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Ccm Developer Jobs in Camden, NJ (NOW HIRING)

Senior Quality Engineer Marlton, NJ Hope is Here! Impulse Dynamics (USA), Inc. is a fast-growing ... CCM is a first-of-a-kind, proprietary, life-changing treatment alternative for a vast population of ...

Senior Design Quality Engineer Marlton, NJ Hope is Here! Impulse Dynamics (USA), Inc. is a fast ... CCM is a first-of-a-kind, proprietary, life-changing treatment alternative for a vast population of ...

SmartCOMM Lead Developer

Philadelphia, PA · On-site

$59.50 - $78/hr

SmartCOMM Lead Developer Location: Onsite at Philadelphia This role requires you to have mix of ... Build and maintain reusable artifacts to process high volume data, invoke CCM Tool to compose ...

Electrical Engineer

Marlton, NJ · On-site

$80K - $95K/yr

Electrical Engineer Marlton, NJ Hope is Here! Impulse Dynamics (USA), Inc. is a fast-growing ... CCM is a first-of-a-kind, proprietary, life-changing treatment alternative for a vast population of ...

Electrical Test Engineer Marlton, NJ Hope is Here! Impulse Dynamics (USA), Inc. is a fast-growing ... CCM is a first-of-a-kind, proprietary, life-changing treatment alternative for a vast population of ...

CFD Engineer Specialist

Camden, NJ · On-site

$95K - $115K/yr

Proficient in ANSYS (Fluent, CFX, Workbench), STAR-CCM+, meshing tools, and SpaceClaim * Strong ... Programming skills in Python, C++, or Java for automation and post-processing * Excellent ...

Senior Project Manager

Camden, NJ · On-site

$140K - $165K/yr

Bachelor's degree in Engineering, Project Management, Business Administration, or related technical ... PMP certification preferred; additional credentials such as PE, CCM, or Six Sigma Green/Black Belt ...

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Ccm Developer information

See Camden, NJ salary details

$17

$53

$82

How much do ccm developer jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for ccm developer in Camden, NJ is $53.31, according to ZipRecruiter salary data. Most workers in this role earn between $40.72 and $65.24 per hour, depending on experience, location, and employer.

What is a CCM developer?

CCM Developers are specialized software professionals who design, develop, and implement Customer Communications Management (CCM) solutions. They work with CCM platforms to create, manage, and automate personalized customer communications such as statements, invoices, emails, and other documents. Their role often involves integrating CCM systems with other business applications, ensuring compliance, and enhancing customer engagement through efficient communication processes. CCM Developers typically possess expertise in CCM tools (like OpenText Exstream, Quadient Inspire, or Smart Communications), programming, and document composition.

What are the key skills and qualifications needed to thrive as a CCM developer?

To thrive as a CCM Developer, you need strong programming skills (often in Java or .NET), experience with Customer Communications Management (CCM) platforms like OpenText Exstream or Quadient Inspire, and a solid understanding of document management processes. Familiarity with CCM tools, XML, scripting languages, and sometimes certifications in specific CCM software are typically required. Excellent problem-solving, communication, and teamwork skills help CCM Developers collaborate effectively with business stakeholders and IT teams. These skills ensure the efficient development and management of personalized customer communications, which are critical for customer engagement and regulatory compliance.

What are the main challenges a CCM developer faces when integrating customer communications with existing enterprise systems?

A CCM Developer often encounters challenges related to integrating customer communication management solutions with legacy systems and diverse data sources. Ensuring seamless data flow, maintaining data integrity, and aligning output formats with business requirements can be complex, particularly in large organizations with varied technology stacks. Additionally, balancing compliance, security, and performance while delivering personalized, omnichannel communications requires close collaboration with IT, business analysts, and compliance teams. Staying updated on evolving regulations and customer experience trends also plays a crucial role in overcoming these challenges.

What is the difference between Ccm Developer vs Ccm Analyst?

AspectCcm DeveloperCcm Analyst
Primary RoleDevelops and maintains CCM (Customer Communication Management) software solutionsAnalyzes CCM processes, requirements, and optimizes communication workflows
Skills & CertificationsProgramming, software development, CCM platform knowledgeBusiness analysis, process improvement, CCM system understanding
Work EnvironmentSoftware development teams, IT departmentsBusiness units, communication teams, IT support

While both roles involve CCM technology, Ccm Developers focus on building and coding CCM solutions, whereas Ccm Analysts analyze and improve communication processes. Both roles often collaborate but serve different functions within CCM projects.

What job categories do people searching Ccm Developer jobs in Camden, NJ look for?

The top searched job categories for Ccm Developer jobs in Camden, NJ are:

What cities near Camden, NJ are hiring for Ccm Developer jobs?

Cities near Camden, NJ with the most Ccm Developer job openings:

Infographic showing various Ccm Developer job openings in Camden, NJ as of August 2026, with employment types broken down into 79% Full Time, 8% Part Time, 1% Temporary, and 12% Contract. Highlights an 80% Physical, 5% Hybrid, and 15% Remote job distribution, with an average salary of $110,882 per year, or $53.3 per hour.

$120K - $130K/yr

Full-time

Medical, Retirement, PTO

Re-posted 7 days ago


Job description

Senior Quality Engineer
Marlton, NJ
Hope is Here!
Impulse Dynamics (USA), Inc. is a fast-growing medical device company that has pioneered a new form of therapy for heart failure called Cardiac Contractility Modulation, or CCM TM, which is delivered by the company’s Optimizer® Smart System. CCM is a first-of-a-kind, proprietary, life-changing treatment alternative for a vast population of heart failure patients across the globe. With global headquarters in Marlton, N.J., the company has additional offices in Frankfurt, Germany.
There are 64 million patients struggling with Heart Failure worldwide. When these Heart Failure patients continue to decline despite being on optimum pharmaceutical therapy, they lose hope. The only options down the road are extremely invasive. CCM therapy is an FDA Breakthrough designated solution that is minimally invasive and gives hope back to these patients.
This is not a job, It is a MISSION to help the nearly one million patients (in the United States alone) who are struggling with heart failure and qualify for CCM therapy.
The Sr QE is Responsible for providing QA leadership and partnering with product development with planning, coordinating, and managing the quality assurance (QA) activities associated with PD projects to ensure compliance to internal and external requirements during the development and commercialization of new products and changes for existing products.
Responsible for providing technical leadership in establishing, implementing, and maintaining quality system processes and documentation in compliance with domestic and international regulatory/quality requirements
How You’ll Add Value
  • Design Control Coordinator: works with product development engineering to ensure proper completion of required documentation for design control phases according to the design controls SOP. Ensures the electronic Design History File is maintained.
  • Represent Quality on product development teams to ensure adherence to company quality procedures and applicable US and OUS regulatory requirements and standards.
  • Assure that all applicable elements and product technical standards that are applicable to a design category are effectively incorporated into new designs and into changes to designs. Coordinates with Regulatory Affairs and Product Development to identify the full range of standards for all intended regions for distribution.
  • Ensure completion of Risk Management activities for new and/or modified products and processes, which include risk assessment, occurs in the appropriate phase of the project, authoring risk management plans and reports, facilitating risk assessment activities with no guidance required. Collaborate with risk management team members from regulatory, product development, and medical affairs/clinical to ensure robust and realistic documents are created.
  • Author and maintain all risk documentation required for Impulse Dynamics products.
  • Complete design history file verifications at the end of each design control phase.
  • Support the creation and maintenance of Device Master Records (Technical Dossier) for all products.
  • Review and approve all external Engineering Change Orders provided by the contract manufacturer and assess risk documentation.
  • Review and approve all internal change orders and assess risk documentation.
  • Assist in writing, updating and/or reviewing of procedures and other quality assurance related technical data forms and quality documents.
  • Adhere to QMS requirements outlined in procedures and work instructions.
  • Review validation protocols and reports for GMP compliance and alignment with industry best practices.
  • Assist in carrying out internal quality audits on company systems and documentation.
  • Authors non-conformance reports and initiates and owns corrective actions.
  • Perform investigations using recognized quality engineering tools of non-conformances, customer complaints and corrective actions.
  • Ensures the timely and effective follow-up of all identified or assigned quality issues.
  • Assists in the maintenance of the Quality Management System.
  • Acts as an effective leader or team member in supporting quality disciplines, decisions, and practices.
  • Provide training and support for quality system processes and quality engineering practices to members of the quality group as well as across the organization.
  • Maintains and demonstrates understanding of global standards, regulations, and regulatory bodies to include but not limited to ISO 13485:2016, ISO 14971, 21 CFR part 820, 21 CFR part 812, MDSAP and MDR.
  • Manage the Post Market Engineering system to identify trends and recommend actions.
  • Review every complaint for trends and for linkages to risk management system. Perform updates as needed.
What You’re Bringing with You
  • BS in Engineering or Life Science Field
  • 4-7 years of experience in medical device industry or regulated environment (e.g., ISO 13485:2016, 21 CFR Part 820 and MDSAP) in one of the following functions: Quality Assurance/Quality Engineering and Product Development Engineering
  • Strong communication and organizational skills.
  • Intermediate to advanced knowledge of MS Office Suite (e.g., Word, Excel)
  • Self-starter with high attention to detail and ability to work on multiple projects
  • Demonstrated ability to participate in cross-functional team environment
  • Strong written and verbal communication skills
  • Ability to work independently with little to no supervision
  • Excellent organizational abilities and superior attention to detail
  • Must have high level of interpersonal skills
  • Possesses strong analytical and problem-solving skills
  • Excellent time management skills and project management skills
  • Capability of objective analysis
  • Proactive attitude to address problems
Our Commitment to You
Our hiring process lets you show off the very best version of yourself while learning all about us at the same time. Our recruiting promise is a candidate experience that’s enjoyable, thorough, and fair. That’s our way of inspiring the innovative brightest minds.
Impulse Dynamics has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere—we strive to foster an inclusive culture built around a diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves. We strive to foster an inclusive and diverse team, committed to making a difference.
Equal Opportunity Employer Statement:
Impulse Dynamics is an equal opportunity employer.
Impulse Dynamics is committed to the spirit and letter of all federal, state, and local laws and regulations pertaining to equal opportunity. To provide equal employment and advancement opportunities to all applicants, employment decisions at the company will be based on merit, qualifications, and abilities. The company does not unlawfully discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, genetic information, or other protected status. This policy extends to all terms, conditions, and privileges of employment, as well as the use of all Impulse Dynamics facilities.

Compensation amp; Benefits
Annual Base Salary Range: $ 120,000 - $ 130,000

  • Full Coverage Medical Benefits – Employee + family contribution is 100% covered by Impulse Dynamics.
  • Paid Vacation, floating holidays, and sick time.
  • Paid Holidays
  • 401k Match (up to 6%)
  • Annual bonus eligibility


Unless specifically indicated communicated otherwise in writing, all employees are “at-will” employees. The Company reserves the right to modify the aforementioned terms with appropriate notice and under no circumstance do the above described compensation and benefits constitute a promise to continue them for the duration of an employee’s employment.