Design Control Specialist

5 days ago

Auckland City, New Zealand Aroa Biosurgery Full time

**Design Control Specialist (Quality)**
- Be part of a growing kiwi success story within a supportive and fun-loving team
- On-site Gym and plenty of Free Parking
- Work in a Diverse and Inclusive Team

**About Aroa
Here at Aroa Biosurgery we're unlocking regenerative healing for every _body. _Maori for ‘understanding’, AROA is making and creating innovative and regenerative healing products that are improving the lives of millions of people around the world. We specialise in developing, manufacturing and exporting new and exciting soft tissue regeneration products utilising our successful Endoformextracellular Matrix (ECM) biomaterial.

We have been on quite a journey here at AROA over the last 12 years and we continue to go form strength to strength each time we hire someone new to our company. We have truly ambitious goals here at AROA and we know that it's our people and the culture of the business that sets us apart from the rest. As a medium sized business, we operate in that lovely space where every person can make a huge impact on the results and future of the business.

We listed on the ASX in July 2020, (in fact, the first company to list on ASX post the COVID-19 breakout) and with an additional capital rise since then (due to investor demand), we’re primed for exponential growth in the coming years

**What you’ll be doing**

We’re looking for a full time Design Control Specialist (Quality) to provide quality oversight for the product development activities, process development activities, risk management activities and project tasks.

**_Key responsibilities: _**
- Provide quality oversight for product development activities, process development activities and risk management activities and tasks
- Ensure and maintain compliance with cGMP and regulations
- Assist the orgnisation to meet its quality and regulatory requirements through the provision of appropriate training and guidance, quality reviews, and identification and resolution of quality issues
- Support continuous improvement for quality system processes
- Contribute to quality initiatives

**What you’ll bring**
- A Bachelor of Engineering, Science, or equivalent
- 2-5 years’ experience working within the medical device industry or similar
- Experience with medical device quality system requirements on design and development, risk management and validations
- Quick learner with a positive attitude
- Able to work within a team environment

You will be a strong communicator with excellent analytical and problem-solving skills.

Based in Airport Oaks with easy access to the motorway, there is plenty of parking available around our offices. Our teams are flexible, with a mix of being in office + working from home. We also have an on-site gym, which is available for individual use, or jump in to one of our bootcamp or yoga classes.

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