GMP/QC Quality Analyst (Onsite)

Boulder, CO, US • Posted 2 days ago • Updated 10 hours ago
Contract W2
No Travel Required
On-site
Depends on Experience
Fitment

Dice Job Match Score™

⭐ Evaluating experience...

Job Details

Skills

  • GMP
  • GLP
  • Analytical Equipment
  • Instrumentation
  • Solution Preparation
  • Sample Preparation
  • Microbiology
  • Cleaning Validation
  • SOP Compliance
  • Documentation
  • Project Coordination
  • Team Collaboration
  • Communication
  • Problem Solving
  • Regulatory Compliance
  • Laboratory Practices
  • Equipment Maintenance
  • Time Management

Summary

Please note that this is a 12-18 months contract position, onsite.

Qualifications:

  • Bachelor's degree or equivalent
  • Generally requires minimal to no prior relevant work experience
  • Demonstrated knowledge of analytical equipment and instrumentation and working in a GMP environment is helpful
  • Proven skills in coordinating and leading day-to-day tasks and working in collaboration to accomplish deadlines and objectives

Essential Duties and Responsibilities:

  • First shift hours: Mon-Friday, 8am - 4pm
  • Conduct routine preparations for stability, raw materials, in-process, microbiology/cleaning validation program, and other requested testing according to Standard Operating Procedures (SOP) and Analytical Methods in accordance with current Good Manufacturing Practices (cGMPs) and regulatory requirements
  • Complete projects with supervision and have a clear understanding of Good Laboratory Practices (GLPs), cGMPs, and other regulatory requirements
  • Ability to exercise judgment and appropriately raise issues to QC management
  • Key focus will be preparing solutions (mobile phase, diluent, etc.) and standard/sample preparations
  • Outstanding interpersonal skills, both written and oral, and encouraged to collaborate with other analysts and management
  • Ensure equipment is performing well and communicate and take appropriate action as necessary
  • Required to follow good documentation practices
  • Work cross-functionally to complete projects and testing

Job Posting Description
The world's most revolutionary biopharma companies are partnering to advance the next frontier of medicine. The company continues to invest in capacity and expansion of its Colorado operations. Join a team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life-changing, lifesaving medicines.

Candidates must provide their phone number. Job reference number is A5186.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: NETSO
  • Position Id: A5186
  • Posted 2 days ago
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