Supports the PU in all process-specific issues, drives continuous process improvement for quality and quantity and ensures GMP requirements are met and guidelines and SOPs are followed. Provide continuous supply of high quality products that meet...

Summary: This senior position is responsible for providing quality oversight to ensure GMP equipment, process, systems, and facility/utilities are qualified and maintained in a validated state. Performs the QA review and approval of equipment and...

Fantastic opportunity to lead the Commissioning and Qualifications activities for a state of the art GMP Biologics facility. Come join an experienced and highly respected Engineering leadership team at a top biopharmaceuticals company in the Boston...

Summary: QA Specialist is responsible for implementing, managing, and directing the Quality Assurance Program for a Laboratory that provides bioanalytical services including sample management, method development, method validation, and clinical...

ENGINEER: Assistant or Associate Level # 2013-04 JOB SUMMARY: ACEA Biosciences, Inc. is looking for an Assistant/Associate Engineer with the following abilities, (under limited supervision from research scientists and engineers) building,...

ADVENT Consulting Canada Inc., is an engineering consulting firm serving the pharmaceutical and biotechnology industries. Head-quartered in San Francisco, California, and with operations in the Eastern US (NC), and Asia-Pacific, our company is...

Job Purpose The Validation Specialist is to ensure systems and operations are compliant with regulatory and Novartis requirements through preparation of risk assessments, preparation and execution of validation protocols and final reports. There will...

In this role you will be responsible for review and closure of inquiries and complaints and for supporting the CAPA system. Review and analyze data and manage documentation as it pertains to the complaint and CAPA programs. Will track, trend, and...

In this role you will be responsible for review and closure of inquiries and complaints and for supporting the CAPA system. Review and analyze data and manage documentation as it pertains to the complaint and CAPA programs. Will track, trend, and...

Supports day to day site compliance needs on the shop floor. Identifies and resolves compliance issues within the Process Unit unilaterally and cross-functionally. Works closely with the Process Units and Quality Organization to ensure compliance...