Medical Device Tooling Designer/ Process Development Engineer at Akkodis

Akkodis is seeking a Medical Device Tooling Designer/ Process Development Engineer for a twelve- month contract opportunity with a client located in Bloomington, IN. You will be responsible for the designing and optimizing of processes required to manufacture new medical devices, as well as designing tooling/ fixtures. You will identify and evaluate innovative processing options based on product attributes for products, including evaluation based on technical and economic feasibility. You will execute cost-effective systems in order to enhance the speed and quality of processing, and ensure produced items comply with government regulations and industry standards.

Pay/Salary Range: $46.43 to $60.71 per hour depending on experience.

Medical Device Tooling Designer/ Process Development Engineer job responsibilities include:

• Using Creo, you will create designs and tabletop fixtures for manufacturing.

• Working with the drafting team, you will approve and update drawings, and confirm them for compliance.

• You will perform EQ/ tooling qualification, run tests and use tools for calibration of equipment.

• Collaborate in a team of engineers focused on design, development, and implementation of new processes (within Company Medical facilities and/or with third party suppliers) required for the manufacture of new device designs.

• Execute methods needed for efficient and effective process development (design for manufacturing, test method validation, process validation, process capability, lean manufacturing, equipment selection and specification development).

• Utilize a risk-based approach is applied during the development implementation and validation of all processes.

• Responsible for process documentation (PFMEA’s, Production Instructions, Drawings etc.) associated with new products.

• Collaborate with R&D team, Operations, and Production engineering to ensure the effective completion of all activities associated with transfer to manufacturing of an R&D Engineering project / objective.

• Compare costs and benefits when choosing product in-house or supplier selection.

• Define, identify, and procure new equipment for manufacturing processes

• Ability to complete projects within specific time lines and meeting performance expectations.

• Adhere to the Quality Management System and its processes to meet FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements.

• Must maintain all training requirements for the position, while seeking out opportunities for continuous development and growth.

• Must work and interact effectively and professionally with and for others throughout various levels of the global organization. Must strictly adhere to safety requirements. Maintain regular and punctual attendance. Must maintain company quality and quantity standards. Must have effective communication skills, which may include oral or written. Excellent problem-solving skills and ability to work in collaborative and independent work situations and environments with minimal supervision. Ability to remain calm and receptive in fast paced situations.

QUALIFICATIONS:

• PhD, MS, or Bachelor's degree in Engineering, or Engineering Technology; or experience of such kind and amount as to provide a comparable background.

- Experience in process development and creating process validation documents with knowledge in design for manufacturing, statistics and lean manufacturing principles

- Experience in identifying process variation, process capability and evaluation and DOE's.

- Experience commissioning and qualification of new processes – equipment

• Three to five years experience minimum working in medical device or automotive manufacturing or GMP regulated environment

• Knowledge of process validation, equipment setup, design for manufacturing, statistics, manufacturing assembly design and lean manufacturing principles.

• Must have process/ equipment validation and process characterization experience - IQ/ PQ/ OQ.

• Knowledge of medical device quality standards ISO13485/FDA practices, GMP and similar regulated industry standards preferred.

• Experience using analytic skills and problem solving

• Working knowledge of Microsoft Office Software (i.e. Word, Excel, Visio, Power point, MS Project)

• Strong knowledge of 3D Modeling software, Creo preferred but SolidWorks is OK. Minitab is a plus.

If you are interested in these Medical Device Tooling Designer/ Process Development Engineer jobs in Bloomington, IN then please click APPLY NOW. For other opportunities available at Akkodis go to

Equal Opportunity Employer/Veterans/Disabled

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The Company will consider qualified applicants with arrest and conviction records.

Pay Details: $46.43 to $57.14 per hour

Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.

Equal Opportunity Employer/Veterans/Disabled

To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to />
The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:

• The California Fair Chance Act
• Los Angeles City Fair Chance Ordinance
• Los Angeles County Fair Chance Ordinance for Employers
• San Francisco Fair Chance Ordinance