GMP/QC Control Analyst (ONSITE)

Overview

On Site
Depends on Experience
Contract - W2
Contract - 12 Month(s)
No Travel Required

Skills

SOP compliance
Analytical methods
cGMP
GLP
Laboratory documentation
QC testing
GMP

Job Details

Please note that this is a 12-18 month contract position.

Ideal Candidate:

  • Bachelor's degree in a life science field required.

  • Demonstrated knowledge of analytical equipment and instrumentation and experience working in a GMP environment.

  • Proven ability to coordinate and lead day-to-day tasks, collaborating with team members to meet deadlines and objectives.

Job Description:

  • Conduct routine preparations for stability, raw materials, in-process, microbiology/cleaning validation programs, and other requested testing according to Standard Operating Procedures (SOPs) and Analytical Methods in compliance with current Good Manufacturing Practices (cGMPs) and regulatory requirements.

  • Complete projects under supervision and maintain a clear understanding of Good Laboratory Practices (GLPs), cGMPs, and other regulatory requirements.

  • Exercise judgment and escalate issues appropriately to QC management.

  • Prepare solutions (e.g., mobile phases, diluents) and standard/sample preparations.

  • Follow good documentation practices consistently.

  • Work cross-functionally to complete projects and testing.

Applicants must provide their phone number. Reference job number A5054.

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