GMP Quality Assurance Associate needs 5+ years of GMP Quality Control Laboratory knowledge and/or experience in API or finished product manufacturing, QA or Engineering. GMP Quality Assurance Associate requires: • BS in a science-related field such as Pharmacy, Chemistry, Biological Sciences or related Life Sciences • Testing experience with Small Molecule • Thorough technical understanding of quality systems and regulatory requirements relating to quality control laboratories • Knowledge of pharmaceutical manufacturing operations. • Demonstrated coaching and mentoring skills. • Experience in root cause analysis. • Demonstrated application of statistical skills. • Demonstrated strong written and verbal communications skills. • Strong attention to detail. • Proficiency with computer system applications. • Excellent interpersonal skills and networking skills. • Ability to organize and prioritize multiple tasks. • Ability to influence diverse groups and manage relationships. • BS in a science-related field such as Pharmacy, Chemistry, Biological Sciences or related Life Sciences. • GMP Quality Assurance Associate duties: • Assess the impact of analytical deviation investigations and changes and ensure that all appropriate records are documented and retrievable. • Maintain awareness of external regulatory agency findings which individually or collectively reference the quality of the product. • Review and approve documents including, but not limited to, analytical procedures, change control proposals, deviations, analytical equipment qualifications, analytical methods and computerized system validations. • Participate in projects to improve productivity.