Head of Global Labelling

CSL Plasma Inc.

New York (NY)

On-site

USD 150,000 - 200,000

Full time

14 days+
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Benefits offered by this job

Health benefits
Diversity and inclusion initiatives
Flexible work options

Job summary

CSL Plasma Inc. is looking for a Head of Global Labelling to lead the strategic direction for labelling across Seqirus’ influenza vaccine portfolio. You will ensure that all labelling is scientifically sound and compliant with regulations while coaching a global team of labelling professionals.

This role requires significant experience in Global Regulatory Affairs and leadership in a global pharma environment. The ideal candidate will enhance labelling processes to improve product safety and compliance globally.

Qualifications

  • Significant experience in Global Regulatory Affairs focused on product labelling.
  • Proven leadership of global, multi-country teams.
  • Track record in managing and improving regulated processes end-to-end.

Responsibilities

  • Lead a global team in strategic labelling.
  • Set global labelling strategy and ensure compliance.
  • Represent Seqirus in external regulatory forums.

Skills

Global Regulatory Affairs
Product labelling
Leadership in multi-country teams
Regulated process improvement
Labelling-related audits

Education

Director-level experience in pharma or biotech

Job description

## Head of Global Labeling応募locations: Seqirus UK - Maidenhead: Seqirus Netherlands - Amsterdam: APAC, AU, Victoria, Melbourne, CSL Limited Melbourne: Seqirus USA - MA - Walthamtime type: 正社員posted on: 募集開始 - 今日job requisition id: R-280666**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 that's 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, you'll shape the strategic direction of labelling for Seqirus’ worldwide portfolio, reporting to the VP Regulatory Affairs & Pharmacovigilance. It's the point where clinical data, regulatory requirement, and commercial reality converge to ultimately define how a product is understood and used.**What You'll Be Responsible For**You'll 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.You'll set global labelling strategy, balancing business need against the core obligation of getting benefit/risk information right for the people relying on it, and you'll 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, you'll ensure efficient labelling operations support for the time-critical annual strain updates that seasonal influenza vaccines require.Beyond the team, you'll 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. You'll work closely with cross-functional stakeholders including Global Safety, Clinical Development, Commercial and Supply Chain to ensure effective and timely labelling 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 company's 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 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**### Equal Opportunity EmployerCSL 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 click here.
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