Labeling Strategist (m/f/x) (Global Labeling Strategy Lead)

JR Germany; Braunschweig; Hybrid; EUR 60.000 - 100.000; Vollzeit

Zusammenfassung

An established industry player is seeking a Regulatory Affairs expert to lead global labeling initiatives. This role involves strategic oversight of product labeling compliance, managing complex projects, and collaborating with cross-functional teams. The ideal candidate will have extensive experience in the pharmaceutical sector, particularly in regulatory affairs and labeling. This position offers the flexibility of being based in various locations across Europe, including options for remote work. If you are passionate about improving patient outcomes and thrive in a dynamic environment, this opportunity is perfect for you.

Qualifikationen

• 7+ years of experience in the pharmaceutical industry with a focus on regulatory affairs.
• Experience with CCDS and EU labeling is essential.

Aufgaben

• Lead regulatory labeling discussions and manage compliance with guidelines.
• Prepare and implement regulatory documents for US and EU markets.

Kenntnisse

Regulatory Affairs

Labeling Compliance

Cross-functional Team Leadership

Pharmaceutical Industry Experience

Interpersonal Skills

Ausbildung

Bachelor's Degree in a Scientific Discipline

Advanced Degree (Masters, Pharm.D. or Ph.D.)

Jobbeschreibung

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Posted:

02.05.2025

Expiry Date:

16.06.2025

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Job Description:

With over 120 years of experience and approximately 19,000 employees in more than 30 countries/regions, Daiichi Sankyo is dedicated to discovering, developing, and delivering new standards of care that enrich the quality of life around the world.

In Europe, we focus on two areas: The goal of our Specialty Business is to protect people from cardiovascular disease, the leading cause of death in Europe, and help patients who suffer from it to enjoy every precious moment of life.

In Oncology, we are driving innovation in solid tumours and blood cancers, founded on breakthrough science from our own labs in Japan. We aspire to create better tomorrows for people living with cancer and their loved ones.

Our European headquarters are in Munich, Germany, and we have affiliates in 15 European countries and Canada.

We are seeking highly qualified candidates to fill the position of:

The position:

This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product labeling in collaboration with Global Regulatory Leads (GRLs). This position may serve as an ad hoc member of Global Project Team (GPT) to address labeling issues for late-stage projects. This position manages multiple assigned projects of increased complexity including post marketing projects and those involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data Sheets (CCDS) for assigned products. This position drives/leads the maintenance of global labeling and associated documents (including cartons and external packaging in the US) for assigned Daiichi Sankyo products. This position ensures that draft labeling complies with all applicable regulations and guidelines and with Company Core Data Sheets and manages deviations. This position interacts across the RA function globally and interacts across functional as well as regional areas. This position often works with ambiguity and complex problems, focusing on strategic and operational decisions.

This role could be filled Europe-wide, in one of the Daiichi Sankyo office locations (excluding Belgium and Greece), on site, hybrid or remote by design. Please visit our website for more information on our office locations.

• Acts as point of contact for cross-functional teams on global labeling issues
• Based on timelines or resources, may assist another Global Labeling Lead by managing labeling development or approval for either the US or EU
• Preparation of updated Core Data Sheets, and EU and US Documentation:
• Independently manages, prepares and implements regulatory documents (e.g., USPI, annotated labeling, medication guides, EU SmPC, PL, CCDS)
• Independently leads cross functional teams through all labeling discussions with the FDA/CHMP while ensuring management alignment
• Strategizes and plans for FDA meetings as needed
• Acts as point of contact for cross-functional teams on RA labeling issues
• Based on timelines or resources, may assist another Global Labeling Lead by managing labeling development or approval for either the US or EU.
• Ensure Compliance with Core Data Sheets/Label Changes:
• Manages updates to Core Data Sheets for assigned products
• Manages US/EU and local country labeling deviations from CCDS
• Ensures implementation of CCDS/labeling agreements with licensing partners
• Conduct Label Review Committee Meetings:
• Prepares documents for review by labeling teams
• Leads review processes and ensures appropriate governance for US, EU and Company Core documents as well as for the review of country labeling deviations
• Ensure Compliance with Labeling Regulations and Guidance:
• Researches applicable Health Authority labeling regulations for products and filings
• Manages compliance with internal and external guidelines, reviewing US and EU package inserts with regard to both content and format
• Follows internal processes for record keeping and tracking of labeling milestones
• Collaborates with Global Labeling Operations and Compliance Leads and other RA groups as required to produce high quality labeling documentation
• Establishes Processes and Best Practices:
• Reinforces labeling best practices at cross-functional meetings
• Assists in the development of Standard Operating Procedures (SOPs) and process improvements
• Follows agreements with external partners.
• Department Coordination: Builds cross-functional and cross-regional relationships.
• Bachelor's Degree preferably in a scientific discipline required
• Advanced degree (e.g., Masters, Pharm.D. or Ph.D.) preferred
• 7 or More Years pharmaceutical industry experience required
• 4 or More Years of direct regulatory affairs experience, including EU/US labeling experience required
• Relevant experience with CCDS and EU labeling is a must have
• Experience with ex-EU labeling (e.g. US) is a plus
• Travel - ability to travel up to 10% occasional travel
• Strong interpersonal skills and ability to effectively work with others
• Ability to work independently as well as within a team