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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.

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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.


SR. PRODUCT MANAGER - Allen, TX

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.


MANUFACTURING ENGINEER - Allen, TX

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.