Senior Manufacturing Engineer - Stryker Anngrove
(Initial 12 month FTC)
The Senior Engineer will play a key role in providing advanced technical and engineering support across operations at our state-of-the-art Additive Manufacturing site in Anngrove. Working across manufacturing and project teams, they will apply their engineering expertise to optimise processes, resolve technical challenges, and support the successful delivery of operational and strategic initiatives.
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.
Goal-oriented developers. Keeping the customer and requirements squarely in focus, people who deliver safe and robust solutions.
User-focused creators. People who imagine with the user in mind, developing technology that helps change patients’ lives.
Responsibilities will include:
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).
Transferring and implementing processes, either from development, or from another manufacturing facility.
Provision of technical leadership/guidance for the Process / maintenance Technicians and other Manufacturing / Equipment Engineers on the team.
Process validation for products and processes; VP, IQ, OQ, PQ and associated documentation.
Conduct Gauge R&R studies for products and new processes.
Carry out structured problem solving.
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.
Actively interfacing with cross-functional team members and 3rd party Vendors, and always practicing good team work in support of the day to day operating requirements, and in pursuit of achieving the business targets
Fostering a work environment of continuous improvement that supports Stryker’s Quality Policy, Quality System, and the appropriate regulations for the area they support, in particular ensuring that employees are trained to do their work and their training is documented.
Observing the Quality Management Systems requirements on site at all times
Continuous monitoring and reporting of variables that feed into the business performance metrics, and pro-active identification and resolution of issues around any deficits in same.
Qualifications, Skills & Knowledge:
Level 8 Degree in Mechanical Engineering or equivalent technical experience is required.
Proven Project Management skills through the delivery of business critical projects.
Has 2-4 years’ experience in a manufacturing environment.
Strong communication and influencing skills with both internal and external agents.
Capable of technical leading, influencing and providing technical direction to Engineers, Coop Students, Technicians and operators as required.
#IJ
Travel Percentage: NoneSkills Required
- Level 8 Degree in Mechanical Engineering or equivalent technical experience
- 2-4 years' experience in a manufacturing environment
- Proven Project Management skills through delivery of business critical projects
- Proficiency in process improvement and problem solving using Six-Sigma tools
- Knowledge and application of current Good Manufacturing Practices (GMP)
- Experience with process validation activities (VP, IQ, OQ, PQ) and associated documentation
- Ability to conduct Gauge R&R studies
- Strong communication and influencing skills with internal and external stakeholders
- Capability to technically lead and provide guidance to engineers, technicians, coop students and operators
Inari Medical Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Inari Medical and has not been reviewed or approved by Inari Medical.
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Fair & Transparent Compensation — Pay is considered competitive for many roles, with employees described as 'extremely happy' with total compensation including pay, stock, equity, and benefits. Feedback suggests above‑average salary levels across departments contribute to strong pay sentiment.
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Healthcare Strength — Benefits include comprehensive medical, dental, and vision coverage, with 100% employer‑paid premiums for employees cited in multiple descriptions. Additional options like critical illness, accident, hospital indemnity, and wellness programs reinforce the healthcare offering.
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Leave & Time Off Breadth — Time off is characterized by unlimited PTO, cited as a top benefit by employees. Paid holidays and flexible hours are also referenced, expanding the range of time‑off options.
Inari Medical Insights
What We Do
Inari Medical, Inc. is a commercial-stage medical device company focused on developing products to treat and transform the lives of patients suffering from venous diseases.





