacturing operations focusing on documentation, equipment, testing, and training. The position involves proposing process improvements, troubleshooting machine setups, collaborating with other staff to resolve issues, and ensuring operational efficiency in a cleanroom environment.

The Senior Representative, QA will manage facility audits, support the quality systems team, participate in internal audits, review audit findings responses, and enhance quality system effectiveness while collaborating with cross-functional teams on process improvements.