About the Company
Operating as a major global Multinational pharmaceutical manufacturer with global sites worldwide, our client is well known for its growth and innovation and is an Australian iconic brand in the marketplace,
An opportunity now exists for a
Quality &Validation; Specialist with a Microbiology/Biochemistry
experience to lead, coordinate cross site activities for method development activities within a cGMP workplace.
About the Position
Key Duties & Responsibilitiesinclude the following:
Lead troubleshooting issues within QC methods to deliver solutions for implementations through quality systems. (CAPA, Change control)
Act as a SME for execution of method standardisation & robustness program.
Responsible for experimental design on key projects and deliverables.
Review data generated from validation activities and observe data trends on key projects that involve new technologies & processes.
Development of current and new test methods validation lifecycle.




Effectively liaise with key internal and external stakeholders.
About You
Tertiary Qualifications in Science.
Sound Microbiology/biochemistry background is essential.
Sound Industry experience in pharmaceutical, medical device industries.
Method validation andvalidation procedures and documentation.
Good understanding of cGMP practices & industry guidelines.
Sound communication & interpersonal skills.
Excellent attention to detail.
This is an Excellent Long Term Contract Opportunity for
Quality &Validation; Specialist
with Method Validation and a Microbiology or Biochemistry background
to further develop skills and experience within a large global pharmaceutical organisation.
This contract opportunity requires Immediate Start ASAP.
Global Pharmaceutical Manufacturer
Excellent Contract Opportunity - Start ASAP
Melbourne Metropolitan Area
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📌 Quality & Validation Specialist (Melbourne)
🏢 Bell People Consultants
📍 Melbourne