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AstraZeneca

Global pharmaceutical company developing prescription medicines

Labeling Strategy Associate Director

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeMississauga, ON, Canada

About the Job

Requirements

  • A university degree in Science or a related discipline is required.
  • Three to five years of pharmaceutical experience, including regulatory experience, preferably working with labelling, is required.
  • Knowledge of labelling regulations and guidance is required.
  • Strong verbal and written communication skills are required.
  • Attention to detail and accuracy are required.
  • Multicultural awareness and sensitivity, with demonstrated experience communicating and negotiating effectively across diverse cultures, is required.
  • The ability to assimilate clinical and scientific information and present it concisely is required.
  • The ability to think strategically, assess risks appropriately, and formulate risk-management strategies is required.
  • Demonstrated relationship-building skills, including working effectively across formal and informal networks, are required.
  • Negotiation skills, including listening effectively and building consensus, are required.
  • Critical information-seeking skills are required.
  • Rational persuasion skills, including distilling issues to key components and proposing solutions, are required.
  • Interpersonal awareness, including understanding how one's actions affect others, is required.

Responsibilities

  • Ensure that the labelling process is followed throughout the product lifecycle.
  • Ensure all work is performed in accordance with established procedures, regulatory requirements, and GxPs.
  • Lead the development of labelling strategy in line with the product's overall regulatory strategy by interpreting regulations, guidance, and competitor analyses, and anticipating and communicating broader impacts and long-term consequences for the product and portfolio.
  • Lead the Product Labelling Team in preparing and maintaining high-quality Core Prescribing Information, EU Quality Review of Documents, US Prescribing Information, and Instructions for Use through Senior Leader approval, with the aim of achieving advantageous labelling.
  • Lead the development of labelling negotiation strategies and anticipate health authority perspectives.
  • Provide labelling expertise to the Global Regulatory Submission Team, Global Regulatory Execution Team, and Product Labelling Team regarding language, placement, and regulatory content detail for Core Product Information and Market Product Information, in line with company procedures and regional regulations and guidance.
  • Clarify applicable labelling requirements and expectations in complex situations for relevant collaborators, including providing risk insight and proposing mitigations.
  • Evaluate, interpret, and communicate global regulations and trends on labelling and their potential business impacts on product labelling.
  • Ensure appropriate communication across labelling subfunctions.
  • Justify and communicate the labelling rationale to Senior Leaders to enable effective decision-making.
  • Lead the development of target labelling documents as appropriate.
  • Assist in developing labelling policies, procedures, and standard operating procedures.

Desired Qualifications

  • Experience in labelling development and/or maintenance is desirable.
  • Knowledge of labelling regulations in major markets is desirable.
  • Advanced academic training, including a PharmD or PhD, is highly desirable.

About the Company

AstraZeneca

Global pharmaceutical company developing prescription medicines

AstraZeneca develops and markets prescription medicines and vaccines worldwide, with a focus on oncology, cardiovascular/metabolic, respiratory, and infectious diseases. Its products work by targeting specific biological pathways or cells, using small-molecule therapies, biologics, and vaccines to treat diseases or prevent infections. It differentiates itself through its dual heritage from Sweden and the UK, a broad pipeline, and strong R&D and collaborations that move from discovery to patient access. Its goal is to improve people’s health by discovering, developing, and delivering medicines and vaccines to patients worldwide.

Company size
10,001+
Company stage
IPO
Headquarters
Cambridge, United Kingdom
Founded
1913

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