REGULATORY SCIENCES MANAGER

Why Patients Need You We're looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity.
Adhering to local and global regulations is essential and the ever-changing regulatory environment requires forward thinking and attention to detail.
Your dedication and expertise will help expand and accelerate patient access to Pfizer medicines and vaccines.
What You Will Achieve You will represent Pfizer as an Approval Liaison in the regulatory affairs team.
You will play the critical role of providing strategic product direction to teams while interacting with regulatory agencies and negotiating with them to expedite approval of pending registrations.
Due to your expertise, you will be the Regulatory Liaison on the project team throughout the product lifecycle and a regulatory representative to marketing or research project teams and government regulatory agencies.
Your understanding of regulatory procedures will help in development of submission of product registration, progress reports, supplements, amendments, and periodic experience reports.
As a Manager, your breadth of knowledge on internal or external business challenges will help us improve our products, processes and services.
Your will guide us to lead projects by meeting objectives and preparing forecasts for resource requirements.
Your risk-taking ability will help us advance new concepts and methodologies.
You will provide technical guidance and oversight to team members and help in problem solving.
It is your hard work and commitment that will make Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It Manage multiple projects/ ongoing work activities within the department typically involving cross-functional representatives.
Provides technical, functional guidance and oversight to team members within the department.
Ensure that quality standards are met and that the deliverables meet strict deadlines and fulfil local regulatory standards.
Ensure local licenses under country responsibility are maintained in compliance with local regulations and following corporate policies, regulatory processes, and Standard Operating Procedures (SOP).
Work with Global Product Owners and cross functional team to ensure preparation and submission of Global Annual Reports (AR) for NDAs & ANDAs(Abbreviated New Drug Application).
Act as the Regulatory Lead for Life Cycle management (LCM) and work with regulatory strategist and cross functional teams to ensure preparation of quality global regulatory strategy document and supplements/variations.
Update the assigned local product documents in consistency with the local regulations and in the related systems.
Manage and oversee all relevant maintenance activities potentially including Life Cycle management strategy.
Identify and assesses regulatory risks associated with assigned projects and timely communication to the leadership team to quickly mitigate the risks.
Drive resolution of identified issues by communicating issue, impact and outcomes to global regulatory management and core team.
Negotiate with and influences management, cross functional teams and colleagues  to ensure project timelines and quality expectations are met.
Manage the budget and resources allocated to the Regulatory Teams.
Set objectives and manage team performance to achieve best outcomes for business, ensure right training and upskill plans for team.
Qualifications Must-Have Bachelor's Degree (BA/BS) and 5+ years of experience.
Demonstrated ability to apply regulatory guidelines/regulations to successful dossier preparation, submission, and maintenance.
Strong analytical skill and technical/ scientific competence.
Good oral and written communication skills.
Analytical problem solving skills.
Good decision making skills.
People management experience.
Nice-to-Have Master's degree (MA/MBA/MS) and 3+ years of experience.
Doctorate (PhD/PharmD/JD).
Knowledge pharmaceutical legislation in region.
Good business acumen.
Working knowledge of Local and International Regulatory Guidelines.
Declaración de igualdad de oportunidades Nos comprometemos a garantizar que todas las personas interesadas en trabajar en Pfizer sean tratadas por igual, sin discriminación por motivos de género, reasignación de género, orientación sexual, estado civil, raza, color, nacionalidad, origen étnico o nacional, religión o creencia, discapacidad o edad.
Regulatory Affairs #LI-PFE Una carrera en Pfizer es como ninguna otra.
En nuestra cultura de propiedad individual, creemos en nuestra capacidad para mejorar el futuro de la sanidad y en nuestro potencial para cambiar millones de vidas.
Estamos buscando talento nuevo para unirse a nuestra comunidad global, para descubrir nuevas terapias innovadoras que hagan del mundo un lugar con mejor salud.