Quality Control Analyst in Northborough, MA at Pyramid Consulting, Inc

Date Posted: 6/19/2020

Job Snapshot

Job Description

Immediate need for a talented Quality Control Analyst with experience in the Pharmaceuticals Industry. This is a 06+ Months Contract opportunity with long-term potential and is located in Northborough, MA. Please review the job description below.
 
Job ID: 20-20642

Key Requirements and Technology Experience:
  • Perform operations necessary for quality testing and plays a role in implementing new technology within quality control.
  • At more senior levels, provide an investigative or technological orientation in designing, executing, interpreting and validating quality procedures and test methods.
  • Complete routine testing of raw materials, in-process and final products in accordance with SOPs for product release and validation.
  • Aid in the development of test methods.
  • Conduct data review and preliminary evaluation of results.
  • Solve problems using limited predetermined options such as repeating the assay when parameters are not met to determine the cause, etc.
  • Provide input to the technical composition of operating documentation.
  • Work is closely supervised.
  • Follows standard practices to obtain solutions.
  • Contribute to the completion of routine technical tasks.
  • Failure to achieve results can normally be overcome without serious effect on schedules and programs. Contacts are primarily with immediate - and other personnel in the section or group.
  • Demonstrate proficiency in a task by completing On the Job Training.
  • Maintain on-time completion of all training requirements.
  • Perform all activities adhering to strict cGMP guidelines.
  • Participate in department initiatives to support continuous improvement
  • Perform environmental monitoring and clean room activities
  • Sample raw materials in accordance with SOP’s
  • Perform testing and inspection in accordance with SOP’s
  • Review peer data including data transcription, data calculation and log entries.
  • Lab general duties including cleaning, glassware, washing etc.
  • Initiate DCRs when assigned.
  • Participate in audits.
  • Perform PM calibration on lab equipment.
  • Conduct Safety and weekly compliance walkthroughs.
  • Participate in Lab Investigations and NCMR investigations.
  • Adhere to site Quality and Safety Policies.
  • Work towards accomplishment of Site Goals.
Our client is a leading Pharmaceuticals Industry and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration. 
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