QA & Regulatory Documents Coordinator

Abbott Laboratories; Columbus (OH); On-site; USD 26,243 - 52,555; Full time

Benefits offered by this job

Health benefits starting day 1

Training and career development

401(k) retirement savings plan

Job summary

Abbott Laboratories in Columbus, Ohio, is seeking a Quality Assurance professional responsible for ensuring compliance with FDA regulations and maintaining the quality system. The role requires at least 2 years of QA experience and involves auditing batch records and coordinating document requirements.

Candidates should possess a High School Diploma, with an Associate's degree preferred. The base pay ranges from $19.05 to $38.15 per hour, reflecting a competitive compensation package.

Qualifications

• 2+ years of QA experience.
• Knowledge of regulatory standards for infant formula and nutritionals.
• Ability to analyze and troubleshoot complex problems.

Responsibilities

• Implement and maintain effectiveness of the quality system.
• Audit and assure accuracy of batch records.
• Reconcile product inventories.

Skills

QA experience

Strong communication skills

Analytical skills

Proficient in computer applications

Education

High School Diploma / GED

Associate's degree or higher in a technical field

Job description

Abbott Laboratories in Columbus, Ohio, is seeking a Quality Assurance professional responsible for ensuring compliance with FDA regulations and maintaining the quality system. The role requires at least 2 years of QA experience and involves auditing batch records and coordinating document requirements.

Candidates should possess a High School Diploma, with an Associate's degree preferred. The base pay ranges from $19.05 to $38.15 per hour, reflecting a competitive compensation package.