Top 11 Biomedical manager Jobs in Westfield Ma

Biomedical Engineer
Oxford Performance Materials —South Windsor, CT
- $65,000 - $75,000 a year
- Full-time
- Anatomy knowledge
- Microsoft Excel
- Engineering
- Health savings account
- Health insurance
Quick Apply
THCE Clinical Engineering Manager
Trinity Health —Hartford, CT
- $98,240 - $147,360 a year
- Full-time
- Microsoft Word
- 7 years
- Microsoft Outlook
- Opportunities for advancement
THCE Biomedical Equipment Technician I
Trinity Health —Hartford, CT
- $24.53 - $36.79 an hour
- Full-time
- Anatomy knowledge
- Hospital
- Computer literacy
THCE Senior Imaging Equipment Specialist
Trinity Health —Hartford, CT
- $47.23 - $70.84 an hour
- Full-time
- Anatomy knowledge
- Hospital
- Customer service
Senior Medical Science Liaison (Nephrology) - Lower Manhattan, Brooklyn, Staten Island, Long Island
Vertex Pharmaceuticals —United States
- $171,300 - $256,900 a year
- Full-time
- English
- Mentoring
- Data entry
- Loan repayment program
- Health insurance

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THCE Clinical Engineering Manager
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THCE Biomedical Equipment Technician I
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Working knowledge and ability to use basic hand tools and test equipment specific to the field. Performs Corrective Maintenance (CM) procedures including…
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Biomedical Engineer

Oxford Performance Materials -
South Windsor, CT

Quick Apply

Job Details

Full-time
$65,000 - $75,000 a year

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Parental leave
Employee assistance program
Vision insurance
Life insurance

Qualifications

Anatomy knowledge
CAD design (engineering design task)
Biomedical regulatory compliance
Productivity software
Technical Proficiency
Data analysis software

Full Job Description

Position Summary:

The Biomedical Engineer will support the development, maintenance, and regulatory compliance of OPM’s medical devices. This role combines engineering and quality/compliance responsibilities to ensure devices meet performance, safety, and regulatory standards throughout the product lifecycle.

This position offers the opportunity to gain hands-on experience across both technical engineering functions and regulatory compliance processes, while collaborating with cross-functional teams including Quality, Design, and Manufacturing. The ideal candidate demonstrates strong critical thinking capabilities, exercises independent judgment while maintaining rigorous attention to detail, utilizes data-informed analysis to support continuous engineering and compliance improvements, and is motivated to grow within the medical device industry.

Responsibilities:

Manage case documentation, design controls, and compliance activities for custom medical devices across multiple regulatory markets.
Conduct design reviews, analyze custom device trends, and collect data for performance metrics.
Develop well-structured Technical Memos to support design controls, compliance activities, and cross-functional decision-making.
Oversee Post-Market Clinical Follow-Up (PMCF), customer feedback, and author regulatory reports including periodic safety update reports (PSURs).
Support Engineering Change Orders (ECOs) and implement continuous improvements in safety, quality, and scrap reduction.
Support and execute engineering studies, including development of study plans and coordination of test activities.
Author test protocols and technical reports to document study objectives, methodologies, results, and conclusions.
Support annual FMEA reviews and perform root cause analysis for complaints and nonconformance investigations.
Maintain and update QMS documentation, including revisions, redlines, and procedure updates.
Collaborate cross-functionally to ensure engineering and compliance solutions meet regulatory and quality standards.

Secondary Job Functions:

Assist with verification and validation (V&V) activities to ensure product performance and compliance with design and regulatory requirements.
Support Corrective and Preventive Action (CAPA) activities, including investigation, root cause analysis, and implementation of corrective actions.
Provide support for preparation and maintenance of regulatory documentation as required.
Provide Engineering and Compliance support for other product lines as needed.
Collaborate with cross-functional teams to ensure testing and documentation activities align with quality system and regulatory standards.
Performs other related duties as assigned by manager.

Requirements:

Bachelor’s degree in Engineering, Science, or related discipline (Biomedical Engineering preferred).
Understanding of human anatomy and physiology to support design, compliance, and clinical assessment activities.
Minimum of 1-3 years of experience in a regulated medical device environment (ISO 13485, FDA, or equivalent), or equivalent professional experience.
Excellent verbal and written communication skills.
Demonstrated ability to manage multiple priorities in a fast-paced, regulated environment.
Strong organizational skills with the ability to work independently and meet deadlines.
Proficiency in data analysis tools (e.g., Excel, MiniTab) as well as CAD software/SOLIDWORKS; must know how to use Microsoft Suite (e.g., Excel, Word, PowerPoint)

Pay: $65,000.00 - $75,000.00 per year

Benefits:

401(k)
Dental insurance
Employee assistance program
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Parental leave
Vision insurance

Work Location: Hybrid remote in South Windsor, CT 06074

Quick Apply

Refine Your Search

biomedical manager jobs in westfield ma

Biomedical Engineer

THCE Clinical Engineering Manager

THCE Biomedical Equipment Technician I

THCE Senior Imaging Equipment Specialist

Senior Medical Science Liaison (Nephrology) - Lower Manhattan, Brooklyn, Staten Island, Long Island

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