When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.
How will you make an impact? As the Senior Director of Regulatory Affairs for North America, you will build and oversee the Regulatory Compliance and CMC services capabilities in North America covering chemical and biological Drug Substance and Drug Product (Clinical and Commercial) Contract Manufacturing and Development (CDMO) Services, including:
Monitoring and dissemination of US and ROW regulatory the Global network.
Interacting with PSG ( Pharma Services group) sites, sales, business management and clients to deliver Regulatory CMC services.
Ensuring site & product compliance to standards.
Establish and maintain external influence with key Health Authorities
Lead of NA Regulatory group in a matrix organization
Monitor, anticipate, pre-evaluate and communicate on major pharmaceutical regulations for PSG
Collaborate with health authorities and key industry stakeholders as to provide input on new regulatory trends and provide SME consultation to organization
Sponsor internal regulatory knowledge by developing appropriate forums
Contribute to Corporate Quality Standards, Guidelines and Positions Papers and facilitate their implementation
Develop and implement the NA Regulatory CMC service offering
Ensure local regulatory capabilities by training, guiding and growing suitable tools to enable regulatory business opportunities and associated revenues generation
Contribute to key projects in the North American region such major tech transfers and new strategic customers
Assist within regulatory quotations issuance, lead or influence regulatory strategies
Deliver ad hoc expertise on registration files relevant to items such as IND, NDA, BLA, ANDA, NADA, PAS, CBE/30, AR, and assess overall regulatory risks
Regulatory Compliance Activities
Identify opportunities for harmonization & optimization, assist in work plan definition to fulfill the gaps and follow-up on implementation and maintenance at a site level
Site compliance: oversee domestic licenses, foreign accreditation, master documents, and contribute to official regulatory inspections and key customer audits
Product compliance: collaborate and contribute to critical activities such as regulatory systems, compliance programs and quality issue resolution
Develop and maintain relationship with key Health Authorities and regulatory organization
Lead NA Regulatory Organization
Establish goals and objectives for the NA regulatory organization
Within matrix environment support elements of human resource management, including hiring, on-boarding, performance management and development
Leverage talents and develop synergies across the NA Regulatory team to deliver the business strategy and goals
Use the Thermofisher PPI (Practical Process Improvement) system to create a culture of exceptional performance
At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.
If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, click here for further assistance.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
How will you get here?
Education Bachelors degree in Life Science (ex. Pharmacy, Engineering, Chemistry, Microbiology)
Minimum 12 years of directly relevant regulatory affairs, CMC, and cGMP manufacturing operational exposure
Knowledge, Skills, and Abilities
Intimate knowledge of global regulatory environment
Proven thought leadership within Biopharmaceutical manufacturing professional communities such as PDA, RAPS, DIA and PhRMA
Significant and demonstrated ability to successfully manage, lead, and build high performing teams
Must be able to sustain travel schedule of approximately 30%, both domestic and international
Employer will assist with relocation costs.
Internal Number: 103742BR
About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with revenues of $18 billion and approximately 55,000 employees in 50 countries. Our mission is to enable our customers to make the world healthier, cleaner and safer. We help our customers accelerate life sciences research, solve complex analytical challenges, improve patient diagnostics and increase laboratory productivity. Through our premier brands – Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific and Unity Lab Services – we offer an unmatched combination of innovative technologies, purchasing convenience and comprehensive support. For more information, please visit www.thermofisher.com.