Christina Johansson Email & Phone Number

Concord, California, United States

• Primary contact for domestic and international suppliers, directing production output, business development, and capacity expansion planning/implementations• Technical guidance and problem-solving proficiency, combined with strong interpersonal skills, to achieve well-balanced collaborative results• Manage meetings and business reviews to monitior supplier activities and maintain timelines• Provide updates, schedules, and cost analyses to core teams and management• Interact with Quality, Finance, Operations, Legal, and Planning colleagues to ensure achievement of company targets

Concord, California, United States

• Primary contact for domestic and international suppliers, managing production output, quality concerns, and capacity expansion planning/implementations• Provide technical guidance and problem-solving proficiency, combined with strong interpersonal skills, to achieve well-balanced collaborative results• Manage meetings and business reviews to track supplier activities and maintain timelines• Provide updates, schedules, and cost analyses to core teams and management• Interact with Quality, Finance, Operations, Legal, and Planning colleagues to ensure achievement of company targets• Routine domestic and international travel to ensure supplier performance

San Francisco Bay Area

Hands-on consultant working with medical device companies. Managed comprehensive validation efforts for large-scale technology and site transfers:• Implementation of 114K ft2 LA medical device manufacturing campus, including qualification of critical utility systems and multi-level walk-in cold boxes• Successful relocation and qualification of transplant diagnostic technology lines contributed to $17M in annual product revenue• Successful relocation and qualification of medical devices diagnostic and particle technology lines contributed to $30M in annual product revenue• Implemented 87K ft2 SF Bay Area medical devices facility • Managed transplant diagnostic technology product line relocation - Validation Master Plan and risk assessment creation and maintenance, resource management, validation protocol/report generationManaged critical manufacturing supplier activities in support of medical device regulatory filings and routine commercialization:• Coordinated activities supporting key supplier manufacturing operations and process changes• Managed supplier activities and maintained timelines• Provided updates, schedules, and cost analyses to core team and management• Audited supplier sites during development and manufacturing operations• Reviewed supplier manufacturing and validation documentationManaged key corporate initiatives and validation projects:• Managed site-wide transition of high-throughput analytical test platforms for manufacturing and testing operations, including qualification of new analyzers and transition of exiting products to new platforms• Implemented and qualified new critical raw materials and packaging parts• Generated company-wide gap assessment in response to critical customer audit findings - Emphasis on identifying corrective actions to improve product quality and reliability, thereby ensuring customer satisfaction and an ongoing supply of safe and effective products

San Francisco Bay Area

• Primary scientist for development of plasma pathogen inactivation product, working with key external manufacturing suppliers and test sites• Concurrently managed staff of 3 engineers leading independent development projects

San Francisco Bay Area

• Led department with primary technical responsibility for management of critical raw material suppliers and company validation activities• Successfully managed international technology transfer of critical raw materials to new supplier upon company divestiture• Managed staff of 2 engineers. Reported to VP of Quality Affairs

San Francisco Bay Area

Process Engineering Scientist -1992-1996• Managed technical aspects of critical raw material (recombinant protein and substrate) suppliers• Responsible for raw material and production technical support, issue resolution, and scale-up initiatives• Engineering lead in key site relocation validation and acquisition initiativesManufacturing Development Chemist (New Product Transfer) - 1990-1992 • Responsible for implementation, transfer, training, and ongoing support of new diagnostic immunoassay products from R&D to Production