Job Title: Manufacturing Engineer 2
About the Role:
As a Manufacturing Engineer 2, you will play a crucial role in validating medical device manufacturing processes and ensuring compliance with QMS/Regulatory standards.
Responsibilities:
• Develop and execute Test Method Validations for Test Equipment per current QMS/Regulatory standards.
• Validate and implement medical device manufacturing processes as assigned.
• Identify equipment/fixture installation qualification requirements.
• Characterization of processes and their outputs/acceptance criteria.
• Prepare written validation reports that meet regulatory/company standards.
• Project management skills to manage multiple projects simultaneously and work with minimal supervision.
Requirements:
To be successful in this role, you will need:
• A Bachelor's degree in engineering or a related field (desired)
• Minimum of 3 years' experience in Validation/relevant experience
• Strong interpersonal and organisational skills and the ability to communicate at all levels of the organisation.
• Willingness to seek out and drive improvement.
• Proven project planning skills and the ability to execute projects in a timely and effective manner.
What We Offer:
We offer a range of benefits including a Hybrid Work Model, Company sponsored Defined Contribution pension scheme, Medical Health Insurance cover, Life Assurance and Income Protection cover, Educational Assistance, Performance related Bonus, Extensive health & wellness program, Fully equipped gym on site, Paid time off to participate in volunteer activities, Free parking, Subsidised restaurant, Sports & Social club