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Quality Control Senior Associate (JP9251)

West Greenwich, RI · Biotech/Pharmaceutical
Job Title:  Quality Control Senior Associate (JP9251)
Location: West Greenwich, RI. 02817
Employment Type:  Contract
Business Unit:  ARI Quality Control Bio-analytics and Raw Materials
Duration: 2+ years (with likely extensions)
Note: Onsite Essential Worker
Posting Date: 10/06/2021


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:
  • Targeting candidates with 4-6 years of industry/ non academia experience and some Capillary electrophoresis experience
  • Quality Control Separation Sciences lab is searching is for an team member to support testing for routine, in-process, and stability samples.
  • This person will be responsible for working in the Quality Control 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 CE (capillary electrophoresis, SDS-PAGE, polysorbate extraction and other general chemistry testing.
    • 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 on team.

Top Must-Have Skill Sets:
  • Capillary Electrophoresis and/or Empower Data Chromatography software
  • Full understanding of QC operation and GMP/GDP
  • Desire for problem solving/ continuous improvement

Day to Day Responsibilities:
  • Routine testing and lab upkeep
  • Accountability for achievements each day
  • Team and communication

Basic Qualifications:
  • 4-6 years of experience in CE or SDS-PAGE
  • Bachelors Degree in any science field
  • 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, preferably with GMP 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:
Great biotech/pharma to work for.

Red Flags:
  • Short work history.
  • Academia or R&D roles only.

Interview process:
Phone screening followed by in-person 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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