QC Microbiology Associate | 10-Hour GMP Lab Shift

BioSpace

West Greenwich (RI)

On-site

USD 60,000 - 90,000

Full time

13 days ago
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Job summary

Amgen is seeking an Associate Quality Control specialist in Rhode Island to perform microbiology and analytical testing, manage samples and data, and operate lab instrumentation in a dynamic team setting.

The role requires strong GxP experience, effective communication, and the ability to generate precise documentation while maintaining strict compliance with safety and regulatory standards. Expect a 10-hour shift schedule and ongoing professional development.

Qualifications

  • Experience in a regulated biotechnology/pharmaceutical lab environment.
  • Written and oral communication skills for quality/compliance documents.
  • Flexibility to support business needs and projects.

Responsibilities

  • Perform analytical testing, characterization, sample and data management.
  • Collect and handle samples to support GMP operations.
  • Test and review data for compendial and non-compendial methods.
  • Generate complete, accurate laboratory documentation using electronic systems.
  • Operate and maintain specialized laboratory equipment and instrumentation.
  • Participate in investigations and audits as necessary.
  • Maintain safety guidelines, cGMPs and regulatory compliance.
  • Maintain training compliance and proficiency.

Skills

Microbiology testing
GxP experience
Communication skills
Electronic systems (LIMS/Trackwise)
Project management
Lean Manufacturing / 5S

Education

High school/GED + 2 years experience
Associates + 6 months experience
Bachelor's degree

Tools

LIMS
LMES
TrackWise

Job description

Amgen is seeking an Associate Quality Control specialist in Rhode Island to perform microbiology and analytical testing, manage samples and data, and operate lab instrumentation in a dynamic team setting.

The role requires strong GxP experience, effective communication, and the ability to generate precise documentation while maintaining strict compliance with safety and regulatory standards. Expect a 10-hour shift schedule and ongoing professional development.

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