QA Associate (Temp) (Stanhope, NJ)

If interested, please reply with a copy of your resume. Thanks! SUMMARY This position supports essential Quality Assurance functions in a growing pharmaceutical organization. It involves maintaining documentation, assisting with compliance, supporting inspection readiness, and performing administrative tasks to ensure regulatory and internal quality standards are met. RESPONSIBILITIES • Keep current knowledge of standard operating procedures (SOPs). • Assist in delivering training initiatives across multiple teams. • Review quality assurance and quality control documentation, including logbooks. • Maintain and organize documentation systems accurately. • Input data into quality tracking databases and systems. • Support cleanroom and laboratory sanitation practices per cGLP guidelines. • Provide supporting documentation for audits and inspections. • Manage documentation issuance, tracking, and secure storage. • Oversee label issuance and participate in label counting and verification. • Ensure company and regulatory compliance is upheld across operations. • Follow all applicable current Good Manufacturing Practices (cGMP) including those in the FD&C Act Section 503B. • Support document control practices and monitor data for quality trends. • Carry out additional duties as needed to support Quality initiatives. QUALIFICATIONS • Associate degree preferred. • 2–5 years of experience in pharmaceutical or related field, or an equivalent blend of education and experience. • Strong attention to detail with excellent organization skills. • Experience using spreadsheets and databases. • Ability to manage shifting priorities and work on multiple tasks daily. • Positive team-oriented mindset with strong communication skills. • Must maintain confidentiality of sensitive information.