About the role
The Quality Associate will assist the Quality Manager in maintaining, monitoring, and updating the Quality System to achieve the company's quality objectives.
The ideal candidate should have experience in pharmaceutical manufacturing and familiarity with related quality systems, including knowledge of the elements required for PIC/S cGMP, Pharmacopeia standards, ISO9001, and ISO 13485. However, a curious nature, attention to detail, and the ability to collaborate effectively with the team will also be highly valued.
Candidates should be critical thinkers and team players who enhance the company's quality systems proactively. This can be achieved through internal audits, participation in process improvement programs, development of internal processes, and collaboration with key partners to ensure high-quality outcomes.
Strong communication skills and a positive contribution to the broader VFV team will also be essential for the applicant.
What you'll be doing Conduct inspections on raw materials and finished products.Maintain specifications and standards for control of raw material, packaging and finished products.Assist in addressing customer complaints and investigations using problem-solving techniques and tools and recommend preventative and corrective actions. Provide technical and quality support and advice to internal stakeholders.Ensure non-conformances are reported and acted upon.Carry out supplier assurance and assessment activities.Support the development and maintenance of quality system metrics for management review. What we're looking for Degree in a scientific discipline or extensive, similar on-the-job experience (Quality Assurance or Compliance).At least 5 years of experience in a Quality Assurance environment, working with manufacturing and GxP regulatory requirements, including FDA regulations.Familiarity with electronic Quality Management Systems Familiarity with product/materials regulatory compliance standards such as REACH and RoHS.Solid understanding of Quality Management Systems ISO 9001:215, ISO13485:2016Strong knowledge of process principles such as Lean Six Sigma.Proactive team player, self -starter and hands-on.Strong knowledge of MS Word, MS Excel, and MS PowerPointHighly organized with excellent attention to detailWhat we offer
At VFV Pty Ltd., we are committed to providing a supportive and rewarding work environment for our employees. We offer a competitive salary, opportunities for career development, and flexibility to ensure you have the possibility to take care of every aspect of your health and wellbeing.
About us
VFV Pty Ltd. is a leading manufacturer of high-quality pharmaceutical and medical devices, serving customers both domestically and globally. With a strong focus on quality, safety, and innovation, we are dedicated to improving the health and well-being of people around the world. Join our team and be a part of our mission to deliver exceptional products and services.
Apply now for this exciting opportunity to become a Quality Associate at VFV Pty Ltd.