In this role, you will provides responsible engineering support for GMP (Good Manufacturing Practice) environmentally-controlled chambers, freezers, glass washers, autoclaves and associated support systems within a biopharmaceutical manufacturing plant.
In this role, the selected candidate will be responsible for for product and manufacturing integration development, driving on-time-on-budget releases, and prioritizing all integration feature-function requests and provide detailed requirements.
Participate in product and equipment design reviews for the purpose of developing a robust product and manufacturing process. Prepare and obtain quotes and materials needed for manufacturing equipment changes or improvements.
This position requires supporting engineering and production for a specific product or group of products. Other requisites include interfacing with production, and customer engineering to solve problems. The ultimate goal is to sustain products with repair cost reduction and yields improvements.
Management responsibilities include supervision of design and drafting staff, coordination with clients and associates, and organization of design and construction administration activities to meet established schedules and budgets.
The Quality Engineer will act as a liaison between the customer and the organization in all matters related to quality with respective customers; this position will also ensure that processes and systems are in place that meets the needs of the customer and the business.
In this role, the selected candidate must have experience with manufacturing processes such as extrusion, moulding, die cutting, skiving, punching, drilling, pad printing, hot stamping, and ultrasonic welding.