The OpportunityLocated in Parkville (Australia), we are looking for
Senior Validation Associate to join the great team at Parkville (Australia). In this fixed term full-time position, until 30 June 2026, to support the Parkville Site Exit and Decommissioning activities by generating facility decommission plans aligned with the Decomissioning Site Validation Master Plan. You will provide technical expertise on the requirements for final validation activities and help execute end-of-life GMP activities for Parkville.
The RoleReporting to the Manager Validation and managing a small team:
- Generate the facility decommissioning plans and associated reports.
- Assist in planning, co-ordinating and monitoring the revalidation activities in accordance with the Decommissioning Facility Plans.
- Prepare and review, implement and maintain department documentation for re-validation and validation.
- Participate in internal and external audits as requested
- Build and maintain sound collaborative relationships with key stakeholdersActively participate in resolving constraint’s and identifying opportunities for improvements
- Ensure department staff have appropriate cGMP training
- Ensure department staff follow documented procedures to maintain a safe work environment in compliance with CSL polices, procedures and statutory obligations.
- Ensure their own and others health, safety and security at work
- Investigate re-validation failures with key SME’s to determine impact to product quality and appropriate CAPA to address root cause.
Your skills and experienceTo be considered for this role, you have:
- A relevant Science or engineering tertiary qualification and demonstrated experience in a related environment.
- 5+ years experience in the pharmaceutical manufacturing industry
- 3+ years’ experience applying validation principles to processes, cleaning and equipment
- Experience in decommissioning activities
- Experience in a role solving complex problems and collaborating across different departments
- Experience communicating and collaborating with key stakeholders across the organisation to influence outcomes
- Experience in a role with changing priorities and coordinate multiple tasks
How to apply:Please send us your resume and covering letter (in one document), which addresses the criteria above and includes reference number R-232228 by June 8, 2024.#LI-ONSITE
Our BenefitsCSL 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 you can participate in when you join CSL Seqirus.About CSL SeqirusCSL 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 .We want CSL Seqirus to reflect the world around usAs a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about at CSL Seqirus.Do work that matters at CSL Seqirus!Watch our ‘On the Front Line’ video to learn more about CSL Seqirus
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