Quality Assurance Associate - Start Now

Quality Assurance Associate -Permanent Full-time role at Pharmavet

Pharmavet

Antimony Street,Carole Park

Manufacturing> Quality Assurance and Control

Full time

About Pharmavet

Australian Pharmavet Contract Manufacturing Pty Ltd (Pharmavet) has an inherent competitive advantage in Production Planning, Operations and Quality Assurance deliverables in line with industry standards. Pharmavet is a fully accredited APVMA licenced manufacturing facility and holder of a schedule 4 drug manufacturing licence.

We are a small group of collective like-minded individuals who love to chase big goals and have fun along the way. With an unrelenting focus on growth, continuous improvement, and commitment to our team members, Pharmavet provides real opportunities for passionate, high achieving people who bring their authentic self to work. We are continuing to build our high-performing team, that has collaboration, transparency, and an innovative mindset, at the heart of everything they do. 

Pharmavet is a rapidly growing Animal Health organization, and its employees are the core of its growth. We’re a young, progressive, and autonomous organization.

Why join Pharmavet?

Embark on a Meaningful Journey: Be a part of a company dedicated to improving animal health through cutting-edge pharmaceutical solutions.

Stay at the Forefront: Stay ahead of industry trends and regulations, continually enhancing your skills and knowledge.

Collaborative Culture: Join a team that values open communication, innovation, and mutual respect.

Diverse Responsibilities: Your role spans from document control to leading CAPA initiatives, ensuring every day brings new challenges and opportunities for growth.

Are you ready to elevate your career in the dynamic world of pharmaceuticals? We're on the lookout for a passionate and detail-oriented individual to join our team as a Quality Assurance Associate. 

Key Responsibilities include but not limited to:

Document Control:

Dive into the heart of our document management system, playing a crucial role in shaping our quality procedures. Your expertise will drive the preparation and revision of essential quality documents.

Non-Conformance, Deviations, Complaints, and Recalls:

Be the first line of defence against quality challenges, ensuring timely reporting and resolution.

Your investigations will play a pivotal role in maintaining the integrity of our products.

Corrective and Preventive Action:

Lead CAPA initiatives like a maestro, investigating, planning, implementing, and ensuring GMP standards are met.

Change Management:

Be a change champion, taking ownership of Change Requests and guiding cross-functional teams through the implementation of required changes.

Risk Management:

Your risk assessments will contribute to the foundation of our Quality Management System.

Desired Qualifications and skills:

• Relevant scientific qualifications (eg. Pharmacy / Medical Science / Bio Science).

Experience: 

• Experience of 1-2 years in a sterile/non-sterile manufacturing environment
• Experience in development and maintenance of Quality Systems.
• Experience with regulators of Animal Health (eg. APVMA, TGA).
• Excellent communication and negotiation skills (written and verbal)
•  Strong problem solving and decision-making skills
• Highly organized
• High attention to detail
• Competency with common IT software (MS Word, MS Excel, MS Visio, MS PowerPoint).
• Competency in project and task management

NO Consultants please.