Manufacturing Engineer II

Getinge; Merrimack (NH); On-site; USD 75,000 - 100,000; Full time

Benefits offered by this job

Health insurance

401k plan with company match

Paid Time Off

Tuition Reimbursement

Life Insurance

Job summary

Getinge Group in Merrimack, NH is seeking a Manufacturing Engineer II to support the commercialized production of medical devices. You will apply process development, lean practices, and CAPA to improve quality, yield, and cycle times in a fast-paced manufacturing setting.

Responsibilities include leading equipment troubleshooting, developing work instructions, performing IQ/OQ/PQ validation, and collaborating with QA, R&D and maintenance teams to resolve issues and drive continuous improvement.

Qualifications

• Bachelor's degree in Engineering or equivalent.
• At least 3 years of manufacturing experience in medical devices preferred.
• Strong problem-solving and data-analysis skills.
• Experience with ISO, FDA familiarity preferred.
• Proficient in MS Office; Minitab preferred.

Responsibilities

• Supports production/manufacturing operations.
• Leads scrap reduction and Lean initiatives.
• Develops work instructions for production transfer.
• Performs process development and validation (IQ/OQ/PQ).
• Executes ECOs and equipment documentation.
• Analyzes test results and supports CAPA activities.

Skills

Troubleshooting (Electro-mechanical)

Lean manufacturing

Data analysis

MS Office

Education

Bachelor’s Degree in Engineering

Tools

CAD/SolidWorks

Minitab

Job description

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Manufacturing Engineer II

Date: Oct 30, 2026

Location: Merrimack, NH, US

Company: Atrium Medical Corporation

Remote Work: 0 days at home (site based)

Salary Range: $75K-$100K plus 8% STIP

With a passion for life

Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers – and to save more lives, we need team players, forward thinkers, and game changers.

Are you looking for an inspiring career? You just found it.

Job Overview

Supports the commercialized production of medical devices. Works within manufacturing engineering functions to provide technical support for the quality of the product, process development, continuous improvement, and process control.

Job Responsibilities and Essential Duties

• Works in team setting and works independently with minimal oversight.
• Supports production / manufacturing.
• Supports / Leads scrap reduction / equipment downtime reduction, and Lean efforts.
• Developed manufacturing methods into work instructions and associated training for transfer into production.
• Develops required maintenance and calibration instructions for manufacturing equipment and creates required equipment documentation.
• Provides higher level assistance for equipment design for producing medical devices and components.
• Perform process development and validation including IQ, OQ, PQ, EAT, & TMV.
• Perform process improvement initiatives.
• Supports / Leads non-conformance investigations, CAPA activity, OOT’s, Customer complaints, PFMECA’s, MES, and equipment troubleshooting.
• Executes complex change orders (ECO’s) related to process and equipment documentation.
• Analyzes and documents test results for development and pilot production runs.
• Generates and manages PSO’s.
• Specifies and executes equipment and tooling verifications and equipment acceptance tests. Contributes to the team effort by accomplishing related tasks as necessary.
• Support business metrics.
• Protocol and report writing.
• Identify, Lead, and Resolve component / supplier related problems.
• Perform other related duties as required.
• Performs data analysis / root cause investigations with data driven approach.
• Bachelor’s Degree in Engineering, or equivalent work experience.
• Three years related manufacturing experience (medical device field is preferred).
• Must be highly skilled in equipment troubleshooting (Electro-mechanical)
• Must possess good problem solving skills and data analysis skillset.
• Demonstrated knowledge of MS Office applications (Word/Excel/PPT) is required (Minitab experience is preferred).

Required Knowledge, Skills and Abilities

• A demonstrated knowledge and understanding of Quality Assurance Methods and good analytical and problem solving skills are required.
• Good analytical and problem solving skills.
• The ability to organize, prioritize and adapt.
• Multi-tasking capabilities in a fast paced environment.
• Experience working with FDA requirements preferred.
• Experience working within a medical manufacturing environment preferred.
• Working knowledge of statistical process control and lean manufacturing preferred.
• Working knowledge of computer aided drawings (CAD / solid works) preferred.
• Excellent communication skills (oral and written)

Supervision/Management Of Others

• Potentially

Internal and External Contacts/Relationships

• Main contacts, internal:
• Manufacturing Engineering Staff
• Operations Management and Staff
• Maintenance / Calibration Staff
• Quality Engineering / QC Staff
• R&D Staff
• Main contacts, external:

Environmental/Safety/Physical Work Conditions

• Most duties are performed in an office/workshop environment.
• Personal Protective Equipment may be required as dictated by environment (e.g. safety glasses).
• Frequent tasks are performed in an ISO Class 8, 7 & 5 cleanrooms. Must be able to gown up and perform tasks in a controlled environment.
• Physical requirements such as lifting items under 50 pounds and light assembly work may be required occasionally.
• Travel is typically not required for this position but may occur.

The physical demands described here are a representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

About us

With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.

Benefits at Getinge

At Getinge, we offer a comprehensive benefits package, which includes:

• Health, Dental, and Vision insurance benefits
• 401k plan with company match
• Paid Time Off
• Wellness initiative & Health Assistance Resources
• Life Insurance
• Short and Long Term Disability Benefits
• Health and Dependent Care Flexible Spending Accounts
• Parental and Caregiver Leave
• Tuition Reimbursement

Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law.Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.