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Director, Regulatory Affairs

7-10 years
$147,300–$294,700.
10 July 4, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Director, Regulatory Affairs – Abbott Diagnostics | Lake Forest, IL (On-site)

Job Summary:

Abbott’s Diagnostics Division is seeking a Director of Regulatory Affairs to lead global regulatory strategy, compliance initiatives, and submissions across the product lifecycle. Based in Lake Forest, IL, this high-impact role requires deep regulatory expertise, strategic thinking, and leadership excellence to influence cross-functional teams, external regulatory bodies, and executive decision-making. If you are passionate about shaping regulatory pathways in diagnostics and thrive in a fast-paced healthcare environment, this opportunity is for you.


Key Responsibilities:

  • Develop and lead global regulatory strategies across all product lifecycle stages

  • Analyze and advise on regulatory trends, emerging risks, and new regulations

  • Oversee global submission planning and review (e.g., 510(k), PMA, CE mark, IDE)

  • Guide internal and external audits, FDA inspections, and post-market compliance

  • Partner with legal, R&D, quality, marketing, and manufacturing to ensure regulatory alignment

  • Represent Abbott in trade associations and external regulatory working groups

  • Lead and mentor a high-performing regulatory team; drive career development

  • Ensure adherence to global GxPs, FDA regulations, and international guidelines

  • Direct regulatory input in M&A due diligence, advertising, labeling, and promotional review

  • Lead crisis management, recalls, adverse event reporting, and risk mitigation


Required Skills & Qualifications:

  • Bachelor’s degree in biology, chemistry, engineering, or a related scientific field

  • 7–10 years of regulatory experience in diagnostics, medical devices, or pharmaceuticals

  • Strong leadership in global regulatory operations and compliance strategy

  • Expert knowledge of FDA CDRH/CDER, EU MDR, ISO 13485, GCP, GLP, GMP

  • Ability to interpret and apply international regulatory frameworks and treaties

  • Prior experience interfacing with regulatory bodies (e.g., FDA, EMA, Notified Bodies)

  • Advanced degree (MBA, MS, PhD, or JD) preferred

  • Exceptional communication and influence skills across all leadership levels


Perks & Benefits:

  • Salary Range: $147,300 – $294,700 (location-dependent)

  • Free employee medical coverage (HIP PPO) upon wellness completion

  • 401(k) with high employer contributions

  • Tuition reimbursement and education support programs (Freedom 2 Save, FreeU)

  • Paid time off and extensive career development resources

  • Inclusive work environment recognized globally for diversity and innovation


Company Description:

Abbott is a global healthcare leader, transforming diagnostics, medical devices, and nutritional science for over 160 countries. The Abbott Diagnostics Division drives health outcomes through advanced diagnostic tools, informatics, and automation, setting industry standards for accuracy and speed in medical testing.


Work Mode:

On-site – Lake Forest, Illinois, USA


Call to Action:

Are you a strategic regulatory leader ready to drive global impact in diagnostics? Apply today to join Abbott as Director, Regulatory Affairs and shape the future of healthcare innovation and compliance.