Job Description

Work Flexibility: Onsite

Manufacturing Engineer - Stryker Anngrove

(Initial 12 month FTC)

The Engineer will provide advanced technical and engineering support across operations at our cutting-edge Additive Manufacturing Anngrove. The role will leverage strong engineering expertise and systems knowledge to support manufacturing operations, drive process improvements, and contribute to key projects that enhance operational performance .

Talents we are looking for:

• Strategic thinkers People who enjoy analysing data or trends for the purposes of planning, forecasting, advising, budgeting, reporting, or sales opportunities.
  Collaborative partners People who build and leverage cross-functional relationships to bring together ideas, data, and insights to drive continuous improvement in functions.

• Analytical problem solvers People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues.
  Dedicated achievers People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
  Curious learners People who seek out cutting-edge research and information to expand and enhance their ability to develop new ideas into reality.

What You Will Do

• Application of a prioritised approach in Value Centred Engineering toward achieving key opportunities in quality, service and cost.

• Works with Engineering leaders to deliver business objectives.

• Responsible for assisting in the development of a world class-manufacturing group that is proficient in process improvement and problem solving manufacturing issues using Six-Sigma tools Providing technical leadership on all product and process issues.

• Line performance monitoring, and the compilation and execution of structured event plans to remediate systemic issues that drive sub-optimal performance.

• Development and implementation of appropriate supporting documentation, SOPs and process work instructions compliant with current Good Manufacturing Practices (GMP)

• Leading technical improvements under the business’s Continuous Improvement Program (CIP).

• Process validation for products and processes; VP, IQ, OQ, PQ and associated documentation.

• Responsibility for projects (value stream and cross functional) as assigned by the company, including the scoping, approval, budgeting, specification, execution, qualification and operational handover as appropriate.

What you will need:

• A level 8 Honours degree in an Engineering discipline.

• 0-2 years’ experience in an FDA regulated manufacturing environment.

• Demonstrable analytical and problem-solving skills, a process improvement orientation, and the ability to handle multiple tasks in a fast-paced and results-oriented environment.

• Excellent presentation and written / verbal communication skills.

• Confident and effective decision maker, with a proven leadership ability to negotiate and influence others.

• Proven Project Management skills through the delivery of business-critical projects.

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Travel Percentage: None