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Sr Associate Quality Control (JP7855)

West Greenwich, Rhode Island · Biotech/Pharmaceutical
Job Title: Sr Associate Quality Control (JP7855)
Location: West Greenwich, Rhode Island 02817
Employment Type: Contract
Duration: 12 months with likely extensions
Job posting date: 22 October 2020
Note: Onsite Essential
 
3 Key Consulting is hiring a Sr Associate Quality Control for a consulting engagement with our direct client, a leading global bio-pharmaceutical company.
 
Job Summary:
  • Quality Control Bioanalytics is searching is for an analytical scientist to support testing for product routine and stability samples for multiple drug substance programs.
  • This person will be responsible for working in the Quality analytical laboratory, using GMPs and GDPs to execute analytical testing.
  • The ideal candidate enjoys tackling challenges and excels at time management with attention to detail.

Responsibilities:
  • Performing analytical testing for Capillary Electrophoresis and general chemistry (pH, osmolality, appearance, etc.).
  • Interacting cross-functionally with a wide variety of people and teams.
  • Troubleshoot, solve problems and communicate with stakeholders.
  • Participate in initiatives and projects that may be departmental or organizational in scope.
  • Evaluate lab practices for compliance and operational excellence on a continuous basis.

What we are looking for:
  • Experience with analytical laboratory testing with the ability to plan and perform routine tasks with efficiency and accuracy.
  • Demonstrated ability to work independently and deliver right first time results.
  • Excellent communication skills (written and verbal).
  • Must have focus on data integrity.
  • Qualified to work in the U.S. without employer sponsorship.
  • Commitment of a 40-hour work week in West Greenwich, RI
 
Education:
Master’s degree OR  Bachelor’s degree + 2-4 years of directly related experience OR Associate's degree and 6 years of Quality or Analytical Laboratory experience OR High school diploma/GED and 8 years of Quality or Analytical Laboratory experience

Top Must have Skill Sets:
  • 2 years of general chemistry experience.
  • Experience in General chemistry analysis such as pH, Osmolality, Subvisible particles, Visual inspection, and UV.
  • Demonstrated experience in investigations, change control, validation, audits, QC processes.
  • Demonstrated ability to interpret scientific literature.
  • GMP/GDP experience
 
Employee Value Proposition:
Quality Control Laboratories are a fast-paced organization with opportunities to cross-train on several analytical assays. We are a motivated, high performing team in close proximity to manufacturing, so the candidate will get a holistic view of the drug manufacturing process.
 
Red Flags: No PhD candidates as this is a more entry level position.
 
Interview Process:  phone/skype. 
 
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to look at other positions on our website www.3keyconsulting.com. You are welcome to also share this posting with anyone you think might be interested in applying for this role.
 
 
 
 
 
Regards,
 
3KC Talent Acquisition Team
 
 
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