Vacancy expired!
Job Description SummaryThe primary function of this role is to assist the Engineers. This includes, but not limited to, reviewing, writing, planning and executing engineering studies, validations, periodic validation assessments, and MSA’s. Strong writing and communication skills are required due to the involvement with leaders. The Engineering Assistant will write protocols, reports, manufacturing/quality documents and work instructions, assist with miscellaneous tasks as needed including product testing and inspections. Projects may span all departments and products within the BDM, PS Columbus East facility. Ensures compliance with BD quality systems, policies, procedures and best practices, and all local, state, federal and BD safety regulations, policies and procedures. Regular, punctual attendance is an essential job function. Ability to read and write and converse in English. Willing and able to uphold BD Values. Job Description
Be part of something bigger!BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues. JG2PCP Level 2 Duties and Responsibilities:- Write, set up, run, evaluate an and the steps related to set-up and operation of manufacturing equipment.
- May write, execute, and track Engineering Work Orders, CIRs, or ACRs.
- Fill administrative role for tracking systems, as required.
- Material management and logistics of manufacturing product.
- Assist with customer quality complaints as needed.
- Interpret data using technical software, including Minitab.
- Write / Review manufacturing documents, including, but not limited to Manufacturing Operator Instructions, Test Procedures, Quality Control Documents, CAPA’s, OOS Calibrations, PM’s, Audits Reports, FMEA’s, and Design Specifications.
- Assist in the execution of engineering tests and product inspections.
- Cooperate and work in harmony with others, including co-workers, management and technical associates.
- Comply with all policies, procedures, team norms and work rules.
- Comply with all safety rules and regulations and the job safety analysis.
- Follow plant safety and environmental rules and procedures and cooperate fully with the safety and environmental programs(s).
- Other duties as required to support the needs of the business.
- 3-5 years working in a manufacturing environment; medical device manufacturing experience preferred.
- 2-3 years manufacturing experience that required knowledge of quality processes.
- Degree level qualification; or equivalent combination of education and experience.
- Preferred demonstrated success:
- Writing, setting up, running, evaluating and tracking validation and engineering studies, including outline and template validation protocols, reports, and interpreting date; experience with molding, assembly and packaging validations preferred.
- Using SPC
- Using comparator, micrometer, indicator gauges, and computer interface
- Interpreting readings from gauges, micrometers and indicators
- $0 payroll contributions if your salary is below $50,000
- Plan covers 100% preventative care (annual wellness exam, and immunizations)
- Visit any provider
- Competitive pay
- Up to 6 weeks of paid parental leave
- Medical, dental, and vision insurance plans
- Education assistance ($5250.00 per year)
- Adoption assistance
- 401K plan with $.75 of every dollar matched up to 6% of compensation
- Basic life and AD&D provided
- Discounted home, auto, and pet insurance plans
- Paid holidays and vacation (pro-rated the first year based on actual start date)
Vacancy expired!