3 Key Consulting
3 Key Consulting

119 3 Key Consulting Quality Control Associate Jobs Hiring Near You

Quality Control Associate

Tucson, AZ · On-site

$23 - $25/hr

Key Responsibilities: * Perform testing of raw materials, in‑process samples, and finished goods ... HS Diploma + 7 years experience, OR Associate's + 3 years, OR Bachelor's + * Hands‑on lab ...

They are currently looking to add a Quality Control Associate to their team. The organization offers employees the opportunity to contribute to a growing business while working alongside experienced ...

Quality Control Associate

Irvine, CA · On-site

$21 - $25/hr

We are seeking a meticulous and detail-oriented Quality Control Associate to join our team. The ... 1-3 years of experience in quality control or quality assurance roles. * knowledge of quality ...

This includes working with employees as well as outside agencies or consultants involved in ... be refreshed within 3 months of hire. * OSHA-10 certification. * 2 years of data center ...

The Quality Control Raw Materials Associate I is responsible for contributing to key functional, tactical, strategic and operational aspects of the Quality Control Raw Materials group at the Client ...

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Associate Quality Control - (JP10231)

Associate Quality Control - (JP10231)

3 Key Consulting

Thousand Oaks, CA

Other

Posted 7 days ago


Job description

Job Title: Associate Quality Control - (JP10231)
Location: Thousand Oaks, CA. 91320
Employment Type: Contract
Business Unit: Quality Control Chemistry and Biochemistry
Duration: 1+ years (with likely extensions)
Notes: Only qualified candidates, please. See must have skills.
Posting Date: 05/11/22
3 Key Consulting is hiring an Associate Quality Control for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Under general supervision, this position will perform routine procedures and testing in support of the High Throughput lab (HTL) group. This position will be responsible for one or more of the following activities:
  • Performing routine laboratory procedures.
  • Routine analytical testing.
  • Documenting, computing, compiling, interpreting and entering data.
  • 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 logbooks.

Why is the Position Open?
Supplement additional workload on team.
Top Must-Have Skill Sets:
  • Prior Lab Experience.
  • cGMP Experience.
  • Chemistry/Biochemistry background.

Day to Day Responsibilities:
  • Routine analytical testing.
  • Documenting, computing, compiling, interpreting and entering data.
  • 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 logbooks.
  • General Lab housekeeping.

Employee Value Proposition:
Unique experience and opportunity
Red Flags:
Lack of lab experience.
Interview process:
Phone screening followed by in-person interview.