Quality Control Analyst

2 weeks ago

Auckland City, New Zealand Aroa Biosurgery Full time

**Quality Control Analyst (Technical Support)
- Be part of a growing kiwi success story within a supportive and fun-loving team
- On-site Gym and plenty of Free Parking
- Have your birthday off

**About Aroa
Here at Aroa Biosurgery we're unlocking regenerative healing for every _body. _M ā ori 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 Endoform extracellular Matrix (ECM) biomaterial.

We have been on quite a journey here at AROA over the last 12 years and we continue to go from strength to strength each time we hire someone new. We have truly ambitious goals, 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 raise 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 QC Analyst to join our QC Technical Support team.

This role will support various ongoing stability studies, test method and equipment validation within AROA. This includes liaising with suppliers to ensure all equipment within the laboratory is calibrated and ready to use at all times, performing testing of stability samples and general samples received by the laboratory and being involved in various validation activities. You will also work collaboratively in cross functional team settings.

**Key responsibilities:
- Ensure lab cleanliness and safety standards are maintained.
- Ensure QC equipment is calibrated by performing in-house equipment calibration and organising external calibration.
- Monitor QC lab consumable inventory and perform stock take.
- Perform QC testing activities for finished product and raw material testing, validation and stability study samples.
- Accurately check data produced during testing and record the original data.
- Ensure out-of-spec results are documented and investigated via Laboratory Investigation Reports and/or Non-Conformance Reports.
- Write technical documents such as, but not limited to test method validation protocols, equipment IQOQ and justification reports.
- Lead validation activities such as equipment qualification, test method and software validation.
- Collaborate and assist various teams with compliance and validation activities.
- Liaise closely with other team members to ensure all work is completed accurately and efficiently.
- Demonstrate compliance with GMP standards and quality systems through leadership.

**What you’ll bring
- A tertiary qualification in Bachelor of Science or equivalent.
- 3 years of related experience, 4 or more years is advantageous.
- Microbiology, biochemical or biophysical testing experience.
- Experience in equipment calibration and maintenance is desirable.
- Strong technical writing skills and experience in authoring various validation protocols.
- Excellent English written and verbal communication skills.
- Experience with MS Word and Excel (MiniTab experience is highly desirable).
- Critical thinking skills with the ability to work independently.
- Validation mindset and continuous improvement approach.
- A collaborative working approach and the ability to work well with people of all backgrounds.

Based in Airport Oaks with easy access to the motorway, there is plenty of parking available around our offices. 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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