Evaluation and disposition of clinical supply materials with the assurance that the materials were produced in conformance to all applicable policies/procedures of our Company and compliance with all governing regulations.
Coordinate and/or support the preparation of procedures, processes and quality improvements.
Completing projects to improve the performance of our processes, including continuous process improvements, and value capture projects that seek to improve yield, reduce cost, or lower our processing cycle times.
Assists in the coordination of significant quality events including fact finding, investigation support
Collaboration across IPT functional and business areas to ensure robust processing, continuous improvement and cross-functional team building.
Actively using and championing the use of Lean Six Sigma and our company's Production System (MPS) tools, both in problem solving and day-to-day operational activities.

Minimum 2 years of experience in the pharmaceutical or equivalent industry, Good Manufacturing Practice (GMP) related field including Technical, Engineering, Quality or Operations.
Familiarity with batch disposition activities
Strong problem-solving, and written and oral communication skills
Ability to manage multiple priorities
Demonstrated teamwork skills and ability to work independently
Proficiency in the use and maintenance of Microsoft applications (Excel, Outlook, and/or MS Access, Teams)
Attention to detail, flexibility and an awareness of production and quality control problems.

medical, dental, vision healthcare and other insurance benefits (for employee and family)
retirement benefits, including 401(k)
paid holidays
vacation
compassionate and sick days

Quality Assurance Specialist

Key skills