Greenwich Compounding Pharmacy

Returning to my roots in community pharmacy on a part time basis  to maintain my clinical knowledge, whilst  I further develop my GMP career outside of traditional pharmacy.

Pharmacist in charge

New Start up - animal health, australia (Pharmadex)

Working with a start up to assist with facility design, QMS development, validation and licensing for non sterile veterinarian product manufacture.

GMP Consultant- Pharmadex

Thermogard 

Working with the NPD team to assist major food and pharmaceutical clients meet their cold chain packaging and sustainability requirements, whilst assisting in new product development. I also developed the company’s ISO: 9001 and HACCP program which is pending implementation.

Packaging engineer and Validation lead

Returning to Waratah Private Hospital on a part time basis post maternity leave, to continuing providing clinical and oncology services to the hospital. Change to part time work involved voluntary relinquishment of pre baby management role.

Clinical Oncology Pharmacist

As the Pharmacy Manager at Waratah Private I was responsible for providing a timely and holistic pharmacy service to the busy rehabilitation hospital. This included the delivery of patient medication, oncology compounding, clinical ward rounds, IVF services, hospital imprest management, antimicrobial stewardship reporting and provision of accurate medication advice to patients and hospital staff.

Hospital Pharmacy Manager - Waratah Private

As part of my employment at HPS Pharmacies I contributed to the design and commissioning of a GMP sterile manufacturing clean room in Western Australia. This involved consulting on facility design to ensure GMP compliance,  involvement in facility commissioning and validation and providing guidance on SOP protocols with a focus on cleaning, sterile gowning and microbial monitoring.

HPS GMP consultant

Planet Protector Packaging

Planet Protector Packaging are inspired to protect our planet and turn waste wool into an amazing insulated packaging option. 

As Head of Pharmaceuticals I played a key role in cold chain qualification from the design phase through to performance qualification and report writing, to ensure a qualified and customised solution is achieved in line with regulatory requirements.

Head of Pharmaceuticals ANZ

Chris O'Brien Lifehouse

Under a short term contract, I assisted the quality team at Chris O’Brien Lifehouse to update the QMS, ensuring all procedures were cGMP compliant for the manufacture of sterile product. This involved the development of validation, SOP and Training documentation, the execution of risk assessment and providing recommendations around cleanroom refurbishments required to meet TGA / GMP compliance.

GMP / Quality consultant (short term contract role)

Verita Pharma Australia

I worked alongside the team at Verita Pharma  to help establish TGA licensed facilities for the manufacture of both sterile and non-sterile pharmaceuticals. This involved facility design, validation development and execution, SOP and process development, team training, risk assessment, liaising with TGA personnel and participation in TGA audit.

GMP and validation consultant

McBeath Health Services

Employed as the original Quality Manager for the business I helped establish the company’s first GMP compliant Quality Management System (QMS), implementing the SOPs that detail the company’s internal processes. Further to this I facilitated the company’s initial and subsequent TGA audits and was contributed to successfully acquiring a TGA license for the manufacture of sterile oncological products.  I was also the project lead in the accreditation of the QMS to ISO: 9001 standards. 

Having established the QMS and after helping secure the TGA manufacturing license, I transitioned from the Quality Department to help co-manage the rapidly growing Production Team. My responsibilities included directing, training and motivating a large cross-functional team of 30 staff and coordinating all aspects of the manufacturing process to ensure a compliant and efficient work environment. Participating in the ongoing review of SOPs and facilitating TGA audits remained key components of this role.

Quality Manager transitioning to Production Manager

Greenwell and Thomas Pharmacy

Experienced in the quality / GMP fields, I am a registered pharmacist with over 15 years’ experience in the pharmaceutical sector. My job roles cover quality management, GMP production management, GMP consulting, IVF, oncology, sterile manufacture, validation, hospital pharmacy management and community pharmacy management.

My work as a Quality Manager, Production Manager and consultant in several TGA licensed manufacturing facilities, instigated my passion for GMP and validation.

Thus, leveraging my technical expertise in these areas, I assist pharmaceutical companies with all areas of GMP compliance. With a focus on cold chain qualification my goal is to help both pharma and food companies achieve an innovative, qualified and sustainable cold chain solution that meets their thermal delivery requirements.

I also continue to work as a clinical pharmacist and actively consult with companies on GMP, sterile manufacture, non sterile manufacture and validation.

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