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The Judge Group

Quality Control Validation Scientist

Post Date:Jun 29, 2020Type:Full-Time
Start Date:6/29/2020Salary:
Location:US-MA-Framingham (CDP) Job Reference:668711

Job Description:
Location: Framingham (CDP), MA
Description: Our client is currently seeking a Quality Control Validation Scientist
[Additional Description]

This job will have the following responsibilities:
  • Core Responsibilities • Perform qualification in a cGMP biotech facility managing multiple complex qualification projects and providing technical assistance to less experienced team members. • Write, review and approve qualification protocols and reports as well as execute protocol. Resolve protocol discrepancies and deviations. • Evaluates new technologies platforms for implementation in the QC Laboratories. • Ensure GMP compliance of all activities performed. • Represent QC Validation in internal and external audits as required. • Ensure appropriate facility support and provide technical expertise with regards to equipment. • Review standard operating procedures. • Maintain positive relationship and network effectively across sites and organizations. • Provide project oversight and participate in cross-functional teams. • Practice safe work habits and adhere to safety procedures and guidelines. An ongoing commitment to conducting our global business according to the highest legal and ethical standards, and to continually pursue excellence in the development and delivery of all of our products and services. This includes: • Perform other additional job related duties as required. • Adhering to all applicable laws and regulations of the places in which we conduct business, as well as our Company policies and procedures. • Being honest and treating people with respect and courtesy. 
Qualifications & Requirements:
  • • Knowledge of Validation Lifecycle Approach. • Knowledge of Validation Data Integrity Principals • Ability to present technical data. • Ability to work independently on scientific projects. • Scientific technical writing ability authoring and reviewing SOPs, qualification protocols and technical reports. • Experience troubleshooting of assay and equipment issues

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The Judge Group

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