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Medical Device Program Manager Jobs in Newtown, CT

CooperCompanies

Staff Firmware Engineer

Trumbull, CT · On-site

... medical device programs. * Previous technical leadership or program management experience including planning, coordinating, and managing R&D and/or managing development partners and/or cross ...

Cooper Companies

Staff Firmware Engineer

Trumbull, CT · On-site

... medical device programs. * Previous technical leadership or program management experience including planning, coordinating, and managing R&D and/or managing development partners and/or cross ...

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.

Amphenol RF

Program Manager

Danbury, CT · On-site

At Amphenol RF, you can expect a competitive salary and comprehensive benefits (medical, dental ... The Program Manager is responsible for managing customers, projects and programs to meet and exceed ...

Family Options Inc

Program Manager 1

Prospect, CT · On-site

$23 - $25/hr

As a Program Manager, you will play a critical role in program leadership, staff development ... Coordinate medical appointments and healthcare services. * Collaborate with nurses, physicians ...

FAMILY OPTIONS INC

Program Manager 1

Prospect, CT

$23 - $25/hr

Description Program Manager Family Options Inc. Join Our Leadership Team and Make a Meaningful ... Coordinate medical appointments and healthcare services. * Collaborate with nurses, physicians ...

Family Options

Program Manager 1

Prospect, CT · On-site

$23 - $25/hr

Description:Program Manager Family Options Inc. Join Our Leadership Team and Make a Meaningful ... Coordinate medical appointments and healthcare services. * Collaborate with nurses, physicians ...

Leonardo DRS

Senior Program Manager

Danbury, CT · Hybrid

$118K - $119K/yr

Job Summary The Senior Program Manager will manage and direct the daily execution of contract ... We are proud to offer competitive salaries and comprehensive benefits, including medical, dental ...

Family Options

Program Manager 1

Prospect, CT · On-site

$23 - $25/hr

Managing incident and accident reporting. To include proper Agency, state, and federal ... Coordinate the medical needs for individuals in the program. This includes, but is not limited to ...

Marrakech, Inc.

Day Program Manager

West Haven, CT · On-site

$21.37 - $21.82/hr

Join Marrakech as a Day Program Manager Paid Training | Career Growth Make a Difference Every Day ... Supporting medical needs and appointments * Encouraging community involvement and social engagement

Amphenol RF

Senior Program Manager

Danbury, CT · On-site

$118K - $119K/yr

At Amphenol RF, you can expect a competitive salary and comprehensive benefits (medical, dental ... The Senior Program Manager is a key driver of growth within a designated geographic region, you ...

New

Leonardo DRS

Senior Program Manager

Danbury, CT · On-site

$118K - $119K/yr

Job Summary The Senior Program Manager will manage and direct the daily execution of contract ... We are proud to offer competitive salaries and comprehensive benefits, including medical, dental ...

Amphenol RF

Program Manager (Automotive)

Danbury, CT · On-site

At Amphenol RF, you can expect a competitive salary and comprehensive benefits (medical, dental ... The Program Manager directs and coordinates cross functional teams to execute program deliverables ...

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All JobsMedical Device Program JobsMedical Device Program Manager JobsMedical Device Program Manager Jobs in Newtown, CT

Medical Device Program Manager information

See Newtown, CT salary details

$39.7K

$110.7K

$161.7K

How much do medical device program manager jobs pay per year?

As of Aug 26, 2026, the average yearly pay for medical device program manager in Newtown, CT is $110,695.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,900.00 and $136,500.00 per year, depending on experience, location, and employer.

What is a medical device program manager?

A Medical Device Program Manager oversees the planning, development, and execution of projects related to medical devices within a company. They coordinate cross-functional teams, manage timelines, ensure regulatory compliance, and serve as the main point of contact for stakeholders. Their role is crucial in bringing safe and effective medical devices from concept to market, ensuring that all aspects of the program meet quality and regulatory standards. Medical Device Program Managers often work closely with engineering, quality assurance, regulatory affairs, and marketing teams.

How does a medical device program manager typically collaborate with cross-functional teams during product development?

A Medical Device Program Manager works closely with cross-functional teams including engineering, regulatory affairs, quality assurance, manufacturing, and marketing throughout the product development lifecycle. They coordinate timelines, facilitate communication, and resolve conflicts to ensure project milestones are met while maintaining compliance with regulatory standards. Regular meetings and progress updates are essential, as the Program Manager acts as a central point of contact to align various team goals and address issues proactively. This collaborative approach helps streamline development and supports successful product launches.

What are the key skills and qualifications needed to thrive as a medical device program manager, and why are they important?

To thrive as a Medical Device Program Manager, you need a strong background in project management, regulatory compliance, and biomedical engineering or a related field, often supported by a relevant degree and industry experience. Familiarity with project management tools (such as MS Project), quality management systems (QMS), and certifications like PMP or Six Sigma are highly valued. Exceptional leadership, cross-functional communication, and problem-solving skills help drive successful product development and team coordination. These competencies ensure programs meet regulatory standards, stay on schedule, and deliver safe, effective medical devices to market.

What is the difference between Medical Device Program Manager vs Medical Device Quality Engineer?

AspectMedical Device Program ManagerMedical Device Quality Engineer
CredentialsProject management certifications, engineering degreeQuality assurance certifications (e.g., CQE), engineering degree
Work EnvironmentCross-functional teams, project planning, product developmentQuality systems, compliance, testing, and validation
Employer & Industry UsageMedical device companies, manufacturing, R&DRegulatory agencies, manufacturing, quality departments
Search & Comparison IntentManaging projects, product launches, timelinesEnsuring quality, compliance, risk management

The Medical Device Program Manager focuses on overseeing product development projects, coordinating teams, and ensuring timely delivery. In contrast, the Medical Device Quality Engineer concentrates on maintaining quality standards, regulatory compliance, and testing processes. Both roles are essential in the medical device industry but serve different functions within the product lifecycle.

What job categories do people searching Medical Device Program Manager jobs in Newtown, CT look for?

The top searched job categories for Medical Device Program Manager jobs in Newtown, CT are:

What cities near Newtown, CT are hiring for Medical Device Program Manager jobs?

Cities near Newtown, CT with the most Medical Device Program Manager job openings:

Medical Device Program Manager jobs near you

Staff Firmware Engineer

Trumbull, CT • On-site

CooperCompanies
See more jobs at CooperCompaniesexternal

Full-time

Re-posted yesterday

Job description


This is a highly technical role inside the CooperSurgical R&D New Product Development (NPD) group developing firmware and electronics systems in support of various electromechanical product launches. Within the scope of this role are electro-mechanical connected systems and devices associated with In-vitro Fertilization (IVF) and Assisted Reproductive Technologies (ART). This role will also have an opportunity to be involved in activities associated with surgical devices and instruments in a broader women's health field including Obstetrics and Gynecology (OBGYN).
CooperSurgical's purposeful setting of integrated Front-end Innovations and New Product Development provides an exciting opportunity for R&D engineers to be involved in end-to-end product development from a user centric front-end innovation process, via rigorous product development, to market launch.
This is a high-profile specialist role responsible for defining firmware architecture, coding, prototyping, and verifying firmware, electrical and electronics designs for complex product development initiatives. The Staff Firmware Engineer is expected to work independently under limited supervision and will be responsible for entire project workstreams within firmware and electrical engineering domain. This role will provide inputs on R&D technical directions and is expected to collaborate closely with multi-discipline cross- functional teams with significant impact on departmental results. The Engineer in this role is expected to interface and lead development partners and user community to come up with robust designs and solutions.
Responsibilities
  • Formulate and deliver firmware architecture while influencing hardware design; Lead firmware development for complex electromechanical systems. Analyze and simulate design to understand key parameters and sensitivities. Establish design feasibility by testing firmware / hardware and demonstrating statistical capability for critical functions.
  • Drive medical device Software Design Control compliance by ensuring that all applicable safety, quality and regulatory guidelines and policies are followed to develop safe and effective firmware. Drive, coach and/or oversee definition of design inputs (i.e., product requirements) and technical strategies for an adequate verification and validation approach.
  • Design and de-bug firmware and electronics systems which complies to IEC 62304 and other relevant medical device requirements.
  • Create formal Firmware Verification test protocols, run tests, and write Verification test reports.
  • Coach team members and collaborators in design control processes and best practices. Lead and mentor interns and junior engineers. Mentor and provide technical leadership for junior firmware engineers and interns.
  • Aid and drive an effective cross-functional collaboration ensuring timely and efficient delivery of target business outcomes. Accountable to timely project plan deliverables in cross functional teams utilizing CooperSurgical New Product Introduction (NPI) process.
  • Communicate key technical content to parties within and outside of own function (R&D). May have responsibility for communicating with parties external to the organization and manage external development partners to meet project deliverables on time.
  • Work to influence parties within and outside of the technical function at an operational level regarding policies, practices, and procedures.

Drive improvement, refinement and consistent global implementation of firmware / software development procedures and best practices as well as other applicable Design Control guidelines.
Travel:
This role is primarily site based which requires occasional travel relating to cross-functional meetings, vendor visits, training and/or conference attendance
Qualifications
  • Track record and extensive R&D experience relating to firmware in medical device development and integration of complex electro-mechanical systems, mechatronic, robotic and/or IT/connected systems.
  • An outcome focused mindset including process discipline and drive for timely project completion.
  • Excellent interpersonal and effective communication skills with internal and external stakeholders ranging from project engineers and consultants to key opinion leaders and executives.
  • Track record and deep understanding of development approaches and strategies for effective execution and delivery of complex medical device programs.
  • Previous technical leadership or program management experience including planning, coordinating, and managing R&D and/or managing development partners and/or cross-functional technical programs.
  • Medical device development experience with thorough understanding of Design Control guidelines as defined by FDA, MDR, ISO, CSI, and other standards. Ability to translate User Needs to Design Inputs to creating Verification Test protocols, and perform firmware verification testing, and publish Verification Test reports.
  • Hands-on craft skills and experience with building circuits, de-bugging firmware, soldering, fixing, servicing and/or fabricating concepts, fixtures, and prototypes.
  • Proven and hands on experience in coding C/C++ and state machines
  • Proven and hands on experience with peripherals such as USB, SPI, I2C, UART, GPIO etc
  • Solid understanding of analog circuits, signal conditioning, filters, and digital circuit design
  • Proven and hands on experience in control algorithms like PID, floating point filters, etc.
  • Solid understanding and experience with bare metal systems (no OS) and/or embedded OS (e.g. Embedded Linux, FreeRTOS, etc.)
  • Working experience in circuit and layout tools like Altium Schematic Capture.
  • Strong background in hardware/software integration and hardware debugging using appropriate tools and lab instruments.
  • Working knowledge of ARM Cortex-M microcontrollers and their common peripherals. Experience with the implementation of real-time operating systems (FreeRTOS, Zephyr, others)
  • Experience in SPI, I2C, CAN buses.
  • Understanding of statistical methods including Design of Experiments

Work Environment:
  • Handling and working with electrical and mechanical lab equipment
  • Prolonged sitting in front of a computer

Experience:
  • Minimum of 7 years of closely related experience in development of firmware for complex electrical systems in medical device industry.
  • Minimum of Bachelor of Science Degree in Computer Science, Electrical Engineering, Electronics, Robotics, Mechatronics, Computer Engineering or combination of related fields. Advanced degrees are strongly preferred.

Education:
  • Minimum of Bachelor of Science Degree in Computer Science, Electrical Engineering, Electronics, Robotics, Mechatronics, Computer Engineering or combination of related fields. Advanced degrees are strongly preferred.

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