What are the responsibilities and job description for the Quality Assurance Associate position at Planet Pharma?
The Opportunity: Quality Assurance Associate
- Support the Quality Assurance (QA) team in maintaining compliance with internal procedures, regulatory requirements, and quality standards.
- Assist with the review, organization, and maintenance of quality documentation, including SOPs, training records, and quality records.
- Participate in quality system activities such as deviations, CAPAs, change controls, and document control processes.
- Collaborate cross-functionally with Manufacturing, R&D, and other teams to support quality initiatives and continuous improvement efforts.
- Gain hands-on experience in a regulated biotech/pharmaceutical environment while developing a foundational understanding of GMP and quality systems.
- Currently pursuing a Bachelor’s or Master’s degree in Life Sciences, Engineering, Chemistry, Biology, Biotechnology, or a related field.
- Strong attention to detail with the ability to follow written procedures and maintain accurate records.
- Basic understanding of quality principles or regulated environments (academic coursework acceptable).
- Proficiency with Microsoft Office (Word, Excel, PowerPoint); ability to learn electronic quality management systems (eQMS).
- Strong written and verbal communication skills.
- Ability to work independently as well as collaboratively in a team environment.
- Prior internship, coursework, or laboratory experience in GMP, GxP, QA, QC, or manufacturing environments.
- Familiarity with FDA regulations, ICH guidelines, or ISO standards.
- Experience with document control systems, quality databases, or data analysis tools.
- Demonstrated interest in quality assurance, regulatory affairs, or compliance-focused career paths.