Global Regulatory Portfolio Manager

Bristol-Myers Squibb; Poland; On-site; PLN 179,000 - 217,000; Full time

Job summary

Bristol Myers Squibb in Warsaw, Poland, is seeking a Regulatory Operations Associate to coordinate and support cross-functional regulatory teams in delivering portfolio commitments in line with global processes and local requirements.

You will lead GRST meetings, track health authority milestones, and assist with regulatory submissions, analytics, and information management while sustaining rigorous compliance and continuous improvement.

Qualifications

• Bachelor degree in natural science or pharmacy or related healthcare field
• ≥ 3 years in pharmaceutical industry and regulatory experience
• Solid understanding of major Health Authority regulations (FDA, EMA, MHRA) and regulatory standards
• Excellent communication and organizational skills with meticulous attention to detail
• Ability to lead cross-functional teams and negotiate with regulatory authorities

Responsibilities

• Coordinate and support cross-functional regulatory teams to deliver portfolio milestones in compliance with global processes and local requirements
• Facilitate GRST meetings and follow up to drive decisions and accountability
• Execute regulatory strategy, maintain regulatory BoW, and track health authority milestones
• Support global regulatory submissions and preparation of data for GRT discussions
• Monitor regulatory landscape and provide regulatory intelligence and policy input
• Maintain Regulatory Information Management records and support product divestitures or integrations
• Identify opportunities for process improvements and analytics in regulatory operations

Skills

Communication skills

Organizational skills

Attention to detail

Decision making

Cross-functional teamwork

Education

Bachelor degree in natural science or pharmacy

Job description

Bristol Myers Squibb in Warsaw, Poland, is seeking a Regulatory Operations Associate to coordinate and support cross-functional regulatory teams in delivering portfolio commitments in line with global processes and local requirements.

You will lead GRST meetings, track health authority milestones, and assist with regulatory submissions, analytics, and information management while sustaining rigorous compliance and continuous improvement.