QA Associate I, Pharma: Audits, CAPA & Compliance

Cedent Consulting; Nova Scotia; On-site; CAD 60,000 - 80,000; Full time

Job summary

A leading consulting firm in Nova Scotia is seeking a Quality Assurance Associate II/III. This role involves supporting the Quality Assurance Department in compliance with regulatory requirements. Candidates should possess experience in pharmaceutical, GMP environments, and strong analytical skills. The position requires full-time work of 40+ hours per week and offers opportunities for training and operational improvements.

Qualifications

• Experience in quality assurance within a pharmaceutical or GMP environment.
• Knowledge of FDA and GMP regulations.
• Strong analytical skills and attention to detail.

Responsibilities

• Conduct quality assurance audits of production and facility records.
• Support GMP investigations and validation review.
• Participate in internal/external audits and prepare reports.
• Assist in the training of staff on quality assurance processes.

Skills

Project Management

Problem Solving/Analysis

Communication Proficiency

Technical Capacity

Collaboration Skills

Education

Bachelor's degree in a relevant field

Job description

A leading consulting firm in Nova Scotia is seeking a Quality Assurance Associate II/III. This role involves supporting the Quality Assurance Department in compliance with regulatory requirements. Candidates should possess experience in pharmaceutical, GMP environments, and strong analytical skills. The position requires full-time work of 40+ hours per week and offers opportunities for training and operational improvements.