Senior Manager, Core Labeling Strategy

1100 Mylan Pharmaceuticals Inc.; Washington (District of Columbia); On-site; USD 95,000 - 193,000; Full time

Benefits offered by this job

Competitive salary

Benefits

Inclusive environment

Job summary

Viatris is seeking a Senior Manager, Core Labeling Strategy to lead global and territorial labelling initiatives. The role requires coordinating with Regulatory, Medical, Safety and Clinical teams to ensure accurate, compliant labelling across products and markets.

The candidate will guide development of core labelling (CCDS, TPL) and support responses to Health Authority requests, while coordinating with cross-functional partners to maintain alignment with corporate goals.

Qualifications

• Bachelor’s degree in Science, Medicine, Pharmacy or related field.
• 7–10 years of labelling experience, including global core labelling development.
• Experience supporting regulatory submissions (NDA/BLA/MAA) preferred.
• Strong interpersonal and communication skills.
• Ability to influence effectively in a cross-functional team environment.

Responsibilities

• Accountable for management and delivery of labelling activities across assigned products/portfolio.
• Leads development, preparation, review, and approval of global labelling documents (e.g. TPL, CCDS, Core Patient Information) and territorial labelling (e.g. EU SmPC, USPI).
• Leads or supports development of labelling strategy in partnership with Global Regulatory, ensuring alignment with strategy and business objectives.
• Establishes cross-functional partnerships with Regulatory, Medical, Safety, and Clinical teams for labelling development.

Skills

Labelling expertise

Regulatory strategy

Cross-functional collaboration

Stakeholder management

Scientific writing

Presentation skills

Supervisory experience

Education

Bachelor's degree in Science/Medicine/Pharmacy

Advanced degree advantageous

Job description

Mylan Inc. Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases. We have been included on number of award lists that demonstrate the impact we are making. Every day, we rise to the challenge to make a difference and here's how the Senior Manager, Core Labeling Strategy will make an impact:

Key responsibilities for this role include:

• Accountable for management and delivery of labelling activities across assigned products/portfolio.
• Leads development, preparation, review, and approval of global labelling documentation (e.g. TPL, CCDS, Core Patient Information) and territorial labelling (e.g. EU SmPC, USPI) based on clinical and non-clinical data.
• Leads or supports development of labelling strategy in partnership with Global Regulatory, ensuring alignment with overall regulatory strategy and business objectives.
• Contributes to development and maintenance of Target Product Labelling (TPL) to support early development, regulatory positioning, and cross-functional alignment.
• Establishes strong cross-functional partnerships with Regulatory Strategists, Medical, Safety, and Clinical teams to ensure proactive and effective labelling development.
• Leads labelling updates and development, critically evaluating supporting data to ensure scientific accuracy, clinical relevance, and regulatory acceptability.
• Assesses and reconciles deviations from Company Core Position (e.g. CCDS) and supports responses to Health Authority requests.
• Chairs or actively contributes to Product Labelling Teams (PLTs), ensuring appropriate cross-functional input.
• Escalates key issues to the Global Labelling Committee (GLC) as required.
• Maintains strong awareness of competitor labelling, evolving regulatory requirements, and external trends to inform labelling strategy.
• Manages complex regulatory and scientific labelling issues, balancing compliance, business needs, and risk.
• Contributes to interpretation and application of emerging regulatory guidelines impacting labelling.
• May represent Viatris in external forums (e.g. industry groups, EMA/FDA workshops).
• Reviews and approves promotional and non-promotional materials for alignment with CCDS and applicable codes and requirements.
• Reviews and advises on key scientific and regulatory documents (e.g. IB, protocols, CSR, PSURs, RMPs) as appropriate.
• Provides labelling expertise in cross-functional and regulatory team discussions.
• Performs other labelling-related duties as assigned.

The minimum qualifications for this role are:

• Bachelor’s degree (or equivalent) in Science, Medicine, Pharmacy, or related field with typically 7-10 years of experience, including significant labelling experience.
• Demonstrated experience in development and maintenance of global core labelling (e.g. CCDS) and major market labelling (e.g. USPI, EU SmPC).
• Experience supporting regulatory submissions (e.g. NDA/BLA/MAA) preferred.
• Advanced degree (MSc, PharmD, PhD) is advantageous but not required.
• Experience in TPL development, competitive labelling benchmarking, and regulatory strategy support is an advantage.
• Highly developed interpersonal, presentation and communication skills.
• Ability to provide innovative approaches/recommendations to product labelling that meet corporate goals while maintaining compliance with relevant laws and regulations.
• The ability to influence effectively in a matrixed, cross-functional team environment Position functions autonomously.
• The position may directly supervise employees. Carry out supervisory responsibilities in accordance with the organization's policies and applicable laws. Responsibilities may include interviewing, hiring, and training employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems.

Exact compensation may vary based on skills, experience, and location.

The salary range for this position is $95,000 - $193,000.

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.

Viatris is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, gender expression, disability, or protected veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations.

Viatris is a global healthcare company formed in 2020 through the combination of Mylan and Upjohn, a legacy division of Pfizer. By integrating the strengths of these two companies, including our global workforce, we aim to deliver increased access to affordable, quality medicines for patients worldwide, regardless of geography or circumstance. We believe in healthcare as it should be - empowering people worldwide to live healthier at every stage of life. Because of our unwavering belief that better access leads to better health, we leverage our best-in-class manufacturing and scientific expertise and proven commercial capabilities to bring quality medicines to patients when and where they need them.