Manufacturing Team Lead, Medical Devices – 1st Shift

AMETEK Inc.; Mansfield (MA); On-site; USD 50,000 - 55,000; Full time

Job summary

AMETEK, Inc. in Mansfield, MA is seeking a Manufacturing Team Lead for the 1st shift (7:00 am - 3:30 pm). You will oversee daily operations for assembly, packaging, and distribution of medical devices, directing production associates and ensuring safe, compliant production.

The role requires supervision experience, strong communication, and a focus on quality and training; GMP, ISO, and FDA familiarity are preferred to maintain compliance and performance.

Qualifications

• High School diploma or equivalent.
• Must have transportation to work on-site in Mansfield, MA.
• At least 3 years’ experience in manufacturing operations with medical devices.

Responsibilities

• Accountable for day-to-day manufacturing activities.
• Prepare the production floor for daily production.
• Assist with training manufacturing associates.
• Review training requirements and ensure all training is current.
• Assign labor to meet schedules.
• Work on required manufacturing shop orders/workload.
• Ensure production accuracy and quality.
• Follow manufacturing procedures and quality standards.
• Ensure proper material availability for manufacturing work.
• Complete quality and production reports and records.
• Support process and equipment validation/qualification plans with Engineering.
• Assist in development/scale-up activities and documentation review.
• Collaborate with cross-functional teams including Quality and Development.

Skills

Leadership

Training

Quality standards

Manufacturing

Problem solving

Communication

Teamwork

Documentation

Education

High School diploma

Job description

AMETEK, Inc. in Mansfield, MA is seeking a Manufacturing Team Lead for the 1st shift (7:00 am - 3:30 pm). You will oversee daily operations for assembly, packaging, and distribution of medical devices, directing production associates and ensuring safe, compliant production.

The role requires supervision experience, strong communication, and a focus on quality and training; GMP, ISO, and FDA familiarity are preferred to maintain compliance and performance.