Regulatory Specialist II

Abbott; South Portland (ME); Presencial; USD 90.000 - 120.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical and Prescription Drug Plans

Dental Plan

Vision Plan

Health Savings Account

Flexible Spending Accounts

MetLife Insurance Options

Descripción de la vacante

Abbott in South Portland, ME seeks a Regulatory Specialist II to manage IVDR-compliant technical writing and regulatory support for diagnostic products. The role develops regulatory strategies for EU and international approvals, supports regional teams with submissions and license amendments, and maintains ongoing marketing authorizations.

Responsibilities include preparing submission documents, organizing files, and training stakeholders while ensuring compliance with ISO, FDA, and other

Formación

• Bachelor’s degree in science or engineering field.
• 4+ years in Regulatory Affairs role.
• Strong knowledge of IVDR and EU regulatory requirements.

Responsabilidades

• Prepare regulatory files under IVDR requirements.
• Support regulatory submissions and license renewals.
• Develop strategies for EU/international clearances.
• Maintain approvals and track regulatory changes.
• Create internal procedures and training for stakeholders.
• Organize department files and ensure documentation.
• Assist regional teams with submissions and amendments.
• Ensure compliance with ISO, FDA, and other agencies.

Conocimientos

EU regulations

Regulatory writing

Verbal communication

Time management

Independent work

MS Office

Skills-Based Hiring

Educación

Bachelor’s degree in science/engineering

4+ years Regulatory Affairs

IVDR knowledge

Descripción del empleo

Title: Regulatory Specialist II

Location: South Portland, ME

Duration: 12 Months

100% Onsite

Responsibilities:

• Responsible for technical writing of files in accordance with In Vitro Diagnostic medical device Regulation (IVDR).
• Provides regulatory support for diagnostic product development and commercial diagnostic products.
• Develops regulatory strategies for products in development and for modified products to achieve clearance/approval in the EU and internationally.
• Provides regulatory support to regional regulatory teams to assist with submissions, license renewals, and license amendments.
• Researches and communicates scientific and regulatory information in order to write submission documents.
• Compiles and publishes all material required for submissions, license renewals, and annual registrations.
• Maintains approvals/licenses/authorizations for existing marketing authorizations.
• Assesses product, manufacturing, and labeling changes for regulatory reporting impact and compliance to regulations.
• Develops internal procedures and tools.
• Conducts informational or training sessions for stakeholders.
• Organizes and maintains hard copy and electronic department files.
• Demonstrates commitment to the development, implementation and effectiveness of Abbott Quality Management System per ISO, FDA, and other regulatory agencies.
• Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices.

Education:

• Bachelor’s Degree in Biology, Chemistry, Biochemistry, Engineering or other related technical field or the equivalent combination of education and experience.
• 4+ years’ experience in Regulatory Affairs role.
• Strong knowledge of IVDR and EU regulatory requirements is required.

Preferred Qualifications:

• 1+ years’ experience in an IVD or medical device manufacturing environment.

Competencies:

• Good knowledge of EU and international regulations.
• Demonstrated written and verbal communication skills.
• Strong time management skills, with the ability to work on multiple projects simultaneously.
• Ability to work independently as well as within a team.
• Proficiency with Microsoft Office, including Word, Excel, PowerPoint and Visio
• Enable Skills-Based Hiring

Consultants Eligible Benefits Upon Waiting Period:

• Medical and Prescription Drug Plans
• Dental Plan
• Vision Plan
• Health Savings Account (for High-Deductible Health Plans)
• Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
• Supplemental Life Insurance
• Short Term Disability (coverage varies by state)
• Long Term Disability
• Critical Illness, Hospital coverage, Accident Insurance
• MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
• 401(k)

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.

Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.