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The Equipment Lead, Form Fill coordinates equipment operations in a cleanroom environment, overseeing the filling lines. Responsibilities include troubleshooting equipment issues, assisting manufacturing personnel, and ensuring compliance with safety and quality standards.

The Associate Scientist, QC is responsible for conducting release and identification testing of raw materials, operating Quality Control equipment, documenting test results, and maintaining laboratory standards. This includes data entry into LIMS, writing SOPs and reports, and ensuring compliance with cGMP regulations in a laboratory setting.

The Operator III, Formulation is responsible for measuring and formulating drug products according to batch records. Key tasks include aliquoting liquids and powders, performing sterile filtration, conducting integrity testing of product filters, and cleaning tanks with automated equipment.

The Sr. Compliance Specialist will manage and facilitate regulatory inspections and internal audits, ensuring compliance with quality standards and regulatory requirements. Responsibilities include oversight of audit responses, training, and collaboration with site experts to maintain adherence to Good Manufacturing Practices and related regulations.

The Associate Project Manager oversees multiple projects in the pharmaceutical sector, focusing on inventory tracking, billing, and project execution. Responsibilities include generating reports from the ERP system, managing project deliverables, facilitating customer meetings, and ensuring timelines are met. They assist the Project Management team in achieving project goals and maintain communication with stakeholders.

The QA/RA Compliance Specialist ensures compliance with pharmaceutical regulations by managing change controls, preparing regulatory filings, and collaborating with various departments. Responsibilities include assisting in SOP development, supporting audits, and liaising with customers.

The Associate Scientist engages in pharmaceutical development and clinical manufacturing projects, overseeing tasks like formulation, data interpretation, and documentation while ensuring timely execution of responsibilities and ongoing communication with internal teams and clients.