Quality Control Senior Associate - (JP10451)
Company: 3 Key Consulting
Location: West Greenwich
Posted on: April 1, 2026
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Job Description:
Job Title: Quality Control Senior Associate - (JP10451)
Location: West Greenwich, RI. 02817 Employment Type: Contract
Business Unit: ARI QC Bioanalytics Duration: 2 years (with likely
extensions) Posting Date: 06/20/22 Notes: Only qualified
candidates, please. Targeting candidates with 4-6 years of
industry/ non academia experience and some Capillary
electrophoresis experience 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: 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. Basic
Qualifications: 4-6 years of experience in capillary
electrophoresis and/or quality control setting 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. Top Must-Have Skill
Sets: Capillary Electrophorese and/or Empower experience preferred
Teamwork and collaborative mind set Must have Quality Control lab
experience and understanding of GMP expectations HPLC and UPLC
experience Day to Day Responsibilities: Routine and non-routine
testing Maintain training maintain laboratory workspace Review
documents Red Flags: R&D experience only Frequent job changes
Interview process: Video conference call (webex) with manager
and/or potential team member Second interview with team if required
(webex) 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
Keywords: 3 Key Consulting, Plymouth , Quality Control Senior Associate - (JP10451), Science, Research & Development , West Greenwich, Massachusetts
