Job Opportunity
A skilled professional is required to work with a medical device manufacturing client on a contracting basis for an initial 12-month contract.
About the Role
1. Develop and implement process-related continuous improvement initiatives that enhance product quality and optimize equipment effectiveness.
2. Collaborate with personnel to identify and resolve corrective/preventative actions addressing process quality-related manufacturing issues.
3. Systematically solve complex problems and use data to inform decision-making, taking the initiative while demonstrating collaborative and influencing skills essential for cross-functional team contributions.
4. Ensure timely delivery of high-quality products across multiple value streams in a cost-effective manner.
5. Manage and coordinate multiple projects within a matrix environment, including change management through quality systems.
6. Apply troubleshooting expertise to resolve complex equipment, system, and process problems using statistical and analytical methodologies.
Requirements
* A minimum Level 8 B.Sc. or B.Eng. honors degree in Physics/Chemistry/Biological Science or Mechanical/Material/Process Engineering, with a proven track record of delivering results.
* A minimum of 7 years' experience working in a GMP environment as an Engineer.
* Familiarity with process validation in a regulated medical device/pharmaceutical environment.