Lead Operator - Packaging 2nd shift

ICU Medical; Southington (CT); On-site; USD 52,000 - 64,000; Full time

Job summary

ICU Medical in Southington, CT seeks a Manufacturing Operator to perform functions across operator levels, coordinate tech services, and ensure efficient shift hand-off. You will process transactions in the MRP system and support quality and engineering projects.

The role requires strong communication, knowledge of quality systems in medical device manufacturing, and the ability to learn new technologies; travel is minimal.

Qualifications

• Must be at least 18 years old.
• High School Diploma or GED with 8–10 years manufacturing experience; Technical Certificate with 5–7 years; or Associate’s Degree with 3–5 years.

Responsibilities

• Perform all functions of all Operator levels.
• Coordinate tech services, form specifications changes, and qualifications.
• Ensure efficient shift hand-off and communication.
• Process required transactions in MRP system.
• Serve as Operator representative for Quality and Engineering projects.
• Ensure scheduling to meet production requirements.
• Provide training and mentorship to Operators.
• Promote and support 5S standards; participate in standards development.
• Model company values and support strategic initiatives.
• Ensure compliance with laws, regulations and company procedures.
• Engage in Environmental, Health and Safety initiatives.

Skills

MS Excel

MS Word

MS Outlook

Verbal and written communication

Critical thinking

Quality systems knowledge

Adaptability to new tech

Education

High School Diploma or GED

Technical Certificate

Associate’s Degree

Tools

MRP system

Job description

Job Description

• Perform all functions of all Operator levels.
• Coordinate tech services, forms specifications changes and qualifications.
• Ensure efficient shift hand-off and communication.
• Process required transactions in MRP system.
• Serve as Operator representative for special Quality and Engineering projects.
• Ensure efficient scheduling to meet production requirements.
• Provide training and mentorship to Operators in area.
• Promote and support 5S standards; participate in further standards development and implementation.
• Serve as a resource to Operators in area; model company values and support strategic initiatives.
• This position is required to assure compliance of Company operations to all applicable laws, regulations and standards, good business practices and company documented procedures (including knowledge of all standards, government occupational health and environmental regulations and statutes related to the site).
• Engage others, promote and participate in Environmental, Health and Safety initiatives, focusing on continuous improvement.
• Perform other related duties as assigned or required.

Essential Duties & Responsibilities

• Perform all functions of all Operator levels.
• Coordinate tech services, forms specifications changes and qualifications.
• Ensure efficient shift hand-off and communication.
• Process required transactions in MRP system.
• Serve as Operator representative for special Quality and Engineering projects.
• Ensure efficient scheduling to meet production requirements.
• Provide training and mentorship to Operators in area.
• Promote and support 5S standards; participate in further standards development and implementation.
• Serve as a resource to Operators in area; model company values and support strategic initiatives.
• This position is required to assure compliance of Company operations to all applicable laws, regulations and standards, good business practices and company documented procedures (including knowledge of all standards, government occupational health and environmental regulations and statutes related to the site).
• Engage others, promote and participate in Environmental, Health and Safety initiatives, focusing on continuous improvement.
• Perform other related duties as assigned or required.

Knowledge & Skills

• Microsoft (Outlook, Excel, Word) and computer experience required.
• Strong verbal and written communication skills.
• Superior critical thinking skills; able to investigate and analyze data to resolve problems.
• Demonstrated knowledge of Quality systems as related to medical device manufacturing.
• Ability to learn new technologies, knowledge of continuous improvement processes.

Minimum Qualifications, Education And Experience

• Must be at least 18 years of age.
• High School Diploma, or GED with 8 to 10 years of manufacturing experience; Technical Certificate with 5 to 7 years of experience; or Associate’s Degree with 3 to 5 years of experience.

Work Environment

• Work involves use of manufacturing equipment or close proximity to equipment. May be exposed to biohazards and/or chemicals.
• Work environment can range from clean room and proper gowning requirements to a production area that is open, potentially noisy and with moving equipment.
• Recurring physical demands include standing, walking, stooping, crouching, climbing, bilateral motion involving hands, wrists and upper body.
• Concentrated visual attention to perform checks on products and components.
• Typically requires travel less than 5% of the time.