BMS Services Sp. z o.o. Posted August 11, 2026

Director, Global Labeling Strategy, Team Leader

Warsaw-WeWork-PL, Poland Full time
Regulatory Affairs Director

BMS Services Sp. z o.o. is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Working with Us

Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .

The Director, Global Labeling Strategy Team Lead - based in Warsaw - provides strategic leadership and oversight for a team of Global Labeling Strategists, driving labeling excellence especially across the Marketed Products Portfolio while shaping regulatory labeling strategy, policy, and innovation together with the Head of Global Labeling and relevant internal and external stakeholders.

Responsibilities:

Responsible for a team of Global Labeling Strategists primarily supporting the Marketed Product Portfolio

As part of the Global Labeling Leadership team, contributes to build and execute the Global Labeling Strategy and Vision

Acts as a strategic voice for Global Labeling

Provides leadership and development for direct reports, establishing a framework facilitating knowledge sharing

Builds a strong, future‑ready labeling organization through coaching, mentoring, succession planning, and capability development.

Manages direct reports to ensure coverage for assigned products

Ensures that Program Deliverables are met and labeling claims across programs / TA are consistent (including beyond the Marketed Product Portfolio)

Leads key initiatives (Process Improvements, Development of new tools, technologies) to support efficient global label development and worldwide submissions, reviews and approvals

Identifies opportunities to influence regulatory policy and climate with respect to labeling content

Ensures effective planning of all cross-functional labeling activities

Champions labeling modernization through digital labeling, structured content, data‑driven processes, and AI‑enabled solutions to improve speed, quality, and sustainability.

Degree Requirements:

Masters of Life Sciences or equivalent, with thorough understanding of scientific principles and at least 10 years of Labeling / Regulatory Experience; Bachelor of Lifesciences with at least 15 years of Labeling / Regulatory Experience;

At least experience with one NME submission or Extension of Indication globally

Advanced Academic Training (PharmD, PhD, MD) highly desirable

Key Competency Requirements :

Experience in people management, including but not limited to the development and management of (a) high performing team(s), with involvement of remote team members

Knowledge of Global Labeling Guidances, Drug Development and Commercialization of prescription medicines

Proven understanding of the dynamics and purpose of the Company Core Data Sheets (CCDS) and the implications of the CCDS

Proven ability to understand regulatory implications of product strategy related to labeling development, assessment and management

Demonstrated ability to develop strong and positive working relationships across diverse teams and within a global environment

Proven Matrix leader with excellent problem-solving skills

Ability to influence and lead a diverse group of Subject Matter Experts from a variety of disciplines and facilitate discussions and decision making

Proven ability to develop and manage a highly competent and technically skilled team

Experience in managing high to medium complex projects

Excellent verbal and written communication skills

Keen attention to detail and accuracy

Ability to assimilate clinical and scientific information and present it in a concise manner

Ability to think creatively and good excellent problem-solving skills

Travel maybe required

#LI-Hybrid

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Compensation Overview:

Warsaw - PL: zł541,830 - zł656,574


The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. The final compensation will be determined based on demonstrated experience and in accordance with pay equity principles and applicable employment laws.

Uniquely Interesting Work, Life-changing Careers

With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected] . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:  https://careers.bms.com/california-residents/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection .

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at [email protected] . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R1601866 : Director, Global Labeling Strategy, Team Leader

Job details

Seniority
Director
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Warsaw-WeWork-PL, Poland
Employment type
Full time

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 74 comparable Director Regulatory Affairs roles across 22 biopharma companies.

74Comparable roles tracked
59Currently active
22Companies hiring similar roles
9Countries represented

Salary context

34 of 74 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Peer group range $174,000 – $295,900 (median $244,150)

Where these roles are based

Top locations among the 74 comparable roles

United States49
Ireland8
United Kingdom7
Poland3
China's Mainland2
Spain2

+ 3 more countries

Seniority mix

74 of 74 peers have a known seniority level

Director60
Senior Director12
Principal2

Therapeutic area mix

9 of 74 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology3
Cardiovascular / CVRM2
Respiratory2
Rare Disease1
Neuroscience1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
BMS Services Sp. z o.o. Warsaw, Poland Director
Same function Same seniority Same country
60%similar
AstraZeneca Warsaw, Poland Director
Same function Same seniority Same country
60%similar
AstraZeneca Warsaw, Poland Director
Same function Same seniority Same country
45%similar
AbbVie Director
Same function Same seniority

Open in 4 locations

North Chicago, United StatesFlorham Park, United StatesCambridge, United StatesIrvine, United States

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Director, Global Scientific and Regulatory Documentation, Content Strategy
BMS Services Sp. z o.o. · Warsaw, Poland · Director
Function Therapeutic area Seniority Country
45%
Director, RA Global Regulatory Strategy
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
45%
Director, RA Global Regulatory Strategy
AbbVie · Cambridge, MA · Director
Function Therapeutic area Seniority Country
45%
Director, RA Global Regulatory Strategy
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.