Senior Associate Operational Services, Filling at CSL

Melbourne, Victoria, Australia -

Full Time

Start Date

Immediate

Expiry Date

01 May, 26

Salary

0.0

Posted On

31 Jan, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Continuous Improvement, Project Management, Change Management, Data Analysis, Root Cause Investigation, cGMP, Regulatory Requirements, Manufacturing Experience, Process Optimization, Team Leadership, Validation Technology, Pharmaceutical Industry Knowledge, Environmental Health, Safety Requirements, Criticality Assessment, Process Capability Changes

Industry

Pharmaceutical Manufacturing

Description

Your Opportunity At CSL Behring, we are driven by our promise to save lives and protect the health of people around the world. We are committed to fostering a diverse, inclusive, and collaborative workplace where every team member feels valued and empowered to make a difference. We are currently recruiting for a Senior Associate Operational Services, Filling to join our team at Broadmeadows site. Reporting to the Manager Operational Services Filling, you will play a crucial role in managing continuous improvement initiatives and driving implementation of changes aligned with manufacturing value stream priorities. NOTE - There are two 12-month fixed term contract positions (project based). Your Role Lead continuous improvement projects, ensuring prioritisation and allocation of resources is aligned with value stream priorities. Lead a cross functional team in the implementation of short- and long-term process optimisation, correction or process capability changes. Representing the manufacturing value stream as change coordinator on teams operating to implement BMW portfolio projects and engineering projects. Monitor change and investigations for completion to plan and escalate to ensure implementation is timely and effective. Monitor process performance and reliability through effective data analysis and utilising appropriate tools to communicate to the broader team. Investigator for deviations at all levels of criticality from within the manufacturing area. Maintain expertise in change management, project management, root cause investigation and facilitation through ongoing formal training and review and analysis. Your Skills and Experience Tertiary Qualification in Sciences or Engineering. Demonstrated manufacturing experience (R&D, Tech Services, Quality or Manufacturing) in a pharmaceutical, biotechnology, or biological industry. Experience in project and change management particularly in leading change. Knowledge of validation technology, production and management processes within and external to the pharmaceutical industry. Proven understanding of cGMP, regulatory requirements and relevant environmental, health and safety requirements as applicable to secondary manufacturing. Ability to work on complex tasks. How to Apply Please submit your application in one document including your resume. Apply now to join CSL Behring and help us deliver on our promise to patients! #LI-Onsite

Responsibilities

Lead continuous improvement projects and manage the implementation of changes aligned with manufacturing value stream priorities. Monitor process performance and reliability while representing the manufacturing value stream in various projects.