Senior Quality Control Associate

job
  • Randstad Life Sciences US
Job Summary
Location
West Greenwich ,RI
Job Type
Contract
Visa
Any Valid Visa
Salary
PayRate
Qualification
BCA
Experience
2Years - 10Years
Posted
03 Feb 2025
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Job Description

Associate Quality Control

6 Months

West Greenwich, RI

Max PR: $33.56/hr


Admin Shift (7am -3:30pm or 8am -4:30pm) Candidate can select their shift.

8 month duration with possible extension.

Ideal: Bachelor degree required, internship experience preferred but Academic experience is also fine. Candidates must have some lab experience. Nice to have: benchtop testing with instruments like GCMS HPLC.


Top 3 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:

  • Routine testing and lab operations
  • maintaining training
  • Problem solving
  • Employee Value Proposition:
  • Company experience
  • Possible Extension:
  • Yes
  • Red Flags:
  • Candidates with no lab experience.
  • Interview Process:
  • Phone screening of possible candidates.
  • Possible secondary with WebEx interviews a 1:1 and 1:4-5 for those who pass the initial phone screening.
  • We can start interviewing immediately and will be available as needed.

Job Details:

  • Under general supervision, this position will perform routine procedures to support testing within Quality Control.
  • Tasks may include but not limited to performing sample collection, sample handling, testing equipment/laboratory support.
  • This position will be responsible for one or more of the following activities:
  • Performing routine laboratory procedures
  • Documenting, computing, compiling, interpreting, and entering data into computerized systems
  • Maintaining and operating specialized equipment
  • Initiating and /or implementing changes in controlled documents.
  • Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory notebooks. Skills: some lab experience is preferred.

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