Validation Specialist - Global Pharma (Contract, Melbourne)

Bell People Consultants; Melbourne; Vor Ort; AUD 90.000 - 120.000; Vollzeit

Benefits dieser Stelle

Contract role

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Zusammenfassung

Bell People Consultants in Melbourne seeks a Validation Associate to support a leading global pharmaceutical manufacturer’s validation group. You will plan and execute qualification activities, ensuring compliance, quality, and timely delivery across multiple projects.

The ideal candidate holds a Science or Engineering degree with 3–5 years in validation, including cleaning and water sampling validation, and experience with KN EAT/validation software.

Qualifikationen

• 3–5 years of validation experience required.
• Experience with cleaning, process and water sampling validation.
• Proficient in MS Office and validation software (e.g., KNEAT).

Aufgaben

• Prepare & execution of validation protocols.
• Execute cleaning validation and/or water sampling validation.
• Participate in QC equipment & manufacturing validation.
• Close out validation protocols & troubleshoot & resolve issues.
• Create documentation & execute validation for complex projects.
• Liaise with QC/QA, Engineers & Validation Teams.

Kenntnisse

Validation experience

Water sampling

Process validation

Ausbildung

Science or Engineering degree

Tools

KNEAT

MS Office

Jobbeschreibung

Operating as a global pharmaceutical manufacturer, our client is well known for its growth and innovation offering a range of healthcare and pharmaceutical products to local & global markets.

Due to increase in project requirements, an opportunity has now arisen for a ManufacturingQA Associateto provide QA support in deviations, change controls & CAPA's across manufacturing, engineering & quality.

About the Opportunity:

Reporting to the Quality Manager, key duties include the following:

• Lead investigations & write up deviations, complete & write CAPA's & change controls to regulatory guidelines.
• Review quality documents, change controls & quality compliance work.
• Provide & represent QA in GMP manufacturing operations.
• Work with manufacturing teams to ensure improvements in compliance for CAPA's.
• Work collaboratively across functions in quality, engineering & manufacturing to ensure metrics are met.
• Effectively liaise with internal & external key stakeholders.

About You:The successful candidate will have the following skills & experience:

• Tertiary qualifications inScience or Engineering.
• Sound experience in Pharmaceutical/Medical Device Manufacturing or highly regulated environment.
• Sound knowledge of QA, CAPA's & deviations within manufacturing.
• Strong GMP knowledge.
• Excellent Attention to detail & strong organisational skills.
• Ability to work with wide range of stakeholders.

Culture & Benefits:

This is an ExcellentContract Opportunityfor a ManufacturingQA Associateto join a leading global pharmaceutical organisation to support manufacturing operations, drive change controls & deviations for a major project.

How To Apply

To Apply for this role, please click the APPLY NOW button.

For a confidential discussion, please contact Sue Campbell on 0417 994 ***.
NB - Only Shortlisted candidates will be contacted.

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