Salary: $105k - 125k per year
Reference: 1047846
job summary:
Rapidly growing Medical Device company in the Columbia, SC area is currently in search of a Controls Engineer that has experience with overseeing and implementing new highly automated equipment lines. Automation Controls Engineer should also have experience working with suppliers on tooling validations, developing and leading projects to improve process monitoring, quality and reduce costs. The Controls Engineer will also work within final assembly manufacturing environment(s) and drive early-stage process development and manufacturing optimization to ensure products meet design intent.
location: Eastover, South Carolina
job type: Permanent
salary: $105,000 - 125,000 per year
work hours: 8am to 4pm
education: Bachelors

responsibilities:

• Work within final assembly manufacturing environment(s) and drive early-stage process development and manufacturing optimization to ensure products meet design intent.
• Establish sampling and Quality plans
• Participate and/or lead risk management activities including product and process FMEA.
• Support reliability engineering activities.
• Participate and/or lead validation activities for design, process, or products.
• Development and qualification of test methods for verifications and validations.
• Write and execute study protocols, technical reports, manufacturing work instructions (MWI), validations, reports, batch records, design control and other documents as required.
• Develop and implement manufacturing processes and measurement methods to meet tight tolerance manufacturing requirements and manufacturing scale up.
• Lead development of fixtures, equipment, and automation.
• Interface with contract manufacturers and suppliers.
• Process evaluations and lead process optimization initiatives utilizing tools such as SPC, DOE, PFMEA, and MSA.
• Evaluation and continuous improvement of process capabilities.
• Work with and manage external suppliers, conduct DFM reviews, and go onsite as needed.
• Partners with Quality and Regulatory, R&D, and operations to ensure compliance of the manufacturing processes, provide support, for regulatory filings, and ensure the robustness of the process and raw materials.
• Develop and lead projects to improve process monitoring, quality and reduce costs.
• Conduct root cause failure analysis and corrective action.

LI-AS1

qualifications:

• Experience level: Experienced
• Minimum 9 years of experience
• Education: Bachelors (required)

skills:

• Six Sigma
• Manufacturing
• Lean
• Process Improvement
• Manufacturing
• Manufacturing
• Manufacturing
• Manufacturing
• Manufacturing
• Controls
• Automation
• Automation Anywhere
• Controls

• AutomationAutomation

• Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
  At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
  Pay offered to a successful candidate will be based on several factors including the candidate’s education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
  Applications accepted on ongoing basis until filled.

• Work within final assembly manufacturing environment(s) and drive early-stage process development and manufacturing optimization to ensure products meet design intent.
• Establish sampling and Quality plans
• Participate and/or lead risk management activities including product and process FMEA.
• Support reliability engineering activities.
• Participate and/or lead validation activities for design, process, or products.
• Development and qualification of test methods for verifications and validations.
• Write and execute study protocols, technical reports, manufacturing work instructions (MWI), validations, reports, batch records, design control and other documents as required.
• Develop and implement manufacturing processes and measurement methods to meet tight tolerance manufacturing requirements and manufacturing scale up.
• Lead development of fixtures, equipment, and automation.
• Interface with contract manufacturers and suppliers.
• Process evaluations and lead process optimization initiatives utilizing tools such as SPC, DOE, PFMEA, and MSA.
• Evaluation and continuous improvement of process capabilities.
• Work with and manage external suppliers, conduct DFM reviews, and go onsite as needed.
• Partners with Quality and Regulatory, R&D, and operations to ensure compliance of the manufacturing processes, provide support, for regulatory filings, and ensure the robustness of the process and raw materials.
• Develop and lead projects to improve process monitoring, quality and reduce costs.
• Conduct root cause failure analysis and corrective action