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US Manager Labeling


Smyrna, Georgia, United States

Job Function:  Regulatory Affairs
Job ID:  71648

Help us transform patients' lives.

At UCB, we put our heart, soul and skills into making a difference for people living with significant unmet needs. Working together, we blend the best of our talents to deliver thoughtful solutions that patients value. Will you join us in this pioneering adventure?





As part of the US Labeling, Advertising and Promotions (Ad Promo) team, and under the supervision of the US Labeling Ad Promo Science Lead, the Labeling Strategist Manager is responsible for the facilitation and management of the end-to-end labeling and artwork processes for pre- and post- marketed products over the product’s lifecycle. The Labeling Strategist Manager will manage the development of the United States Package Insert (USPI) in accordance with company labeling processes for assigned therapeutic area(s).


You like to work in an environment where you can: 

•    Own the development, review, approval, and maintenance of labeling for designated products. Lead the Cross Functional Labeling Team and manage labeling projects for the USPI and local labeling. This will include active research of competitive labels as well as identifying support for associated promotional claims (80%).
•    Actively participate on product development teams to provide labeling leadership and help identify labeling concept targets (5%).
•    Mentor junior staff members to help build robust internal labeling expertise (5%).
•    Prepare the submission ready labeling documents, including the SPL and packaging artwork. Maintains and tracks labeling documents in the labeling repository and electronic system, as appropriate (5%).
•    Maintain expertise in worldwide regulation changes pertaining to labeling regulations and maintain the labeling SOP and work instructions (5%).


You will contribute by:

•    Participating in the development of the labeling objectives early in product development to assist teams in creating development strategies.
•    In conjunction with regional leads, representing regional and local perspective during the development, review, approval, and maintenance of the Company Core Data Sheets (CCDS).
•    Leading the development, review, approval and maintenance of core US labeling documents including Prescribing Information, Medication Guide, Instructions for Use, packaging artwork.
•    In conjunction with the US Lead, leading the cross-functional Labeling Team and managing labeling projects for local labeling effectively and independently.
•    Providing US strategic guidance on labeling regulations and requirements.
•    Assisting in preparation of responses to labeling-related FDA questions (labeling negotiations).
•    Supporting development of labeling for HF studies.
•    Representing the labeling function on product-specific global regulatory teams.
•    Maintaining and appropriately archiving submitted and approved labeling documents and packaging component labeling.
•    Assisting in the creation or revision of the labeling SOP or work instructions.


Interested? For this position, you’ll need the following education, experience and skills


Minimum Qualifications:
•    Biotech or pharma regulatory labeling and/or advertising-promotional experience is required: with 4+ years of experience at the Manager level.
•    In-depth knowledge of the labeling process, industry practice, packaging manufacturing process, and the drug development process.


Preferred Qualifications:
•    Advanced degree preferred, but not required.
•    Experience working in a VeevaVault-based document management system a plus.
•    Knowledge and understanding of US and international labeling regulations, ICH guidelines, and related guidelines.
•    Ability to effectively utilize clinical and scientific information to create target labeling.
•    Possess strong analytical, integrative, negotiation, and conflict resolution skills.
•    Ability to maintain multiple projects and prioritize work independently.
•    Attention to detail, project and time management skills.
•    Proficient in utilizing the Microsoft Suite of software.


Why you should apply:


Do you want to contribute in bringing real value to patients living with severe diseases while driving innovation forward? Join UCB’s dynamic, inspiring and innovative environment. You will be recognized for impactful performance via a competitive compensation and benefits package and you will enjoy ample personal development opportunities.


Tell us what makes you the perfect match to our team and join one of the most dynamic & forward-looking organizations in the world. 


To apply, please go to www.ucb.com/careers.  




About Us

At UCB, we come together every day to work, laser-focused, on a simple question: How will this create value for people living with severe diseases? By putting patients at the heart of everything we do, our approach – from discovery to development to delivery – is continuously transformed and designed around patient needs and their journey.

With a team of approximately 7,500 employees worldwide operations in more than 40 countries, we are a global biopharmaceutical company investing more than a quarter of our revenue in cutting-edge scientific research. We are focused on addressing chronic, neurological, immunological, and bone diseases. We are looking for people with passion and empathy who develop a real understanding of patient’s needs and can deliver thoughtful solutions to decisionmakers across the heath care ecosystem.

Curious to know more? Please visit our website www.ucb.com.

UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.

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