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PolyNovo

Quality Control Supervisor

Posted 7 Days Ago
Be an Early Applicant
In-Office
Melbourne, Victoria, AUS
Senior level
In-Office
Melbourne, Victoria, AUS
Senior level
The Quality Control Supervisor oversees QC functions, ensuring compliance with standards, managing testing processes, mentoring team members, and supporting regulatory teams.
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Who We Are

PolyNovo is a disruptive medical technology company, headquartered in Melbourne. We design, develop, and manufacture innovative dermal regeneration solutions, using our patented bioabsorbable polymer technology  NovoSorb®. Our lifesaving products have revolutionised the treatment of burns, major trauma as well as multiple emerging indications, and impacted the lives of over 70,000 patients globally.

With a footprint in 46 counties, and 300+ staff across a range of locations, PolyNovo continues to grow and opportunity awaits.

Learn more about PolyNovo by visiting our Website or our LinkedIn page.


About The Role

We are seeking a Quality Control Supervisor who will support the development, implementation, and maintenance of Quality Control (QC) functions throughout our operations. As the Supervisor you’ll act as the lead within the team supporting the day-to-day operations ensuring that things work as they should and escalate as required.

You’ll be responsible for ensuring our products consistently meet required standards and specifications through oversight of key QC activities, including lot release testing, stability studies, environmental monitoring, and incoming material inspections in line with our quality system.

We are looking for someone who brings previous QC experience working in Pharmaceuticals, Medical Devices or General Laboratory and is familiar with working in a regulatory environment.

If this sounds like you, we would love to hear from you!


Responsibilities

  • Support the Quality Control operations and Testers to meet business needs and ensure compliance with regulatory and product quality standards.
  • Perform Testing on incoming, intermediates, and finished goods. Maintain and calibrate QC testing requiment to ensure accuracy and reliability.
  • Support the development and implementation of GMP methods and procedures for inspecting, testing, evaluating the identity, purity, safety of raw materials, intermediates, and finished products, ensuring their conformity to approved specifications and regulatory requirements
  • Prepare, validate and update Test Methods to align with approved standards
  • Participate in the preparation and/or review of protocols and reports for stability testing, new methods development, and third-party analyses.
  • Manage QC documents and records in accordance with GMP practices.
  • Identify and implement improvements for QC processes. 
  • Monitor data trends and recommend corrective actions, as required.
  • Provide technical support to Regulatory, Quality and Manufacturing teams.
  • Assist with investigations into customer complaints and Out-of-Specification results.
  • Mentor and support the development of QC team members.
  • Act as 2IC to Snr QC Manager

About You

  • Bachelor's degree in Chemistry, Biology, or a related scientific field is required. 
  • Minimum 7+ years of experience in a quality control role within the pharmaceutical or medical device industry.
  • Proven ability to supervise, mentor and train junior QC team members
  • Demonstrated experience in method and equipment validation to meet regulatory and quality standards. 
  • Proficient in QC testing methods and equipment
  • Knowledge of analytical equipment software is an advantage (e.g., FTIR, HPLC, GPC)
  • Experience working in GMP or other highly regulated environments.
  • Exposure to polymer-based materials is preferred.
  • Demonstrated ability to work both independently and collaboratively within cross functional teams.
  • Strong analytical skills with a keen attention to detail.
  • Ability to interpret and analyse data to identify sources of variability or error.
  • Excellent problem solving skills and a proactive approach to continuous improvement.
  • Excellent communication and interpersonal skills to support team collaboration.
  • Proven ability to take accountability for the quality and timeliness of their work outputs.
  • Proficient in Microsoft Office suits

Why PolyNovo?

Join a team that values innovation, collaboration, and professional growth. At PolyNovo, we offer a dynamic work environment and the opportunity to contribute to ground-breaking projects that shape the future of our company and the industry.

  • Multinational, ASX 200 listed and values-led business dedicated to redefining healing for the benefit of our patients
  • Unique platform technology, an exciting pipeline of highly innovative products
  • Diverse, inclusive and flexible workplace culture
  • Career development opportunities and unlimited access to online learning
  • Rewards platform with access to discounts at over 450+ Australian retailers
  • Paid parental leave for primary and secondary carers, Nurture Days, and more
  • Salary packaging including novated car leasing.

Apply Today

Please send your resume by clicking on the Apply button. Please note that, due to the high level of interest expected, only shortlisted candidates will be contacted.

We like AI for lots of things… just not résumé review. Your application is read by actual human beings. No automated screening tools are used in our hiring decisions.

Please note only applicants with full working rights in Australia will be considered.

PolyNovo is committed to creating a workplace that values equity, diversity, and inclusion. We recognise and value that it is the sum of our parts – our combined backgrounds, experiences and perspectives – that allow us to succeed.

Learn more about PolyNovo at: https://au.polynovo.com/company/

Top Skills

Ftir
Gmp
Gpc
Hplc
MS Office
HQ

PolyNovo Melbourne, Victoria, AUS Office

2/ 320Lorimer St, Melbourne, Victoria, Australia, 3207

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