Associate Director, BioNTainer Australia, Technical QA (Melbourne, VIC, AU, VIC 3000)
About this opportunity
Melbourne, Australia | full time | Job ID: 11802
About the Role:
In this exciting position, you will play a pivotal role in establishing and developing the Technical Quality Assurance (QA) organization and processes for our BioNTainer site in Australia (BTR-AUS) Your expertise will ensure GMP compliance and oversee Technical QA activities for manufacturing (MFG) and QC, supporting the site’s implementation, equipment setup, technology transfer, qualification/validation activities, and more You will also help foster a strong Quality mindset within the organization while maintaining compliance with national and international regulations This role offers a unique opportunity to contribute to BioNTech’s mission of pioneering individualized immunotherapies on a global scale
Your Contribution:
Collaborate closely with the local BTR-AUS site, BioNTainer QA organizations (global and other sites), and wider Quality teams to ensure adherence to all relevant regulations and procedures
Establish and develop a fit-for-purpose Technical QA structure for Manufacturing and QC in Australia, driving continuous improvement
Lead, mentor, and manage the Technical QA team(s) while optimizing resource allocation for the site
Support the creation and implementation of GMP standards and procedures tailored to the Technical QA organization at BTR-AUS
Provide technical QA input for key activities such as equipment setup, technology transfer, qualification/validation processes, method/process validation, deviations, investigations, change controls, audits, and inspections
Author GMP-compliant documentation (e.g., SOPs), contribute to regulatory submissions, Annual/PQ Reviews as applicable, and Management Reviews
Develop and manage Quality metrics for the site while supporting Quality Council operations alongside internal (local/global) and external stakeholders
Deliver hands-on leadership by training staff and fostering an interactive team environment
A Good Match:
Bachelor’s degree in a relevant scientific discipline; advanced qualifications (PhD, MSc, MBA) are advantageous
8+ years (Associate Director) or 10+ years (Director) of significant experience in pharmaceutical GMP functions
Expertise in sterile dosage forms, early-phase platforms, RNA/biologics production is advantageous
Familiarity with TGA/PIC/S regulations; knowledge of ICH, US FDA, EMA guidelines is a plus
Experience with regulatory inspections/audits on national or international levels
Strong solution-driven mindset with excellent interpersonal skills
Strong ability to conceptualize complex processes in fast-paced environments while navigating ambiguity
Proven leadership experience managing teams/budgets effectively
Outstanding verbal/written communication skills with an ability to build consensus across cross-functional teams
Willingness to travel
What we do with the BioNTainers:
We want to improve healthcare by making our innovations accessible worldwide. Therefore, we developed the first modular mRNA-manufacturing facilities based on a container solution called “BioNTainers”. Help us build a regional manufacturing network in Africa & Australia: With the region and for the region. As a part of the local team, driving the establishment of the regional end-to-end mRNA manufacturing solutions.
Benefits for you:
BioNTech is committed to the wellbeing of our team members and offers a variety of benefits in support of our diverse employee base. We offer competitive remuneration packages which is determined by the specific role, location of employment and also the selected candidate’s qualifications and experience.
Click here to find out more about what we do, the careers we offer ans also the benefits we provide. Note: The availability, eligibility and design of the listed benefits may vary depending on the location. The final requirements for the individual use of our benefits are based on the company's internal policies and applicable law.
How to apply:
Apply now by sending us your application documents including Curriculum Vitae, copy of ID, copies of degree certificates and professional certificates, motivation letter as well as your contact details via our online form.
Please note:
Only applications sent via our online form shall be considered. By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider ‘HireRight’. You will be informed accordingly by your BioNTech-Recruiter.
We are looking forward receiving your application.
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Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 383 comparable Associate Director Quality roles across 94 biopharma companies.
Salary context
76 of 383 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 383 comparable roles
+ 29 more countries
Seniority mix
383 of 383 peers have a known seniority level
Therapeutic area mix
0 of 383 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
No peers with a known therapeutic area yet.
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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How we calculate "similar"
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Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.