Quality Associate


Job ID 18-00039

Industry Pharma

Job Type Permanent

Location East Windsor, NJ

Description

ESSENTIAL DUTIES & RESPONSIBILITIES

50% Daily Sampling and Inspecting Finished Drug Product according to Specifications when received at our Distribution Center

25% Daily Reading Temperature Recording Devices which arrive with the Product Shipment

25% Daily Release Product and other related ativities as deemed needed

 

OTHER RESPONSIBILITIES

Contribute to writing SOPs or processing Investigations related to the department as assigned. Partake in government inspections as required.



Qualifications

QUALIFICATIONS PREFERRED & REQUIRED

0-2 years experience in Pharmaceuticals working in a technical environment being exposed to cGMPs. Some Knowledge of Microsoft Office

LEADERSHIP SKILLS & ABILITIES

Strong Communication Skills, positive workethic, integrity, homesty and focus . Strong writing skills.

MANAGEMENT SKILLS & ABILITIES

Efficient under pressure and problem solving skills relating to incoming inspection of finished drug product