Senior Associate - Operational Services at CSL
Melbourne VIC 3000, , Australia -
Full Time


Start Date

Immediate

Expiry Date

07 Nov, 25

Salary

0.0

Posted On

08 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Manufacturing, Regulatory Requirements, Regulated Industry, Biotechnology

Industry

Information Technology/IT

Description

Your Opportunity
Are you passionate about making a difference in the lives of patients worldwide? At CSL Behring, we are driven by our promise to save lives and protect the health of people around the world. We are currently seeking a Senior Associate, Operational Services to join our team with the Base Fractionation Facility (Facility F) at our Broadmeadows site. You will manage the implementation of routine changes in response to manufacturing value stream priorities and provide expertise in the facilitation and analysis of deviation investigations within manufacturing.
This position will be a 2-year fixed term contract.
Your Role

Reporting to the Manager, Operational Services Facility F, your responsibilities will include:

  • Investigate manufacturing deviations, lead investigation teams, and manage documentation.
  • Collaborate with Quality Assurance and manufacturing teams to assess risks and communicate findings.
  • Represent manufacturing value stream as change coordinator for BMW portfolio and engineering projects.
  • Drive cross-functional task completion for routine changes to existing and new processes.
  • Engage the right subject matter experts (SMEs) to ensure effective change implementation.
  • Plan and coordinate changes, ensuring timely progress and stakeholder alignment.

Your Experience

  • Tertiary Qualification in Science or Engineering.
  • Demonstrated manufacturing experience (R&D, Tech Services, Quality or Manufacturing) in a pharmaceutical, biotechnology, biological or a regulated industry.
  • Basic to intermediate project and change management experience, working as part of a larger team.
  • Strong understanding of cGMP, regulatory requirements and relevant environmental, health and safety requirements as applicable to secondary manufacturing.

Apply now for a role now with a varied remit in an organisation going through considerable investment and change.
Please submit your application including your CV in one document.

LI-Onsite

Responsibilities
  • Investigate manufacturing deviations, lead investigation teams, and manage documentation.
  • Collaborate with Quality Assurance and manufacturing teams to assess risks and communicate findings.
  • Represent manufacturing value stream as change coordinator for BMW portfolio and engineering projects.
  • Drive cross-functional task completion for routine changes to existing and new processes.
  • Engage the right subject matter experts (SMEs) to ensure effective change implementation.
  • Plan and coordinate changes, ensuring timely progress and stakeholder alignment
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