Associate Quality Control, Biopharma (JP100171)
Company: 3 Key Consulting
Location: West Greenwich
Posted on: April 3, 2026
|
|
|
Job Description:
Job Title: Associate Quality Control, Biopharma (JP100171)
Location: West Greenwich, RI. Employment Type: Contract Business
Unit: Quality Control, Bio-Analytics, and Raw Materials Testing
Duration: 2 years with likely extension or conversion to FTE
Posting Date: 5/5/2022 Notes: 100% onsite 3 Key Consulting is
hiring an Associate Quality Control for a consulting engagement
with our direct client, a leading global biopharmaceutical company.
Job Description: Experience with LIMS would be a great preference -
analytical data reporting system Compendia experience is a plus but
not required Lab experience is a must (pro or academia) Overview:
Quality Control is searching is for an analyst to support routine
testing of Raw Materials. 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.), 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
Experience: Bachelor’s degree OR Associate's degree and 1-2 years
of Quality or Analytical Laboratory experience Preferred
Qualifications: 1-3 years of experience in GMP analytical
laboratory Experience with bench chemistry Experience with
Compendial testing 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. 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. Demonstrated experience in
investigations and QC processes Why is the Position Open? Staff
augmentation. Top Must-Have Skill Sets: Strong Analytical Skills
Must have lab experience - (pro or academia) Bachelor’s
degree/Associates or Highschool degree with 1-3 years of experience
in GMP analytical laboratory Understanding and application of
principles, concepts, theories and standards of GMP QC analytical
laboratories. Interpersonal Skills: 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 of raw materials in a GMP laboratory.
Basic Qualifications: Quality control lab experience and use of
HPLC/UPLC equipment is preferred Red Flags: Candidates with no
prior lab experience Interview process: Phone screening of possible
candidates. Possible second phone screen and/or in-person interview
for those who pass the initial phone screening. We invite qualified
candidates to send your resume to recruiting@3keyconsulting.com .
If you decide that you’re not interested in pursuing this position,
please feel free to look at the other positions on our website
www.3keyconsulting.com/careers. You are welcome to also share this
opportunity with anyone you think might be interested in applying
for this role. Regards, 3KC Talent Acquisition Team
Keywords: 3 Key Consulting, Hamden , Associate Quality Control, Biopharma (JP100171), Science, Research & Development , West Greenwich, Connecticut
