Top 1 Paragon Biomedical Jobs

Manufacturing Engineer
AMETEK, Inc. —Pierceton, IN
- $100,000 - $115,000 a year
- Anatomy knowledge
- 7 years
- Office

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Manufacturing Engineer

AMETEK, Inc. -
Pierceton, IN

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Job Details

$100,000 - $115,000 a year

Qualifications

Statistics
Mechanical blueprint interpretation
Staff supervision
Blueprint specification interpretation
ISO standards
Quality control statistical data analysis
Windows
GD&T
Metal materials
Statistical analysis
Managing engineering teams
Leading team collaboration initiatives
Quality standards in production
Biomedical regulatory compliance

Full Job Description

Location:

Pierceton, IN, US, 46562

Business Unit: Paragon Medical Orthopedics

Posting Date: Jun 27, 2026

Job Description:

SUMMARY OF POSITION: Responsible for leading the development and improvement of internal transactional and manufacturing processes using lean tools, validation activities, and proactive process control measures. The position will lead and participate in cross-functional teams facilitating all activities associated with process development, process improvement, and new product launches. Leads and supervises the day to day manufacturing engineering team and projects.

ESSENTIAL FUNCTIONS:

Lead and supervise projects and the manufacturing engineering team supporting site on time delivery, continuous improvement (CI) and quality objectives
Manages multiple tasks/projects and schedules priorities for self and manufacturing engineers. Responsible for all manufacturing engineering activities within the department.
Directs team to work with cross-functional teams within site and international case & tray sites in developing or improving processes, new production introduction and new equipment deployment. Will also direct personnel to work with operations and regulatory teams to ensure processes are validated and documented.
Lead process improvement activities for department and site process improvement initiates
Develop and monitor compliance within department to meet internal procedures, ISO and FDA regulations
Effectively and proactively perform continuous improvement on existing processes.
Lead process flow development including value stream mapping, process, and product characteristics.
Lead pFMEA development and team discussions along with managing the risk mitigation activities and testing.
Approve and support engineering test protocol development and reporting for process characterization and process testing.
Oversee machine identification, acquisition, and implementation activities.
Approve and participate in part specific, equipment, and process validation activities.
Support and/or approve the development, documentation, and execution of validation protocols and final reports (Installation Qualifications / Operational Qualification / Process Qualification – IQ/OQ/PQ)
Lead and direct team in support of customer complaint investigations and/or corrective and preventive actions (CAPAs)
Support new product development projects and teams, supply chain development and postproduction meetings, as necessary.
Work proactively with the team to share and establish best practices and lessons learned.
Foster close and productive relationships with manufacturing engineering team, cross-functional counterparts and site management team
Understand, develop, and maintain project schedules for all projects that are within the department.
Serve as point of contact for technical interface between production and engineering
May act as site OpEx leader
Develop performance management and professional development of direct reports including communicating responsibilities and priorities of necessary support to each department. Set goals for each employee and monitor their activity through employee development.
Develop standard operating procedures and systems for departmental operations.
Develop, monitor and report on departmental metrics.
Develop and present updates in management meetings.

EXPERIENCE / EDUCATION:

Bachelor’s degree in Mechanical Engineering or Biomedical Engineering.
Minimum of seven years experience, or education background, with blueprint reading, GD&T, working knowledge of short run process control methods, statistical analysis, DOE, ISO standards and FDA quality system regulations.
Previous experience in a leadership position required.
Windows-based computer knowledge required and working experience with CAD systems preferred.
Knowledge of Design for Manufacturability (DFM) principles, biocompatibility requirements for materials, ISO 13485 and US QSR 21 CFR, Part 820 Medical Devices, and basic understanding of the human anatomy preferred.
Thorough working knowledge of various metal and polymer materials, as well as testing specifications, plant engineering, industrial engineering, manufacturing practices, project management, and lean principles.

SKILLS:

Supervisory and interpersonal skills with the ability to cultivate and maintain cooperation from others.
The ability to develop comprehensive project plans and schedules in support of customer, quality and operations improvement objectives.
Excellent communication skills.
Able to work with minimal supervision and actively participate in a team oriented, continuous improvement, manufacturing environment.
Premiere organizational skills and attention to detail required.
Strong leadership, ability to handle multiple tasks and prioritize in a fast-paced environment.
Strong problem solving, decision making, and process improvement skills.

PHYSICAL DEMANDS AND WORK ENVIRONMENT: The physical demands and work environment characteristics described here are representative of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Physical demands: While performing the duties of this job, the employee is required throughout the workday to stand; walk; sit; use hands to handle objects; reach with hands and arms; stoop; talk or hear. Specific vision abilities required by the job include close vision and may also include color vision; depth perception; and the ability to see print in various sizes and formats. May be required to climb stairs, kneel or crouch. May be regularly required to pull and push up to 15 pounds and occasionally lift boxes up to 25 pounds.
Work environment: Work performed in an office environment. The noise level in the work environment is usually low.

Compensation

Employee Type: Salaried

Currency: USD

Salary Minimum: 100,000

Salary Maximum: 115,000

Incentive: No

Disclaimer: Where a specific pay range is noted, it is a good faith estimate at the time of this posting. The actual salary offered will be based on experience, skills, qualifications, market / business considerations, and geographic location.

For more information on AMETEK's competitive benefits, please click here.

AMETEK, Inc. is a leading global provider of industrial technology solutions serving a diverse set of attractive niche markets with annual sales over $7.5 billion.

AMETEK is committed to making a safer, sustainable, and more productive world a reality. We use differentiated technology solutions to solve our customers’ most complex challenges. We employ 22,000 colleagues, in 35 countries, that are grounded by our core values: Ethics and Integrity, Respect for the Individual, Inclusion, Teamwork, and Social Responsibility. AMETEK is a component of the S&P 500. Visit https://www.ametek.com/careers for more information.

We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class. Individuals who need a reasonable accommodation because of a disability for any part of the employment process should call 1 (866) 263-8359.

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