Manager, Regulatory Intelligence

Job not on LinkedIn

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $120k - $180k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🚔 Compliance

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 0%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Zoetis

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1952

🏥 Healthcare

🍽️ Food & Beverage

🏭 Manufacturing

Healthcare • Food & Beverage • Manufacturing

Zoetis is the world's leading animal health company, committed to nurturing the world and humankind by advancing care for animals. With over 70 years of innovation, Zoetis develops a broad portfolio and pipeline of medicines, vaccines, diagnostics, and technologies that span a continuum of care to predict, prevent, detect, and treat animal illnesses. Operating in more than 100 countries, the company supports livestock farmers, veterinarians, and pet owners around the globe. Zoetis is driven by science and their shared passion for the human-animal bond, aiming to create a more sustainable and healthier world for all.

📋 Description

• Own and lead assigned global regulatory surveillance workstreams, with a focus on the USA and Canada • Monitor, interpret, and communicate evolving regulatory requirements across compendial changes, chemical requirements, packaging, diagnostics, medical devices, and GMP/Environmental inspectional activities • Coordinate cross-functional impact assessments with EHS, VMRD, Quality, Global Manufacturing, Public Affairs, and Legal • Ensure compliance plans are documented and actions are tracked to closure • Develop and distribute regulatory intelligence newsletters, regulatory watch notifications, and ad hoc query responses • Review and quality-check RI communications produced by team members • Coordinate company responses to draft guidance, standards, and consultations • Manage SME engagement, consolidate inputs, and ensure submissions reflect a clear, defensible company position • Represent the company in industry associations and regulatory forums; contribute to working groups and industry-level regulatory positions • Administer Producer Responsibility Organization obligations and Extended Producer Responsibility reporting, including data submission to state and/or national programs • Serve periodically as a subject matter expert on new and emerging regulations or requirements • Coordinate external consultant activities, including scope definition, budget review and approval, and liaison • Serve as primary contact for assigned internal stakeholder groups for regulatory intelligence inquiries • Interpret compliance trends, assess emerging risks, and prepare action plans and briefings for Governance forums • Contribute to the design, documentation, and sustainability of RI processes and SOPs • Champion AI-enabled regulatory intelligence platforms and support selection, piloting, implementation, and team training

🎯 Requirements

• Bachelor’s degree in a scientific discipline (e.g., life sciences, pharmacy, regulatory affairs, or related field) • Minimum 5 years of experience in Regulatory Affairs or related field • Demonstrated track record of independently managing regulatory deliverables and leading cross-functional workstreams or acting as Subject Matter Expert within a cross-functional team • Experience with regulatory intelligence systems or tools required at this level • Previous interactions with FDA, USDA, or other US authorities strongly preferred • Experience in a Regulatory Intelligence function preferred • General knowledge of (bio) pharmaceutical research and development, authorization and post-marketing compliance of medicinal products • Good understanding of CMC preferred • Experience as an active participant or representative in industry associations, with demonstrated contribution to working groups or policy discussions • Working knowledge of animal health product laws, regulations, and the regulatory policy-making process • Understanding of chemical substances laws and regulations • Familiarity with sustainability and packaging regulations, including US State EPR reporting frameworks and PRO data submission requirements • Experience managing a portfolio of regulatory liaison activities directly with Global Health Authorities • Hands-on experience with AI software and GenAI technology applied to regulatory intelligence workflows • All applicants must possess or obtain authorization to work in the US for Zoetis

🏖️ Benefits

• Short-term incentive compensation • Long-term incentives • Healthcare and insurance benefits beginning on day one • 401K plan with a match and profit-sharing contribution from Zoetis • 4 weeks of vacation