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PageGroup changes lives for people through creating opportunity to reach potential.
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Seeking a Regulatory Manager to join our team who will ensure compliance with all relevant regulations, standards and guidelines. This person will work closely with internal departments and provide guidence to ensure regulatory requirement are met.
The Sustaining Engineering Manager will be responsible for ensuring that all technical aspects of product design and manufacturing are managed with internal and external members and partners.
Lead the development of the Bioprocess Filtration Portfolio, leveraging both new and existing assets to meet market demands and industry trends. Serve as the subject matter expert on bioprocess filtration, providing technical support and guidance to internal teams and external stakeholders.
Responsible for driving our business development activities, expanding our client base, and providing strategic input to enhance our service offerings. Provide strategic input and innovative solutions to enhance our service offerings and differentiate us in the market.
Identify and pursue new business opportunities in the pharmaceutical and biotechnology sectors related to preclinical discovery and development. Leverage a strong technical background in preclinical research, with a focus on immuno-oncology, oncology, degenerative disorders, or related areas to effectively communicate with clients and internal teams.
The Senior Quality Engineer role involves planning and executing quality assurance tasks and testing for new product development, collaborating with cross-functional teams, and conducting risk assessments and statistical analysis. Responsibilities also include material selection, process validation, and participation in design verification and validation testing.
Collect operational risk data from departments. Review data input and follow up if needed. Consolidate data for risk aggregation and executive committee reporting. Analyze inputs and generate reports.
The Sustaining Engineering Manager will manage all manufacturing operations and product design as is pertains to the company's proprietary technology in the medical device space. You will manage multiple projects covering both R&D and sustaining work while communicating effectively with customers.
Lead the process development and production of ADCs. Support the development of the facility and laboratory design, build out, and start-up.
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