Senior Manufacturing Engineering Specialist, Documentation

Requisition ID 2024-14934
Posting Date 1 month ago(8/7/2024 10:21 AM)
Job Location(s)
Spencer IN United States
Job Locations
US-IN-Spencer | US-IN-Bloomington | US-IN-Ellettsville
Travel
20-30%
Position Type
Full Time
Company
Cook Inc - Spencer
Category
Engineering

Overview

The Senior Manufacturing Engineering Specialist works to support the manufacturing engineering teams across CINC with project
deliverables including prototype management, documentation and testing. Work within an interdisciplinary team of engineers,
specialists, and technicians, and with other functions, to advance the strategic goals of the company

Responsibilities

- Independently produce, organize, and maintain documentation or systems critical to the function of the engineering team or department.
- Support short-term, long-term, and/or system-focused projects, or complete significant tasks critical to Cook, Inc projects.
- Installs and qualifies equipment in the production areas.
- Develop or revise documents and procedures such as Drawings, Work Instructions, and Standard Operating Procedures
- Prepare prototype work orders, develop manufacturing documentation, perform testing associated with manufacturing projects.
- Drive creation and implementation priority change orders within AgilePLM.
- Ability to work on multiple projects simultaneously, supporting documentation.
- Troubleshoot systems, and/or documentation issues, as needed.
- Use judgment and experience to independently accomplish project objectives.
- Maintain high knowledge level related to the team's focus and relevant company systems (Including jBase, AgilePLM, Opcenter).
- Serve as a mentor, trainer, and resource to the team within area of expertise.
- Identify areas for improvement and offer solutions.
- Prioritize work based on assigned goals
- Read, comprehend and follow product and packaging specifications and manufacturing instructions and drawings.
- Must maintain all training requirements for the position, while seeking out opportunities for continuous development and growth.
- Adhere to the Quality Management System and its processes to meet FDA 21 CFR 820, ISO 13485, and other applicable regulatory
requirements.


- 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 and ability to work in a collaborative and independent work situations and environments with
minimal supervision.
- Ability to remain calm and receptive in fast paced situations.

 

Qualifications

- AS or BS degree in relevant field; or experience of such kind and amount as to provide a comparable background.
- 7+ years experience that relates directly to the above essential job functions/duties.
- Experience working independently and with minimal supervision.
- Working knowledge of Microsoft Office Software (ie: Word, Excel) and AgilePLM.

 

Physical Requirements:

• Personal protective equipment including safety glasses, lab coat and gloves required in some areas associated with this position.
• Sitting for extended periods, utilizes close visual acuity for working with computers, etc.
• Works under general office environmental conditions.
• Moderate exposure to noise level in the work environment that is moderate to occasionally loud.
• Occasionally lifts and/or moves up to 50 pounds
• Frequently required to stand, walk, use hands to grasp, carry, feel or touch; reach with hands and arms; talk and communicate.

 

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