Job Overview
This role entails providing quality assurance support for site activities, ensuring compliance with industry standards and collaborating with cross-functional teams to drive improvements in product and process quality.
Main Responsibilities:
* IDentify and resolve complex exceptions to work assignments.
* Makes decisions related to product quality, including the disposition of non-conforming products.
* Promotes awareness of best practices and makes appropriate daily decisions.
* Evaluates new equipment/processes/chemicals for environmental impact.
* Compiles and analyzes operational, test and validation data.
* Participates directly in new product/technology transfer to ensure compliance to internal and regulatory requirements.
Requirements:
* A bachelor's degree or equivalent in an engineering or science-related field.
* A minimum of 2 years' experience working at an engineering level, ideally within the medical device industry or similar highly-regulated fields.
* Experience with internal and external audit processes.