Head of Global Labelling

Head of Global Labelling

The Role

CSL Seqirus influenza vaccine portfolio reaches millions of people every year and every one of those products depends on labelling thats scientifically sound regulatory compliant and is clear and informative for the end-user. This role leads the function responsible for labelling globally with a seat on the regulatory leadership team and as Chair of the Global Labelling Committee.

As Head of Global Labelling youll shape the strategic direction of labelling for Seqirus worldwide portfolio reporting to the VP Regulatory Affairs & Pharmacovigilance. Its the point where clinicaldata regulatory requirement and commercial reality converge to ultimately define how a product is understood and used.

What Youll Be Responsible For

Youll lead a global team of established labelling professionals coaching them in strategic thinking and the leadership behaviours Seqirus expects of its people while owning the end-to-end labelling review and approval process and driving its continuous improvement.

Youll set global labelling strategy balancing business need against the core obligation of getting benefit/risk information right for the people relying on it and youll ensure the underlying processes deliver accurate timely labelling information that supports the safe and effective use of Seqirus products importantly including the regulatory requirements around timely safety-related updates.

Separately youll ensure efficient labelling operations support for the time-critical annual strain updates that seasonal influenza vaccines require.

Beyond the team youll provide labelling perspective to governance bodies represent Seqirus position in external regulatory forums and provide labelling subject matter expertise for internal and external labelling-related audits. Youll work closely with cross-functional stakeholders including Global Safety Clinical Development Commercial and Supply Chain to ensure effective and timelylabelling deliverables meet business needs across every region Seqirus operates in.

Experience Required

• Significant experience in Global Regulatory Affairs with a strong focus on product labelling and management of core labelling documentation.
• Proven leadership of global multi-country teams including coaching and developing talent.
• Track record owning and continuously improving a regulated process end-to-end.
• Experience representing a companys positions to governance bodies or external regulators.
• Working familiarity with labelling-related audits and the regulatory frameworks that govern labelling compliance.
• Director-level experience (or equivalent) in a global pharma or biotech organization.

About CSL Seqirus

CSL Seqirus is part ofCSL. As one of the largest influenza vaccine providers in the world CSL Seqirusis 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.

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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.

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

Required Experience:

Director

Employment Type : Full-Time
Experience: years
Vacancy: 1