Quality Assurance Associate

Details of the offer

Rare opportunity to join our QA team. If you are currently working for a CRO or Pharma organisation in QA then we'd love to hear from you.Who are we?We're Avance Clinical, an Australian-based Contract Research Organisation. We offer specialised services supporting drug development for the pharmaceutical and biotechnology industry.Why should you join Avance Clinical?We offer a fun, friendly work environment and a culture that values honesty and respect. We have a strong sense of team & support. We've doubled in size in the last 2.5 years and have promoted over 25% of our people in the last 12 months.The roleThe Quality Assurance (QA) Associate is responsible for supporting the development, implementation, and maintenance of the quality assurance program and related policies and procedures to ensure compliance with Good Clinical Practices (GCP) and other regulations.ResponsibilitiesConduct internal study audits (TMFs, Study Databases & CSR's) to ensure compliance with applicable regulatory and organisational procedures.Conduct internal process audits to verify compliance with internal processes and applicable regulatory requirements.Assist with vendor audits and audits conducted by sponsors.As required, contribute as a member of the investigational team for CAPAs.Coordinate preparation, review and issue of Standard Operating Procedures (SOPs) to support and maintain Avance Clinical's quality systems.Maintain an up-to-date knowledge of the latest requirements relating to GCP and regulatory requirements in Australia and overseas.Qualifications, Skills and ExperienceBachelor's degree in a life science field.Minimum 2 years' experience as a Quality Assurance professional operating in a GCP or GxP environment with ICH-GCP training.Formal audit training or evidence-based internal/study audit training.Intermediate MS Office suite.What next?As a growing business, we're looking for likeminded people to join us – we hope that's you.To join our team please submit your CV & cover letter as one Microsoft Word document.You must have full Australian working rights to be considered.Quality Assurance / QA / GCP / Adelaide / Melbourne / SydneyApply For Job#J-18808-Ljbffr


Nominal Salary: To be agreed

Source: Talent2_Ppc

Job Function:

Requirements

Site Quality Supervisor (M/F/D) - Night Shift

About the Voith Group The Voith Group is a global technology company. With its broad portfolio of systems, products, services and digital applications, Voith...


Voith Group - New South Wales

Published 13 days ago

Auditor

Flexible working policies including WFH options.Work with a globally recognised Audit brand that values your work/life balance.9-Day working Fortnight and Ti...


Crowe - New South Wales

Published 13 days ago

Technical And Quality Specialist

Are you ready to bring a little extraordinary into your life? At Nespresso, we blend vibrant people and products together to create careers that elevate coff...


Nestlé Sa - New South Wales

Published 13 days ago

Quality Assurance / It Tester

FinXL IT Professional Services is an innovative Australian owned company providing our clients with technology enabled business solutions and consulting serv...


Finxl - New South Wales

Published 13 days ago

Built at: 2024-12-22T01:56:49.254Z