Quality Assurance Associate

Job Summary

This contract role is for a meticulous Quality Assurance Associate to help maintain quality systems and compliance work within the pharmaceutical and life sciences space. It is well suited to candidates at the start of their careers who want to gain experience in a regulated environment.

Key Responsibilities

• Help ensure ongoing adherence to Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) across day-to-day operations.
• Review, approve, and keep current batch records, SOPs, specifications, and other quality-related documents.
• Take part in internal audits, compliance reviews, and regulatory inspection support.
• Assist with deviation investigations, CAPA handling, and change control processes.
• Maintain accurate records and data integrity in line with company procedures and regulatory expectations.
• Work closely with teams across Manufacturing, Quality Control, Regulatory Affairs, and Supply Chain.
• Support employee training, compliance tracking, and broader quality awareness initiatives.
• Contribute to quality management system (QMS) activities while supporting FDA and other applicable industry requirements.

Required Skills

• High attention to detail
• Understanding of GMP and GDP basics
• Strong written and spoken communication
• Familiarity with pharmaceutical or life sciences workflows
• Exposure to quality systems and compliance processes
• Ability to work with cross-functional teams
• Documentation and record-keeping discipline

Additional Information

Role type: Contract

Location: Remote

Experience range: 0 to 2 years

This opportunity is aimed at recent graduates or early-career professionals who want to build a path in quality and compliance within a regulated industry.

Tools such as LIMS or TrackWise are considered an added advantage.