Quality Control Scientist in Framingham, MA at Pyramid Consulting, Inc

Date Posted: 6/29/2020

Job Snapshot

Job Description

Immediate need for a talented Quality Control Scientist with experience in the Pharmaceuticals Industry.This is a 04+ Months Contract opportunity with long-term potential and is located in Framingham, MA. Please review the job description below.
 
Job ID: 20-20233

Key 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 habits and adhere to Genzyme’s 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.
  • 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.
  • Constantly striving to make Genzyme a great place to , and a company respected for the quality of its people and products.
Key Requirements and Technology Experience:
  • Knowledge of Validation Lifecycle Approach.
  • Knowledge of Validation Data Integrity Principals.
  • Ability to present technical data.
  • Ability to independently on scientific projects.
  • Scientific technical writing ability authoring and reviewing SOPs, qualification protocols and technical reports.
  • Experience troubleshooting of assay and equipment issues.
Our client is a leading Pharmaceuticals Industry and we are currently interviewing fill this and other similar contract positions. If you are interested in this position, please apply online to for immediate consideration. 
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