Senior Manager, Global Labeling Compliance & Connectivity
Senior Manager, Global Labeling Compliance & Connectivity

Senior Manager, Global Labeling Compliance & Connectivity

Full-Time 48000 - 72000 £ / year (est.) No home office possible
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BeOne Medicines

At a Glance

  • Tasks: Lead global labeling compliance projects and enhance efficiency in the labeling process.
  • Company: BeOne, a passionate biopharmaceutical company dedicated to fighting cancer.
  • Benefits: Competitive salary, professional development, and a collaborative work environment.
  • Why this job: Join a mission-driven team making a real difference in cancer treatment.
  • Qualifications: 7+ years in pharmaceutical labeling and strong project management skills required.
  • Other info: Opportunity for growth and leadership in a dynamic, global setting.

The predicted salary is between 48000 - 72000 £ per year.

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. We look for scientific and business professionals who are highly motivated, collaborative, and share our passionate interest in fighting cancer. BeOne is a global biopharmaceutical company dedicated to the discovery and development of innovative drug therapies for the treatment of cancer.

This role will support global commercial labeling projects and programs connected to labeling process effectiveness, efficiency and compliance, including external collaboration initiatives (SDEA labeling compliance) and internal collaboration initiatives across the broader BeOne organization. It requires effective cross-functional collaboration, detailed analyses, and understanding of interdependencies to support a wide range of project planning/management and infrastructure/process activities.

Responsibilities:

  • Monitor and update labeling provision of SDEA labeling contracts, including coordinating with legal and country representatives on updates and taking action if non-compliance occurs.
  • Data remediation activities.
  • Records quality events for regulatory labeling team and monitors assigned CAPAs until issue resolution and closure.
  • Drives cross-functional working groups to identify, assess, design and/or implement improvement opportunities to measure and reduce compliance risk and increase efficiency of the end-to-end Labeling process.
  • Demonstrates strong leadership and problem-solving skills and ability to gather relevant facts and distill information.
  • Assists with development, revision and maintenance of departmental SOPs, WIs and non-governance documents.
  • Prepares necessary training and communication to relevant stakeholders to ensure proper process execution.
  • Reporting out of or coordinates the timely availability of metrics and KPIs to demonstrate labeling process compliance and efficiency.
  • Serves as strategic regulatory partner and a liaison between the Global Labeling Business Users of the Systems to IT for new or enhanced technical solutions.
  • Identifies industry trends and evaluates impact on BeOne labeling policies and practices.
  • Supports development of project strategies within teams and the department.
  • On an ad-hoc basis, supports the preparation of labeling deliverables, for submission to Health Authorities, implementation on market, inspection or audit.
  • Communicates with and provides services to a wide range of internal and external contacts.
  • Anticipates and resolves problems, updates supervisor on status of projects.

Experience:

  • 7+ years pharmaceutical or industry related labeling experience, including significant examples of involvement in regulatory labeling updates and/or process.
  • Direct working experience with labeling process, document management, international labeling differences in execution such as translations, readability, harmonization etc.
  • Strong aptitude for authoring documentation such as User Guidance and Standard Operating Procedures (SOP) and change control management is desirable.
  • Familiarity with Regulatory Information Management systems.
  • Effective communication skills (verbal and written).
  • Ability to work cooperatively with others and provide significant contributions as a member of a team in addition to serving in a leadership capacity.
  • Strong organizational skills.
  • Proficiency in MS Office and Project Management tools is mandatory.
  • Familiarity of GMP requirements and working in a highly regulated industry.
  • Good understanding of GxP/GMP applications.

Qualifications:

  • Bachelor’s degree in Project Management, Life Sciences, or other related area, with at least 7 years of applicable experience in pharmaceutical or biotechnology/device industry.
  • Preferred Education: Advanced degree.
  • Prior commercial regulatory labeling required. Project management a plus.

Skills & Tools:

  • Ability to work in a strong technical environment, MS Office Suite, knowledge of Project Management tools, Labeling implementation and tracking systems, Document Management Systems, Packaging and Artwork Management Systems, Veeva Vault, Change Management Systems, SharePoint and other technical applications used in the regulatory environment.

Travel: Infrequent; national travel for team meetings and conferences, infrequent international travel.

Core Competencies, Knowledge & Skill Requirements:

  • Analytical and process minded with a short learning curve for systems and processes to drive results based on specified objectives.
  • Strong planning, organizing, and execution skills.
  • Ability to proactively manage workload and meet deadlines.
  • Ability to provide and apply creative solutions to maintain workflow.
  • Ability to work collaboratively within a global team setting, and with staff of different backgrounds and experience levels, listen to and consider stakeholder feedback.
  • Logical problem-solving skills, looks beyond immediate problems to consider root causes and addresses them.
  • Excellent verbal and written skills with great attention to detail.
  • Possess a high degree of personal responsibility, proactivity and agility.

Communication & Interpersonal Skills:

  • Fosters open communication. Listens and facilitates discussion.
  • Strong negotiating skills and ability to think creatively and develop creative solutions.
  • Proven ability to build trust and respect within the organization.
  • Ability to prioritize and handle multiple projects simultaneously.
  • Interacts with internal stakeholders and cross-functional team members, as required.

Global Competencies:

  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity

We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.

Senior Manager, Global Labeling Compliance & Connectivity employer: BeOne Medicines

BeOne is an exceptional employer, offering a dynamic work environment where passionate professionals can thrive in the fight against cancer. With a strong emphasis on collaboration and innovation, employees benefit from extensive growth opportunities, a supportive culture, and the chance to contribute to meaningful projects that make a real difference in patients' lives. Located in a vibrant area, BeOne fosters a sense of community and teamwork, ensuring that every team member feels valued and empowered to excel.
BeOne Medicines

Contact Detail:

BeOne Medicines Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Manager, Global Labeling Compliance & Connectivity

✨Tip Number 1

Network like a pro! Reach out to your connections in the biopharmaceutical industry, especially those who work at BeOne or similar companies. A friendly chat can lead to insider info about job openings and even referrals.

✨Tip Number 2

Prepare for interviews by researching BeOne's recent projects and initiatives. Show that you’re not just interested in the role but also passionate about their mission to fight cancer. Tailor your answers to reflect how your experience aligns with their goals.

✨Tip Number 3

Practice your problem-solving skills! Be ready to discuss specific examples of how you've tackled compliance issues or improved processes in your previous roles. This will demonstrate your analytical thinking and ability to drive results.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining the BeOne team and contributing to their mission.

We think you need these skills to ace Senior Manager, Global Labeling Compliance & Connectivity

Regulatory Labeling Experience
Project Management
Cross-Functional Collaboration
Data Remediation
SOP Development
Document Management Systems
Labeling Implementation
Analytical Skills
Problem-Solving Skills
Attention to Detail
Communication Skills
Organisational Skills
GMP Knowledge
Technical Aptitude
Stakeholder Engagement

Some tips for your application 🫡

Tailor Your Application: Make sure to customise your CV and cover letter to highlight your relevant experience in regulatory labeling and compliance. We want to see how your background aligns with our mission to fight cancer!

Showcase Your Skills: Don’t forget to emphasise your strong communication and organisational skills. Mention any specific tools or systems you’ve used, like document management systems or project management tools, as these are key for the role.

Be Clear and Concise: When writing your application, keep it clear and to the point. Use bullet points where possible to make it easy for us to see your achievements and qualifications at a glance.

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity at BeOne!

How to prepare for a job interview at BeOne Medicines

✨Know Your Stuff

Make sure you brush up on your knowledge of global labeling compliance and the specific processes involved. BeOne is looking for someone with a solid understanding of regulatory requirements, so be prepared to discuss your experience in detail, especially any relevant projects you've worked on.

✨Show Your Collaborative Spirit

Since this role involves cross-functional collaboration, think of examples where you've successfully worked with diverse teams. Highlight your ability to communicate effectively and how you’ve contributed to team success in previous roles.

✨Be Ready to Problem-Solve

Prepare for situational questions that test your problem-solving skills. Think about challenges you've faced in labeling compliance and how you approached them. BeOne values creative solutions, so don’t hesitate to share innovative ideas you’ve implemented.

✨Demonstrate Your Leadership Skills

Even if you're not applying for a direct management position, showcasing your leadership abilities is key. Discuss instances where you've taken initiative or led a project, particularly in a regulatory context, to show you can drive results and inspire others.

Senior Manager, Global Labeling Compliance & Connectivity
BeOne Medicines
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