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Regulatory Affairs Associate

Abbott
Abbott
1-3 years
$26 - 29 per hour
10 Jan. 6, 2026
Job Description
Job Type: Full Time Part Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Regulatory Affairs Associate – Contract | Abbott, IL / OH, USA

Location: Lake County, IL or Columbus, OH, USA
Job Type: Contract / Temporary | 12 Months | 100% Onsite
Salary: USD 26–29 per hour
Department: Regulatory Affairs / Quality Assurance


About Abbott

Abbott is a global healthcare leader dedicated to helping people live healthier lives across all stages. With a portfolio spanning diagnostics, medical devices, nutrition, and branded generic medicines, Abbott drives innovation and life-changing breakthroughs worldwide.

Abbott collaborates with top talent to deliver regulatory excellence and ensure compliance with global standards in healthcare.


Role Overview

The Regulatory Affairs Associate (Contract) will support Regulatory Operations by assisting in regulatory projects and ensuring compliance with internal policies and global regulatory requirements. The role demands strong attention to detail, technical aptitude, and effective cross-functional communication.


Key Responsibilities

  • Support regulatory projects by processing and reviewing quality documentation.

  • Conduct regulatory assessments to ensure deliverables meet compliance standards.

  • Maintain the accuracy, integrity, and completeness of assigned documentation.

  • Communicate effectively with cross-functional teams to address regulatory queries and documentation requirements.

  • Participate in program strategy discussions and contribute to process improvement initiatives.

  • Collaborate with Regulatory Affairs, Supply Chain, Quality Assurance, and R&D to ensure timely execution of regulatory activities.

  • Complete additional assignments as directed by management while adhering to applicable regulatory requirements.


Qualifications

  • Education: Bachelor’s degree in Nutrition, Life Sciences, or related scientific field.

  • Experience: 1–3 years in Regulatory Affairs or Quality Assurance (regulatory experience preferred).

  • Strong attention to detail and ability to work independently and collaboratively.

  • Proficiency in Microsoft Office (Word, Excel, PowerPoint), Adobe Acrobat, and SharePoint.

  • Excellent organizational, analytical, and communication skills.


Consultant Benefits (Upon Waiting Period)

  • Medical, Dental, Vision, and Prescription Drug Plans

  • Health Savings Account & Flexible Spending Accounts

  • Short-Term and Long-Term Disability Coverage

  • Critical Illness, Accident, and Hospital Insurance

  • Life Insurance and Supplemental Coverage Options

  • 401(k) Retirement Plan

  • Legal, ID Fraud, and Pet Insurance through MetLife


Why Join Abbott?

Abbott is committed to creating life-changing breakthroughs and fostering a culture of excellence. As part of the Regulatory Affairs team, you will contribute to regulatory compliance, global healthcare innovation, and operational excellence.