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Validation Specialist

Last update 2024-04-18
Expires 2024-04-17
ID #2101203691
Free
Validation Specialist
Australia, Western Australia, Perth,
Modified April 4, 2024

Description

We are looking for a Validation Specialistto join the Analytical Sciences and Technology (AS&T)team in Parkville Australia.

In this interesting, fixed term role, until30 June 2025 , you will participate in the validation and implementation of scientific methods and technologies into the Quality Control laboratories.

The Role Reporting to the Senior Manager Site Analytical Services & Technology and working on site, you will: Support the implementation of projects and ensuring training requirements.

Participate in routine internal audits, ensuring all audit items are closed out as per agreed timeline.

Participate and perform in document write up and review for Regulatory submissions.

Collaborate with QC, Production, QA, Document Control, and all R&D groups to implement selected technologies into the QC laboratories.

Collaborate with external colleagues and companies to maintain knowledge of current assay developments and current scientific technology.

Participate in Assay Development Teams including creating required documentation, conducting assessment testing and ensuring milestones are met for development and transfer with efficient use of labour and material resources.

Create required documentation as outlined in relevant procedure for testing and standard operating procedures for implementing new methods and technologies.

Conduct analyst training within AS&T and QC Laboratories for transferred technologies.

Maintain associated databases of relevant information to AS&T and support project monitoring systems.

Your skills and experience To be considered for this role you have: A Bachelor of Science or equivalent Previous laboratory testing experience with experience in biochemistry and/or chemistry techniques Experience in the pharmaceutical industry Good technical and mechanical aptitude Understanding of the process for the development and validation of analytical test methods.

Understanding of the ICH/EMEA guidelines and Pharmaceutical Regulatory Requirements Previous experience in project management How to apply Please send us your resume and covering letter (in one document), which addresses the criteria above and includes the reference number R-227908by7 April, 2024.

#LI-Onsite CSL Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives.

Learn more about some of the benefitsyou can participate in when you join CSL Seqirus.

About CSL Seqirus CSL Seqirus is part of CSL Limited (ASX: CSL).

As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness.

In Australia, CSL Seqirus is also a leading provider of speciality pharmaceuticals and other essential vaccines.

Learn more about CSL Seqirus.

We want CSL Seqirus to reflect the world around us As a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion.

Learn more about Diversity & Inclusionat CSL Seqirus.

Do work that matters at CSL Seqirus!Watch our 'On the Front Line' video to learn more about CSL Seqirus Equal Opportunity Employer CSL is an Equal Opportunity Employer.

If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please clickhere.#J-18808-Ljbffr

Job details:

Job type: Full time
Contract type: Permanent
Salary type: Monthly
Occupation: Validation specialist

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