This position involves participating in site planning meetings that influence QC commercial testing plan, understanding samples demands and corresponding standardized QC test scheduling, helping QC leaders on the assignment of QC tests to be aligned on the business plan (E2E and NPL) This role requires limited supervision and strong initiative in automating, optimizing, and visualizing complex data sets to enable confident decision-making across laboratory stakeholders in regards QC tests commitment dates and releases *ESSENTIAL AREAS OF RESPONSIBILITY**
A minimum of 5 years’ relevant progressive experience in a GMP regulated environment, preferably within pharmaceuticals experience in a supply chain or planning analytics role; or an equivalent combination of education and experience *Skills/Knowledge/Abilities:**
Excellent verbal, written, and interpersonal skills required *Problem Solving:**
Additional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more. *Already Working @Company?**