ZipRecruiter

Log In

1

Director Engineering Medical Device Jobs in Connecticut

Pfizer

Director Engineering - Team Lead

Groton, CT

$176K - $294K/yr

The Director Engineering- Team Lead will lead a team responsible for developing AI-enabled ... medical leave, and health benefits to include medical, prescription drug, dental and vision ...

Astrix Inc

Medical Assembler

Bridgeport, CT · On-site

$18/hr

Complete additional tasks or special assignments as directed by management. Qualifications & Skills ... Previous experience in medical device or regulated manufacturing environments is a plus.

ICU Medical

Engineer III, Product Design

Southington, CT · On-site

$131K - $157K/yr

As a subject matter expert (SME) in medical device development, this position will drive key projects of significant complexity while applying sound engineering principles, experimental methods, and ...

ICU Medical

Engineer III, Product Design

Southington, CT · On-site

$131K - $157K/yr

As a subject matter expert (SME) in medical device development, this position will drive key projects of significant complexity while applying sound engineering principles, experimental methods, and ...

Cooper Companies

Manufacturing Engineer I

Trumbull, CT · On-site

$71K - $92K/yr

Bachelor's degree in mechanical engineering, Industrial Engineering, or a related field. * 0-5 years of experience in manufacturing engineering within the medical device or pharmaceutical industry.

PSG Global Solutions

Test Engineer II

North Haven, CT · On-site

Team Player Good engineering/science background Software skills POSITION SUMMARY: A new product ... years of direct involvement with medical device verification. Additional Information All your ...

CooperCompanies

Manufacturing Engineer I

Trumbull, CT · On-site

$71K - $92K/yr

Bachelor's degree in mechanical engineering, Industrial Engineering, or a related field. * 0-5 years of experience in manufacturing engineering within the medical device or pharmaceutical industry.

Cooper Companies

Staff Firmware Engineer

Trumbull, CT · On-site

... medical device industry. * Minimum of Bachelor of Science Degree in Computer Science, Electrical Engineering, Electronics, Robotics, Mechatronics, Computer Engineering or combination of related ...

next page

Showing results 1-20

All JobsEngineering Medical Device JobsDirector Engineering Medical Device JobsDirector Engineering Medical Device Jobs in Connecticut

Director Engineering Medical Device information

What is a director engineering medical device?

A Director of Engineering in the medical device industry leads the design, development, and testing of medical technologies while ensuring compliance with regulatory standards. They manage engineering teams, oversee project timelines, and collaborate with cross-functional departments, including R&D, quality assurance, and manufacturing. Their role involves strategic planning, resource allocation, and risk management to drive innovation and bring safe, effective medical devices to market.

What are the key skills and qualifications needed to thrive in the director engineering medical device position?

To excel as a Director Engineering Medical Device, you need extensive experience in engineering management, regulatory compliance (such as FDA and ISO standards), and a background in medical device design or related technical fields. Proficiency with product lifecycle management (PLM) tools, design control systems, and quality management certifications like Six Sigma or PMP are highly valuable. Outstanding leadership, strategic thinking, and the ability to communicate effectively across multidisciplinary teams help set top performers apart. These capabilities are crucial to successfully guide high-stakes projects, ensure regulatory compliance, and drive innovation in a highly regulated industry.

What are the typical challenges faced by a director of engineering in the medical device industry?

A Director of Engineering in the medical device field often navigates complex regulatory requirements while balancing innovation and speed-to-market. They frequently manage cross-functional teams, oversee rigorous testing and verification processes, and must ensure that all products meet strict quality and safety standards. Collaboration with regulatory, clinical, and marketing teams is essential to align technical development with business objectives. Additionally, adapting to evolving technology and changes in regulatory landscapes can present ongoing challenges, making strong leadership and adaptability key assets.

What are popular job titles related to Director Engineering Medical Device jobs in Connecticut?

For Director Engineering Medical Device jobs in Connecticut, the most frequently searched job titles are:

What job categories do people searching Director Engineering Medical Device jobs in Connecticut look for?

The top searched job categories for Director Engineering Medical Device jobs in Connecticut are:

What cities in Connecticut are hiring for Director Engineering Medical Device jobs?

Cities in Connecticut with the most Director Engineering Medical Device job openings:

Director Engineering Medical Device jobs near you
Infographic showing various Director Engineering Medical Device job openings in Connecticut as of August 2026, with employment types broken down into 80% Full Time, 8% Part Time, 4% Temporary, and 8% Contract. Highlights an 99% In-person, and 1% Hybrid job distribution.

Precision Manufacturing Process Engineer -- Medical Device Machining

TOMZ Manufacturing Corp

Berlin, CT • On-site

$100K - $130K/yr

Other

Posted 6 days ago

Key responsibilities

  • Partner with operations to eliminate equipment and tooling interruptions and support process capability checks.

  • Collaborate with cross-functional teams to transition new products, author engineering change orders, and train operators.

  • Lead root-cause investigations for defects, implement countermeasures, and support continuous improvement initiatives.

Job description

Precision Manufacturing Process Engineer — Medical Device Machining

Location: Berlin, CT

A day in the life

Morning begins on the production floor, partnering with Operations to eliminate equipment and tooling interruptions before they impact delivery. You review tool life studies to uncover cost and efficiency gains, then head to the line to run capability checks that keep processes in control. Midday, you collaborate with cross‑functional teammates to transition a new product toward mid–high volume, authoring and rolling out engineering change orders and training operators on updated work instructions. In the afternoon, you facilitate a PFMEA, qualify equipment through IQ/OQ/PQ, and lead a targeted Kaizen to drive measurable improvements in quality, throughput, and cost. When defects appear, you lead root-cause investigations and implement effective containment and countermeasures. Throughout the day, you uphold the TOMZ Quality Management System.

What you will do
  • Reduce and prevent equipment/tooling downtime and scrap through hands-on support.
  • Run tool life and process capability studies to improve efficiency and reduce cost.
  • Industrialize new products: establish and scale robust, mid–high volume processes.
  • Continuously improve methods and controls for quality, cost, and throughput across sustained and new products.
  • Prepare and deploy ECOs; create and deliver training to operations personnel.
  • Author clear process instructions; optimize product flow, assembly methods, space usage, quality, and safety performance.
  • Develop and qualify manufacturing tools and equipment.
  • Analyze products and processes to identify cost, quality, and efficiency opportunities.
  • Use risk tools (e.g., PFMEA) to identify risks and define corrective actions.
  • Support and execute IQ, OQ, and PQ validations for processes and equipment.
  • Troubleshoot defects, lead investigations to root cause, and implement durable countermeasures.
  • Train Engineering and Operations team members on processes and equipment.
  • Disposition nonconforming product and create rework procedures as needed.
  • Lead Kaizen events and advance continuous improvement initiatives.
  • Follow the TOMZ Quality Management System and perform other duties as assigned.
Qualifications
  • Exceptional attention to detail.
  • Fluent in interpreting drawings and specifications with GD&T.
  • Proficient with SolidWorks.
  • Skilled with Microsoft Office and Adobe tools.
  • Strong grasp of GMP and ISO 13485 requirements.
  • Hands-on experience with Lean/CI, including facilitating or participating in Kaizen events.
  • Comfortable in a fast-paced medical device manufacturing setting with high output and uncompromising quality.
Education
  • Bachelor’s degree in an engineering discipline or equivalent experience.
Experience
  • 5+ years in a regulated industry; medical device or aerospace contract manufacturing preferred.
Preferred skills
  • Strong time management and the ability to prioritize work effectively.
  • Self-motivated; able to contribute independently and in teams.
  • Clear, professional verbal and written communication in English.
Physical requirements
  • Able to bend, stoop, squat, kneel, and lift up to 20 lbs.; team lift or mechanical assist required for items over 20 lbs.
  • 20/20 vision (assisted or unassisted) for sorting raw and nonconforming materials; good manual dexterity for small to medium products.
  • Exposure to oil, grease, dust, metal particles, sparks, and sharp-edged materials; PPE or engineering controls may be required.
  • Frequent keyboard input and computer use.