Manufacturing Engineer I

CooperSurgical

Trumbull (CT)

On-site

USD 65,000 - 90,000

Full time

14 days+

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Job summary

CooperSurgical is seeking a Manufacturing Engineer I to optimize production processes for medical devices. You will contribute to sustaining activities and continuous improvement, driving lean methods to reduce costs and improve quality across manufacturing.

In this role you’ll partner with production, quality, product engineering, and regulatory teams to implement changes, validate processes, and support equipment and calibration activities on the shop floor. Travel may be required.

Qualifications

  • Bachelor’s degree in mechanical or industrial engineering or related field required.

Responsibilities

  • Sustain manufacturing activities including change orders and investigating non-conformances.
  • Design and develop efficient manufacturing processes with focus on quality and cost-effectiveness.
  • Optimize processes for better efficiency, yield, and productivity while complying with regulatory standards.
  • Conduct process validations, capability studies, and root cause analyses.

Skills

Excel (general computer skills)
Problem-solving
Communication skills
Team collaboration

Education

Bachelor’s degree in Mechanical Engineering or Industrial Engineering
Associates degree in related field

Tools

Excel
Word
PowerPoint
Visio

Job description

Scope: The Manufacturing Engineer I is responsible for optimizing manufacturing processes and ensuring the production of high-quality medical devices. The Manufacturing Engineer I will primarily contribute to sustaining activities, as well as continuous improvement initiatives that reduce costs and increase the quality of CooperSurgical’s manufacturing processes. The Manufacturing Engineer I is expected to have strong partnerships with the production, quality, product engineering, and regulatory departments.

Job Description
Scope

The Manufacturing Engineer I is responsible for optimizing manufacturing processes and ensuring the production of high-quality medical devices. The Manufacturing Engineer I will primarily contribute to sustaining activities, as well as continuous improvement initiatives that reduce costs and increase the quality of CooperSurgical’s manufacturing processes. The Manufacturing Engineer I is expected to have strong partnerships with the production, quality, product engineering, and regulatory departments.

Job Summary

The Manufacturing Engineer I at CooperSurgical is responsible for driving manufacturing excellence and optimizing production processes for our medical device and fertility products. The Manufacturing Engineer I plays a critical role in implementing lean principles, improving process efficiency, and fostering a culture of continuous improvement.

Responsibilities
Essential Functions & Accountabilities
  • Sustaining manufacturing activities such as executing change orders for existing products and processes, investigating non-conformances in the product and process, and supporting maintenance and calibration technicians.
  • Design and development of efficient manufacturing processes for medical device products, with a focus on quality, cost-effectiveness, and scalability.
  • Optimize existing manufacturing processes to improve efficiency, yield, and productivity while maintaining compliance with regulatory and quality standards, often using lean manufacturing techniques.
  • Conduct process validations, process capability studies, and root cause analyses to identify and resolve manufacturing issues, implementing corrective actions as needed.
  • Assist in the development of project plans and proposals that include elements such as Gantt charts, cost-benefit analysis, risk assessments, and regulatory strategies.
  • Collaborate with R&D teams to ensure new products are designed for manufacturability, considering assembly methods, equipment selection, and process validation requirements.
  • Contribute to the fostering of a culture of knowledge sharing and professional development.
  • Develop and maintain manufacturing documentation, including work instructions, standard operating procedures, and process control plans, ensuring compliance with regulatory requirements.
  • Support the manufacturing floor via partnering with maintenance engineers and technicians to resolve day-to-day downtime.

Cooper’s management team is committed to the development of and implementation of the quality management system and maintaining its effectiveness by communicating to the organization the importance of meeting customer as well as statutory and regulatory requirements.

Travel

Travel may be required to attend meetings or visit manufacturing sites. Approx. 10-20% travel is expected

Qualifications
Qualifications, Knowledge, Skills and Abilities
  • Bachelor’s degree in mechanical engineering, Industrial Engineering, or a related field.
  • 0-5 years of experience in manufacturing engineering within the medical device or pharmaceutical industry.
  • Introductory knowledge of medical device manufacturing processes.
  • Strong computer skills with the ability to use Excel, Word, PowerPoint, and Visio. Advanced skills preferred.
  • Awareness of Lean Six Sigma concepts, statistical analysis tools (e.g., Minitab), and root cause analysis.
  • Excellent problem-solving skills and the ability to work effectively in a cross-functional team environment.
  • Introductory knowledge of quality and regulatory requirements, such as ISO 13485, FDA QSR, EU MDR and GMP.
  • Proficient project management skills, with the ability to prioritize tasks and manage multiple projects simultaneously.
  • Excellent communication skills, both verbal and written, with the ability to convey complex technical information to diverse audiences.
Work Environment
  • Occasional lifting of up to 35 kilograms may be required.
  • Prolonged sitting in front of a computer is common.
  • Ability to work in uncomfortable positions, when required. For example, when repairing various manufacturing equipment.
Experience
  • 0-5 years of experience in manufacturing engineering within the medical device or pharmaceutical industry.
  • Associates or Bachelor’s degree in mechanical engineering, Industrial Engineering, or a related field.
Education
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