Work closely with Engineering, Commercial/Sales, Sourcing, and Production to develop comprehensive cost estimates and quotations for medical device manufacturing projects, considering location, materials, labor, overhead, and any additional costs.
Work closely with engineering, production, and sales teams to understand project feasibility and ensure alignment with manufacturing capabilities.
Maintain accurate records of quotations, project specifications, and client communications for future reference and auditing purposes.
Ensure that all quotations comply with relevant medical device regulations and quality standards.
Contribute to the development and refinement of quoting processes, tools, and templates to enhance efficiency and accuracy.
Develop and update process documentation including assembly procedures, test procedures, BOMs, process flows, and process FMEAs.
Produce products that conform to the company documentation and Quality Management System (QMS) standards.
Recommend formats responsive to technical, operational, quality, and customer requirements.
Support and implement company goals and objectives, policies and procedures, Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), FDA QSR and ISO regulations.
Demonstrate all of Ingersoll Rand s corporate values.
Other duties as assigned by the Director of Engineering

Mandatory Skills

Exceptional analytical skills with the ability to interpret technical specifications and cost data.
Excellent verbal and written communication skills; ability to present complex information clearly and persuasively
Must meet internal deadlines and customer due dates
Must be detail oriented, focused, and committed to delivering produce accurate and high quality work
Must have advanced skills in Microsoft Word, Excel, PowerPoint.
Proficient in CAD software including SolidWorks

Desired skills:

3+ years experience in quotation or estimating role, or manufacturing engineering experience
Experience with manufacturing medical devices and associated regulatory requirements
Strong understanding of manufacturing processes and material used in medical device production.
Experience with product qualification and process validation activities

Basic Qualifications

Bachelor of science in Engineering, Manufacturing, or related technical field
3+ years experience in manufacturing engineering or a related field
Must be motivated and creative, work well under pressure and operate effectively in a fast paced team environment.

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