Senior Associate, Quality Assurance & Regulatory Affairs

Healthcare Professionals Group · Sydney NSW 2000 · Part time
Posted 11d ago

Senior Associate, Quality Assurance & Regulatory Affairs

Healthcare Professionals Group
Sydney NSW 2000

·

Part time

~$80k - $100k(Estimated)
Competitive salary + company benefits
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KEY POINTS WE FOUND
  • Permanent opportunity within an international pharmaceutical company
  • Broad role across both Regulatory Affairs and Quality Assurance
  • Work closely with local, regional and global stakeholders

Benefits

  • Permanent opportunity within an international pharmaceutical company
  • Broad role across both Regulatory Affairs and Quality Assurance
  • Work closely with local, regional and global stakeholders

About the company
A global pharmaceutical organisation with an established Australian presence and a strong commitment to quality, compliance and patient outcomes.
About the opportunity
An exciting opportunity has become available for a Senior Associate, Quality Assurance & Regulatory Affairs to join an international pharmaceutical organisation. This is a broad, hands-on position covering both Regulatory Affairs and Quality Assurance.
You will support regulatory submissions and lifecycle activities across Australia and New Zealand, while also contributing to the ongoing management of the Quality Management System, GMP compliance and broader quality activities.
This would suit someone with established pharmaceutical RA and/or QA experience who enjoys working across both functions and is looking for broader responsibility and exposure.

Duties

  • Prepare, submit and manage regulatory applications to the TGA and Medsafe
  • Support regulatory activities throughout pre-submission, submission and evaluation
  • Coordinate responses to Health Authority questions and requests
  • Maintain regulatory dossiers, submission records and product-specific documentation
  • Support ARTG applications, variations, renewals and ongoing product lifecycle activities
  • Review Product Information, labels, artwork, packaging and related materials for compliance
  • Assess regulatory impact of manufacturing, supplier, formulation, packaging and testing changes
  • Support TGA GMP clearances, including applications, renewals and supporting documentation
  • Maintain and support Quality Management System activities including deviations, CAPAs, change controls and complaints
  • Support supplier qualification, vendor compliance and quality agreements
  • Assist with product quality reviews, recalls, investigations and batch release activities
  • Support audit, inspection and compliance readiness

Skills and Experience

  • Tertiary qualification in Pharmacy, Pharmaceutical Sciences, Life Sciences, Biotechnology, Chemistry, Microbiology or a related discipline
  • 3 to 5 years' experience within pharmaceutical Regulatory Affairs or Quality Assurance
  • Experience supporting or managing regulatory submissions
  • Knowledge of TGA regulatory requirements, with Medsafe exposure highly regarded
  • Good understanding of GMP requirements and pharmaceutical quality systems
  • Experience across QMS activities such as deviations, CAPAs, change controls or complaints advantageous
  • Experience within a pharmaceutical sponsor, manufacturer or distribution environment highly regarded
  • Strong attention to detail and documentation skills
  • Strong organisation and time management skills with the ability to manage competing priorities
  • Excellent communication and stakeholder management skills
  • Ability to work independently while collaborating effectively across teams

Culture
Join a collaborative and quality-focused environment where you will work across multiple areas of the business and have the opportunity to broaden your Regulatory Affairs and Quality Assurance experience.
How to Apply
Ready to take the next step? Click apply or contact Gemma Staddon on gstaddon@hpgconnect.com for a confidential discussion.
About Healthcare Professionals Group
Healthcare Professionals Group recruits all positions: executive, permanent, contracting/temp, at all levels, across all areas of healthcare - Pharmaceuticals, Biotechnology, Medical Technology and Clinical Care.

  • Medical Affairs & Life Sciences Recruitment - Clinical Research, Market Access, Medical Affairs, Pharmacovigilance, Quality, Data Management, Regulatory Affairs, Scientific;
  • Commercial Recruitment - Marketing, Sales, Analytics, Government and External Affairs;
  • Business Operations & Infrastructure Recruitment - Administration, Customer Service, Engineering, Finance, Human Resources, IT, L&D, Legal, Manufacturing, Operations, Supply Chain, Warehouse;
  • Clinical Care Recruitment - Allied Health, Aged Care, General Practice, Medical Imaging, Medical Management, Medical Specialties, Nursing.
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Skills

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Attention to detailDocumentation skillsGmp compliancePharmaceutical quality systemsQuality management systemRegulatory affairsRegulatory submissionsStakeholder managementTime management

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Senior Associate, Quality Assurance & Regulatory Affairs | Healthcare Professionals Group | Australian Ageing Agenda