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Quality Control Senior Associate - (JP9382)

West Greenwich, RI · Biotech/Pharmaceutical
Job Title:  Quality Control Senior Associate - (JP9382)
Location: West Greenwich, RI. 02817 (Onsite)
Employment Type:  Contract
Business Unit: ARI Quality Control Bio-analytics & Raw Material Testing
Duration: 2+ years (with likely extensions and/or conversion to permanent)
Posting Date: 10/28/2021


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:
*Candidate will be working on site
**Targeting candidates with 4-6 years of industry/ non academia experience.

Quality Control Raw Materials is searching is for an analytical scientist to support testing for Raw Materials of routine samples for use within our network manufacturing operations.
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 HPLC, UPLC, Gas Chromatography, GC-MS and/or IC-PMS
  • 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?
Supplement additional workload on team.

Top Must Have Skills:
  • HPLC, GC, GC-MS or ICPMS experience, pertaining to routine use and troubleshooting.
  • GMP laboratory experience.
  • Teamwork and motivation to problem solve and improve self, operations, and processes.

Basic Qualifications:
  • 4-6 years of experience in HPLC, GC, GC-MS and/or ICP/MS
  • 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
  • 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:
To work with a dynamic team.

Red Flags:
Jumpy job history.

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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