Career Openings
Please no telephone inquiries. Principals only need apply. Recruiters, please be advised that Ideal Consent has a no solicitation policy and we kindly request that you do not contact the company on behalf of any open or future positions.

Submit resumes to

Ideal Consent is an equal opportunity employer.

Public Relations Director

The Public Relations Director will be responsible for the following:
  • Team with advertising, marketing, interactive, and client service departments to drive unified branding work for clients and the agency.
  • Render full scope of PR services: account direction, media relations, internal and external communications, crisis management, community events, and creative brand positioning strategies.
  • Craft and execute strategic plans, messaging, press releases, media tours, editorial work, and speech writing.
  • Oversee departmental staff, including PR Account Manager and PR Intern. Educating, encouraging, and inspiring those around you is a must, leading by example always.
  • Participate in new business efforts.
  • Generate strong earned media on behalf of clients and agency in local, regional, and national news outlets. Strong, demonstrable relationships with reporters are essential.
  • Pitch traditional media - such as television, print, and radio - and new media, such as blogs and web-based interactive news outlets with equal prowess.
  • Track, quantify, and demonstrate results of communications efforts. Oversee ROI measurement system, charting quantitative and qualitative PR values.
  • Generate opportunities to position the agency's expertise within industry and client categories; pursuing guest editorial and leadership positioning possibilities.

6-10 years of agency experience is required. Please provide three relevant writing samples (i.e. strategic plans, press releases, messaging/talking points, or editorial pieces), samples of earned media coverage you generated, and letters of reference or client testimonials. Experience in Health Care a plus.


The Sr. Product Manager will be responsible for the following:
  • Determines and executes appropriate market research needed and interacts with physicians, clinicians, sales force, and R&D staff regarding new products and product enhancements.
  • Analyzes customer requirements and develop recommendations for existing and potential new products, as well as product enhancements.
  • Collects and analyzes information on competitive product offerings, including features, pricing, and treatment indications.
  • Coordinates new product sales forecasting and build plan with operations and sales.
  • Participates in project rationalization decisions for product line(s).
  • Develops programs for physicians and other health professionals involved in the use of our products in order to accelerate the adoption rates of the new techniques and product offerings.
  • Evaluates the opportunities to educate patients on the latest technological advances made by Concentric and the availability of these technologies. 
  • Works closely with sales organization to maximize effectiveness, incorporate feedback into internal initiatives, and provide appropriate tools and strategies.
  • Assists with general marketing activities, e.g., scientific meetings, marketing communications, other promotional activities, etc.
  • Attends relevant scientific and technical meetings and conferences.
  • Ensures appropriate communication processes are established within and across functional groups.  Communicates information related to quality management system effectiveness.
  • Works in accordance with quality system procedures.

Bachelor's degree plus 6+ years of related work experience with a strong understanding of specified functional area, or an equivalent combination of education and work experience. Advanced degree preferred.


The Manufacturing Engineer will be responsible for the following:
  • Provides technical support for daily production, on assigned production lines, by troubleshooting process problems and implementing corrective actions.
  • Monitors process yields and proactively identifies opportunities for manufacturing process improvements on assigned production lines.
  • Leads process improvement efforts on assigned production lines.
  • Conducts process training and certification on assigned production lines.
  • Creates Device Master Record (DMR) documentation, including work instructions for production that are easy to understand and follow. 
  • Provides concurrent engineering support for new product introductions into manufacturing.
  • Specifies, procures and implements manufacturing equipment, tools and fixtures.  Ensures that appropriate inspection and test equipment is obtained and properly used for inspections and tests.
  • Leads design and process validation activities by writing protocols, coordinating validation activities, and writing reports.
  • Designs, performs and documents engineering studies.
  • Supervises and coordinates activities of assigned technicians and contractors.
  • Provides technical support for equipment calibration and maintenance program.
  • Participates in product development team activities including document review, risk analysis, design verification, process validation, design review, and design transfer.
  • Maintains records of task/project status.
  • Ensures appropriate communication processes are established within and across functional groups. Communicates information related to quality management system effectiveness.
  • Works in accordance with quality system procedures.

Bachelors degree in Engineering or equivalent combination of training and experience. Minimum 2 years experience in medical device design, manufacturing or quality engineering.