Aeromechanical Engineer III - Lawrence

Fusion Life Sciences busca un Ingeniero III con experiencia en dispositivos médicos para realizar actividades de PFMEA, DFM y DFA. · ...

Contribute to NPI manufacturing activities associated with the development of TransMedics perfusion set products and OCS products. Apply in-depth knowledge and experience as technical contributor for NPI Manufacturing activities for new product development initiatives. · ...

Lead PFMEA activities in coordination with product development, quality, and manufacturing engineering teams. · ...

Mercury Systems is seeking the best and brightest talent to help us bring cutting-edge technology to mission-critical aerospace and defense applications advancing innovation where it matters most. We bridge commercial innovation with defense-grade security to ensure our warfighte ...

The individual will be responsible for the quality review and approval of validation and change control documentation such as protocols test plans various computer validation testing documents deviations and change controls in relation to DI remediation activities.The documentati ...

The individual will be responsible for the quality review and approval of validation and change control documentation such as protocols, test plans, various computer validation testing documents, deviations, · and change controls in relation to DI remediation activities.The docum ...

JOIN AN INDUSTRY LEADER Quality First & Green Always. · Sloan is the world's leading manufacturer of commercial plumbing systems and has been in operation since 1906. We are at the forefront of the green building movement and provide sustainable restroom solutions. We manufacture ...

The individual will provide Quality Assurance oversight in support of a site product enabling engineering project. · The documentation will span the breadth of validation and change control requirements for biopharmaceutical processing and Quality Control (QC) instruments. · Ensu ...

The GMP Liquid Dose Manufacturing (LDM) implements and maintains various equipment systems in support of the manufacture of clinical biologic drug products. · Manage the qualification effort i.e. coordination of materials and equipment · Generate all necessary electronic protocol ...

The individual will provide Quality Assurance oversight in support of a site product enabling engineering project. · The individual will be responsible for the quality review and approval of validation and change control documentation. · Ensure compliance to governing SOPs, valid ...

We are looking for a hard-working mechanical engineer with at least 5 years of experience who can learn quickly and bring a fresh perspective to complex design challenges. In this role you will have hands-on opportunity to design analyze and test complex subsystems. · Mechanical ...

The individual will provide Quality Assurance oversight in support of a site product enabling engineering project. · ...

Lead the development execution and approval of validation master plans validation plans IQ/OQ/PQ protocols and final reports with emphasis on sterilization endotoxin control and microbiology-related processes. · ...

This position will often serve as the contact person with the client, other design professionals, and contractors. · ...

The Manufacturing Engineer III will lead the development and execution of validation master plans and protocols. · ...

· Overview · As a fully competent engineer in all conventional aspects of the subject matter of the functional area of the assignments, plans and conduct work require judgment in the independent evaluation, selection and substantial adaptation and modification of standard techni ...

· Company Description · US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website · We are constantly on the lookout for professionals to fulfill ...

· Qualifications · ASEE (or ASET) with 5+ years' experience in electrical engineering. · Experience with product safety standards requirements, preferably for medical devices. · Highly motivated and passionate technician with attention to details and having the ability to get th ...

Lead the development and execution of validation master plans and protocols to ensure manufacturing readiness and regulatory compliance. · ...

Join Intelas—a Compass One Healthcare company—where your career thrives and your work directly supports patient care. · We support nearly 4,500 healthcare sites nationwide. · ...

Perform planned preventive maintenance and repairs on imaging equipment in compliance with established standards. · Assist with diagnostic imaging cross training of BMET Technicians. · ...