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Quality Control Senior Associate (JP7348)

West Greenwich, RI · Biotech/Pharmaceutical
Job Title:  Quality Control Senior Associate (JP7348)
Location: West Greenwich, RI. (Onsite Essential)
Employment Type:  Contract
Business Unit: ARI Quality Control
Duration: 1+ years (with likely extensions)
Posting Date: 6/8/20
 
 
3 Key Consulting is hiring a Quality Control Senior Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company.
 
Job Description:
Our client’s Quality Control group is searching is for an analytical scientist to support testing for Raw Materials 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 will include, but are not limited to:
  • Performing analytical testing for general chemistry (pH, osmolality, appearance, etc.) per compendium.
  • 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.
 
 
Why is the Position Open?
Additional workload.
 
 
Top Must-Have Skill Sets:
  • Strong Analytical Skills – Ideal candidate will have at least 4 years of experience performing analytical testing
  • Attention to Detail – Ideal candidate will be thorough and deliver polished work product.
  • Can Do Attitude – Ideal Candidate will have a positive attitude and be willing to participate in lean initiatives on site.
 
Day to Day Responsibilities:
Daily responsibilities will be focused on executing analytical testing in a GMP laboratory.
 
 
Basic Qualifications:
  • 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
  • Experience:
    • 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
 
Preferred Qualifications:
  • 4-6 years of experience in GMP controlled analytical laboratory setting.
  • Strong project management skills.
  • Demonstrated experience in investigations and QC processes.
  • Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal supervision.
  • Strong communication skills (both written and oral), facilitation and presentation skills.
  • Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories.
  • Compendial experience.
  • Understanding of biopharmaceuticals process and related unit operations.
  • Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy.
  • Independent, self-motivated, organized, able to multi-task in time-sensitive environments.
 
Employee Value Proposition:
Opportunity to join a dynamic team and gain additional GMP testing experience.
 
Red Flags:
Candidate has no lab or industry experience.
 
Interview process:
Video Skype Panel Interview.
 
 
We invite qualified candidates to send your resume to resumes@3keyconsulting.com.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
 
 
Regards,
 
3KC Talent Acquisition Team
 
 
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