• • Global Business in medical device industry
  • • 9 month maternity leave contract

We are an International medical device company that develops, supplies and markets high quality, innovative surgical devices – from niche consumables to proprietary surgical instruments – for minimally invasive and open surgery. As well as leading healthcare technology and solutions supplier of high-quality surgical instrumentation, a full line Electrosurgery portfolio.

We currently have an opportunity for an experienced Quality Assurance / Regulatory Affairs Associate to work within a dynamic team. Based in Cheltenham, the role will manage the product development team and closely with product development / design control team to ensure that all technical files meet regulatory, ISO and Quality Management System (QMS) requirements.

Why work with The OR Company

At The OR Company we are dedicated to fostering growth and development and a high performance culture where employee can shine. Our values are Teamwork, Trust, Passion, Excellence, Passion and Innovation which guides are principles for mutual benefit and the ability to add value.

Not only will you benefit by being exposed to all aspects of our business but you will also have access to the following benefits:

  • • Competitive salary package
  • • Reward and Recognition program ‘Preciate’
  • • Team lunches and celebrations
  • • Bonus program
  • • Casual Fridays
  • • Flexibility
  • • Great office with all amenities (South Eastern Suburbs)
  • • Social events (Kick off meetings, team building, Christmas party)
  • • Development plans (e-University)

Role and Responsibility

  • •  Manage and drive processes to obtain regulatory approvals in relevant markets to ensure ORC’s products meet regulatory requirements and approved to be sold in different markets.
  • •  Develop and maintain high level relationships with international partners.
  • •  Manage to ensure products are launched in a timely and professional manner.
  • •  Maintain and ensure continued compliance of the Quality Management System (QMS) in line with ISO 13485, FDA 21CFR820, EU MDD, EU MDR, MDSAP and other regulatory requirements in relevant market.
  • •  Ensure international regulatory requirements are addressed and met. All regulatory projects are planned and documented within the Quality Management System.
  • •  These including product registrations, complaints handling, medical device reporting and product recalls handling.
  • •  To review and implement new relevant requirements for medical devices and our contract manufacturers. Proactively identify compliance gaps and corrective actions that are required to maintain ISO accreditations by TGA and other regulatory bodies, such as US FDA.
  • •  Liaise and develop relationships with all relevant accreditation bodies to establish audits and understand the trends or changes in regulations that will impact company business.
  • •  Ensure all RA payments to government or regulatory bodies are made by the required dates in conjunction with the Finance Manager.
  • •  Managing with a sense of urgency the internal and external processes associated with submitting regulatory applications to the appropriate authorities, and maintaining regulatory approvals. This includes working internally and on clinical trials and liaising with external contact manufacturers to obtain the appropriate registration in areas of contracts partner/potential partners.
  • •  Managing and maintain all regulatory registrations in accordance with the latest standards (e.g. FDA Registrations).
  • •  Assist in the process of reporting and preparing submissions to a high standard for Adverse Events Reporting.
  • •  Manage customer complaints processes.
  • •  Update and maintain regulatory documentation pertaining to QMS of the company based on ISO 13485 and relevant regulatory standards / legislations.
  • •  Complete Product Release Checklists and crosscheck before sign off on manufactured product.

Key Work/Behavioural Competencies

  • •  Demonstrated flexibility, including an ability to respond quickly and decisively to the changing requirements.
  • •  Adaptability, including the ability to learn quickly and proactively initiate action in a dynamic environment.
  • •  Problem solving, ensuring that all key stakeholders are part of the solution.
  • •  Strategic and analytical thinker, with a can do, must do attitude.
  • •  Strong customer focus.

Education and Experience

  • • Proven organizational, prioritization and planning skills.
  • • Strong administration skills – organised, attention to detail and ability to multi-task
  • • Ability to work under pressure and to meet deadlines.
  • • Ability to manage all aspects of the Regulatory Affairs as required by Regulatory / Notified Bodies based on relevant regulatory standards and legislations
  • • Ability to use initiative and learn a new industry.
  • • Understand the importance of urgency on customer complaints, adverse event reporting and product recalls.
  • • Intermediate to advanced skills using Microsoft Office including Microsoft Outlook, Word, Excel, PowerPoint and Adobe, some CRM experience.
  • • Minimum of 3 years’ experience in a similar role.

Package based on experience.

To apply, please email your resume to careers@theorcompany.com.


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