Job Description
About the Company
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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,
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An opportunity now exists for a Quality &Validation; Specialist with a
Microbiology/Biochemistryexperience
to lead, coordinate cross site activities for method development activities within a cGMP workplace.
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About the Position
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Key Duties &
Responsibilitiesinclude
the following:
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Lead troubleshooting issues within QC methods to deliver solutions for implementations through quality systems. (CAPA, Change control)
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Act as a SME for execution of method standardisation & robustness program.
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Responsible for experimental design on key projects and deliverables.
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Review data generated from validation activities and observe data trends on key projects that involve new technologies & processes.
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Development of current and new test methods validation lifecycle.
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Effectively liaise with key internal and external stakeholders.
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About You
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Tertiary Qualifications in Science.
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Sound
Microbiology/biochemistry
background is essential.
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Sound Industry experience in pharmaceutical, medical device industries.
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Method validation andvalidation procedures and documentation.
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Good understanding of cGMP practices & industry guidelines.
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Sound communication & interpersonal skills.
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Excellent attention to detail.
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This is an Excellent Long Term Contract Opportunity for Quality &Validation; Specialistwith Method Validation and a Microbiology or Biochemistry backgroundto further develop skills and experience within a large global pharmaceutical organisation.
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This contract opportunity requires Immediate Start ASAP.
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Global Pharmaceutical Manufacturer
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Excellent Contract Opportunity - Start ASAP
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Melbourne Metropolitan Area
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#J-*****-Ljbffr

📌 Quality & Validation Specialist (Victoria)
🏢 Bell People Consultants
📍 Victoria