LINQM is adding a SR Engineer to the team. This is a 6 month project at a minimum.
The right person will have the following experience:
Skills: Top Skills
- Self motivated and high sense of urgency.
- See process through to completion
- Communication and solution based/ resourceful
- Needs to have good understanding of process development and should be very hands-on
The role will be investigating complex manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports.
Identify and ensure the optimization of complex Manufacturing and/or R&D processes using engineering methods (e.g., SIX Sigma and LEAN methods) for design for manufacturing and for continuous process improvement. Identify opportunities for re-design/design of basic equipment, tools, fixtures, etc. to improve manufacturing processes, and reduce risk.
Develop, update, and maintain technical content of risk management files.
Develop training and documentation materials for production (e.g., work instructions) to enable the seamless knowledge transfer of project and manufacturing processes.
Assign support tasks; gives instruction to technicians on conducting tests; trains technicians and provides feedback; and may coordinate technician work.
Possibility of travel if assignment is extended- US travel
The right person: will have medical device experience, 3 years of engineering, and Bachelor's Degree