Closing Date:
28/02/2013
Requisition Number
6697
Location: Parkville, Victoria,
Australia
Category: Quality
Job Type: Temporary
Duties:
CSL Limited is a company that fosters a work culture
emphasizing Superior Performance, Innovation, Integrity, Collaboration and
Customer Focus with a commitment to support, train and grow its people. An
outstanding opportunity is available for a Senior Associate to join the Quality
group at bioCSL to be responsible for reviewing release documentation to ensure
schedules are met. Reporting to the Manager – QA Release, your responsibilities
will include:
• Coordinate and
review the relevant product portfolio batch / release documentation
• Liaise with DCI
group to ensure that deviations and change controls are managed
• Supervise and train
Associates performing batch release processes
• Assist the DCI
group in investigating adverse events and PTCs as required
• Prepare and review
summary protocols for regulatory requirements / customers
Qualifications:
To be successful in this role you will possess; a minimum
tertiary qualification and experience in pharmaceutical manufacturing; strong
analytical skills and knowledge of GxP, domestic and international regulations;
sound knowledge of manufacturing processes and registered conditions,
demonstrated ability for conceptual and analytical thinking with good judgement
to reconcile ambiguities, and the ability to develop and supervise direct
reports. This is a 12 month fixed term (maternity leave replacement) position.
Applications close AEST 4pm Thursday 28 February 2013
How to Apply:
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