Medical Device, Quality/Risk Management, Submission & Registration
4 Year Degree
Acumed is enthusastic about bringing a talented Regulatory professional onto the team!
Acumed is a global leader of innovative orthopaedic and medical solutions developed to improve patient care. With over three decades of experience in the orthopaedic industry, our mission is to aid the afflicted through the ingenuity of our minds, the labor of our hands and the compassion of our hearts. The company is headquartered in Hillsboro, Oregon with a global sales and distribution network supported by offices worldwide.
The Regulatory Specialist helps create, develop and maintain materials needed for regulatory compliance. Assists with company compliance activities, new product submissions, listings, and registration of medical devices.
Understands regulations, follows complex directions, and investigates when clarification is needed.
Initiates International product registration, including renewals or changes and certificates for foreign governments
Manages correspondence with the regulatory and standards agencies or organizations such as FDA, MDD Notified Body, Health Canada, Medimark
Prepares, organizes, and coordinates data for submission to the FDA or regulatory agencies (e.g. 510(k), MDD Technical Files, etc.)
Participates in the preparation and execution of ISO and FDA audits
Assures regulatory compliance and content accuracy of Technical Files and 510(k) files
Completes the duties described in the Quality Manual Converts and/or approves ECRs/ECOs requiring regulatory review
Assists in package insert (instructions for use) development, organization and application
Assists in determination of appropriate safety, regulatory, evaluation and testing requirements for new and approved products
Product development design review team and risk team contributor, providing regulatory/compliance perspective and expertise, to assure products are in compliance with relevant US and foreign standards, codes and regulations
Reports standards changes and summarizes impact on Acumed products
Involvement in new country/market registration as required
Assists in labeling (e.g. package inserts/IFUs(instructions for use), marketing materials, package labels, etc.) development, organization, application and/or review
Assists in development of company regulatory strategies and determine priorities with Sales & Marketing, Engineering and Quality
Reports standards changes, determines impact and takes appropriate action
Bachelor of Science in Biology, Chemistry or related field required
Knowledge of applicable FDA, CMDCAS, ISO, and MDD requirements and consensus standards
2 - 5+ years of regulatory experience
Ability to support product development projects
Experience in the medical device industry or related industry (quality, regulatory, or orthopedic engineering) is preferred
Acumed and ACUTE are equal opportunity employers. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with a disability.
As an equal opportunity employer, Acumed is committed to providing reasonable accommodations to applicants with disabilities. If you are interested in applying to Acumed and need special assistance or accommodation, please contact us email@example.com.
Internal Number: 527
A Company Built on Ingenuity, Hard Work, and Compassion
What started as a small family business in 1988 has since evolved into a global market leader, providing orthopaedic and medical solutions that improve patient care around the world.
The Acumed story begins in Butler, NJ, where Mary and Randy Huebner founded Accurate Machine and Design, also known as Acumed. With only one machinist on staff, Acumed was contracted to engineer implant prototypes for some of the biggest names in the industry.
After relocating to Oregon in 1991, we launched our first line of arthroscopy screws intended for ACL ligaments and haven’t looked back since. The successes of the Oregon Fixation Screw allowed Acumed to research, design, and manufacture the majority of our products while adding new lines each year. In 1999, Acumed became a member of The Marmon Group and subsequently, in 2002, a member of the Colson Associates group of companies.
Headquartered in Hillsboro, Oregon, with a global distribution network and offices worldwide, Acumed is a multi-award-winning company dedicated to innovative and quality medical device solutions. We are committed to the highest standards of manufacturing... and proudly produce over 90% of our implants in the U.S.
Throughout our history, Acumed has remained focused on the founders’ original vision of providing innovative solutions to meet the needs of the whole healthcare community, including hospitals, surgeons, and patients.