hirly

CSL

Senior Validation Specialist

APAC, AU, Tullamarine, Seqirus

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at CSL first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included

Matched against 2.4M live jobs from 200,000+ employers in 200+ countries.

Tailor my resume for this job →

Apply from your AI assistant

Connect hirly to Claude and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending. ChatGPT: manual setup today.

Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.

hirly's read of this role

Seniority
Senior
Country
AU
Work mode
On-site / unstated
First seen by hirly
9 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

The Opportunity

CSL Seqirus is a global leader in influenza prevention and pandemic preparedness.

We are seeking a Senior Validation Specialist to join our team at our state of the art, manufacturing facility at 2 Sky Rd, Melbourne Airport VIC 3045.

Description of the Role

The Senior Validation Specialist will provide initial qualification (including determining requirements for qualification), re-evaluation and re-qualification support for the design, start-up, commissioning and qualification of equipment (including associated computer systems, facilities, and utilities) and processes. You will own and manage validation deliverables across the site cool rooms and cleanrooms.

This position will primarily work across our Flu Cell Culture (FCC) area which include FCC vaccines (FCC facility) at Seqirus. You will also support work at our Woodend site or PNS facility (Tullamarine), although primarily, you will be working based at and working at Tullamarine.

This is a Permanent full-time position.

Responsibilities:

Act as SME supporting Validation Manager to define validation scope, schedules, and resourcing

Own, manage, and execute validation deliverables and programmes within assigned area

Document and complete validation activities as directed

Build strong, candid relationships within Validation and cross‑functional teams

Influence coordinators and managers to align with validation priorities

Collaborate closely with Manufacturing, QC, Sterility Assurance, MS&T, AS&T, Warehouse, Engineering, Automation, and QA

Lead analysis and resolution of complex validation issues and major deviation investigations

Drive validation assessments for departmental and cross‑functional deviations

Identify and lead validation process improvements and key projects

Support delegation of responsibilities between Validation Specialist and Validation Manager as required

Travel up to 10% as needed

Skills and Experience:

cGMP background in Biological or Pharmaceutical Industry.

Experience in Biological or Pharmaceutical Industry

Bachelor’s degree is required in engineering, technical or science related field.

Good understanding of QMS and Risk Management

Leadership skills supporting team members and leading activities

Time management skills for the execution and planning of work.

Good communication skills both written and verbal, with excellent technical writing skills

Ability to multitask and work cross functionally

This role requires a strong understanding of the process of commissioning, qualification and validation. It is required that this experience is gained through practical experience within a validation function, with evidence of experience across multiple validation competencies. The level of experience required may typically be found through 6+ years of biological or pharmaceutical manufacturing experience, or through equivalent applicable roles. Validation experience within Pharmaceuticals, and demonstrated knowledge of cGMPs, EU and FDA regulatory guidelines, and validation principles required.

Application Period: Applications open on 4 September 2026 and close on 4 October 2026.

About CSL Seqirus

CSL Seqirus is part of 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. With state-of-the-art production facilities in the U.S., the U.K. and Australia, CSL Seqirus utilizes egg, cell and adjuvant technologies to offer a broad portfolio of differentiated influenza vaccines in more than 20 countries around the world.

To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/ .

Our Benefits

For more information on CSL benefits visit How CSL Supports Your Well-being | CSL .

You Belong at CSL

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging

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 visit https://www.csl.com/accessibility-statement .

Watch our ‘On the Front Line’ video to learn more about CSL Seqirus

Original posting on CSL's site ↗

Browse similar roles

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job