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Join Precision for Medicine, a leader in advanced therapy technical operations consulting, as a Project Engineer. Responsibilities include providing hands-on support for engineering life cycles, authoring technical documents, executing validation protocols, and building relationships with clients. Bachelor's degree in Life Science or Engineering required. Full-time on-site presence and willingness to travel up to 100% needed. COVID vaccine mandatory. Competitive salary and benefits offered.
Join Precision for Medicine, Manufacturing Solutions as a Sr. Project Engineer I. Responsibilities include creating alignment with client departments, providing hands-on support for engineering life cycles, authoring technical documents, and executing validation protocols. Requires a Bachelor's degree in Life Science or Engineering and a minimum of 1 year of relevant experience.
The Senior Project Controls Engineer will create alignment with various departments, provide hands-on support for manufacturing processes, produce project controls deliverables like budgets and schedules, identify roadblocks, and build relationships with clients. The role involves a commitment to the company’s mission and potential travel requirements.
Project Farma is a leading consulting firm in advanced therapy technical operations, focusing on biomanufacturing and project management for gene and cell therapy and biotech companies. They aim to advance operational excellence and speed to market for innovative treatments, while fostering a culture of teamwork and professional development.
The Project Controls Engineer will support cross-functional teams, providing project management and engineering lifecycle assistance. Responsibilities include managing project budgets, schedules, risk assessments, and producing detailed project reports to enhance operational excellence in life sciences.
As a Project Engineer, you will collaborate with clients in the life sciences sector, providing engineering support and troubleshooting for advanced manufacturing processes. You are responsible for authoring technical documents, executing validation protocols, and fostering cross-functional alignment to ensure project success while embodying a patient-focused mission.
The Project Engineer will create alignment with client departments, provide support for engineering processes, author technical documents, execute validation protocols, and build relationships while contributing to a patient-focused mission.
This position involves conducting various immunological assays, maintaining cell cultures, performing QC analyses, and supporting new product development. Responsibilities include documentation, training staff, and ensuring lab safety and compliance with SOPs.
As a CQV Engineering Consultant, you will coordinate with clients to support engineering processes in the life science industry, lead project initiatives, develop technical documentation, mentor team members, and contribute to business development efforts.
The Cellular Assay Scientist is responsible for developing, validating, and performing clinical assays in an accredited laboratory, specifically focusing on neutralizing antibody assays. This role entails designing experiments, analyzing data, improving lab procedures, and ensuring compliance with safety standards. Collaboration with technical teams and supporting equipment qualifications are also key responsibilities.
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