At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

JOB SUMMARY:

The Senior Specialist, Artwork Coordinator is the primary point of contact and is responsible for the end-to-end coordination and project management of artwork changes and lifecycle activities for assigned products and markets within the Manufacturing Science & Technology (MS&T) organisation.  The role is responsible for managing artwork projects from initiation through implementation, ensuring artwork deliverables are completed accurately, on time and in compliance with regulatory, quality and business requirements. The Senior Specialist will develop and maintain project plans, coordinate cross-functional activities, and drive alignment between internal stakeholders and external partners to ensure successful execution of artwork changes.

Working closely with Regulatory, Quality, Supply Chain, Manufacturing, Packaging, Contract Manufacturing Organisations (CMOs) and artwork service providers, the Senior Specialist will ensure timely delivery and implementation of artwork updates while maintaining continuity of supply. The role will also serve as the key contact for artwork-related activities, support process improvements, monitor project performance and provide metrics and reporting to support operational excellence across the artwork function.

Key Responsibilities:

• Coordinate artwork change requests from initiation through approval and implementation, ensuring timely delivery and compliance with regulatory and company requirements.

• Serve as the primary point of contact for artwork-related activities, collaborating with Regulatory, Quality, Manufacturing, Supply Chain and external manufacturing partners.

• Manage and maintain artwork records, databases and tracking systems to ensure accurate control, status visibility and reporting of artwork changes.

• Support Contract Manufacturing Organisations (CMOs) in the planning, implementation and lifecycle management of artwork changes across commercial product portfolios.

• Drive continuous improvement of artwork and change management processes, including support for investigations, CAPAs and compliance with cGMP and quality requirements

Education and Experience:

·     Relevant qualification in related field or equivalent

·     3+ years’ experience in a similar role

·     A good understanding of packaging components and the packaging manufacturing process

·     Knowledge of regulatory and quality requirements for pharmaceutical artwork

·     Computer literate

·     Knowledge of artwork proofing software

·     Supply Chain and Planning processes experience is desirable

Essential Skills and abilities:

·     Detail and high focus on accuracy

·     Ability to manage multiple change projects whilst ensuring Compliance and Supply to Market requirements

·     Communication and Interpersonal skills

·     Organization and coordination skills

Why you should apply

• You will help patients in their fight against serious diseases
• You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees.
• You’ll get a competitive salary and a great benefits package including, but not only, an annual bonus, pension contribution, family health insurance, 27 days of annual leave, and life assurance 

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

How We Work

Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

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 qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only:  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 this posting is missing required information required by local law or incorrect, contact BMS at [email protected] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.