Manufacturing Excellence, Regulatory Confidence.
Spokane, WA
Jubilant HollisterStier (JHS) CMO provides comprehensive sterile fill-finish and lyophilization services, ensuring the consistent delivery of high-quality products that meet the needs of global healthcare markets and patients worldwide. With decades of experience, we offer a flexible and collaborative partnership model for manufacturing excellence that enables our clients to increase speed to market with full regulatory confidence.
On-site · Kirkland
Provide technical support for pharmaceutical process engineering and technical transfer under senior guidance. Support the design, optimization, and implementation of aseptic manufacturing processes and documentation.
On-site · Kirkland
Lead the strategy, governance, and continuous improvement of the site's GMP training program to ensure regulatory compliance and workforce capability. Oversee LMS administration, personnel qualification programs, and inspection readiness to support operational excellence.
On-site · Kirkland
Oversee the operation and maintenance of building utility systems, including HVAC, boilers, and refrigeration, while ensuring regulatory compliance. Lead maintenance personnel, manage external contractors, and coordinate building-related projects and emergency responses.
On-site · Kirkland
Provide strategic and operational leadership for Quality Assurance activities supporting manufacturing and aseptic operations. Oversee batch disposition, deviation investigations, and CAPA management while ensuring continuous inspection readiness.
On-site · Kirkland
Provide real-time quality oversight of manufacturing and packaging operations to ensure strict compliance with GMP and regulatory standards. Review batch documentation, support quality investigations, and implement corrective and preventive actions (CAPA).
On-site · Kirkland
The role is responsible for managing deviations, conducting root cause analyses, and implementing corrective and preventive actions (CAPA) to ensure GMP compliance. It involves coordinating investigations across manufacturing and quality functions to ensure they are scientifically sound and inspection-ready.
On-site · Kirkland
Manage sterile production processes, daily schedules, and personnel to ensure efficiency and adherence to aseptic conduct principles. Oversee quality operations, including SOP updates and incident reporting, while supporting continuous improvement and new product implementation.
On-site · Kirkland
The Specialist, Compliance supports the Quality Systems & Compliance function by monitoring and strengthening site adherence to GMP and regulatory requirements. Key duties include managing audit readiness, tracking regulatory CAPAs, and overseeing supplier quality and regulatory surveillance.
On-site · Kirkland
Develop and execute qualification protocols for equipment, computerized systems, and manufacturing operations. Provide technical support for sterilization processes and ensure compliance with corporate standards and cGMP regulations.
On-site · Kirkland
Lead the governance and continuous improvement of the site's Quality Management System to ensure sustained GMP compliance and inspection readiness. Oversee critical quality processes including change control, CAPA governance, and supplier quality management while managing a team of quality professionals.
On-site · Kirkland
Responsible for the design, installation, and qualification of pharmaceutical equipment and systems for a facility expansion project. This includes managing vendors, overseeing budgets, and ensuring compliance with quality and safety guidelines.
On-site · Kirkland
Provide real-time quality oversight of pharmaceutical manufacturing and packaging operations to ensure GMP compliance. Review batch documentation, support quality investigations, and manage corrective and preventive actions (CAPA).
On-site · Kirkland
Manage the daily schedule of sterile manufacturing while ensuring strict adherence to aseptic conduct and quality standards. Lead and motivate the production team, oversee equipment maintenance, and manage KPIs to optimize operational efficiency.
On-site · Montréal
Oversee preventive, corrective, and predictive maintenance programs while ensuring compliance with internal and regulatory GMP standards. Manage CMMS data, lead quality investigations, and support the integration of new equipment and technical documentation.
On-site · Montréal
The Specialist supports the Quality Risk Management program by identifying, assessing, and mitigating quality and compliance risks. This includes conducting risk assessments like FMEA and maintaining documentation to ensure alignment with GMP and ICH Q9 standards.
On-site · Kirkland
Manage the daily schedule of sterile manufacturing while ensuring strict adherence to aseptic conduct and quality standards. Lead and motivate the production team, oversee equipment maintenance, and manage KPIs to optimize operational efficiency.
