Life Sciences Production Associate – GMP & QC Focus

Cytiva

Logan (UT)

On-site

USD 42,000 - 54,000

Full time

13 days ago
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Job summary

Cytiva, a Danaher operating company, is seeking a Quality & Compliance associate to support GMP training and documentation at our Utah facility.

The role requires a High School Diploma or GED and a couple of years of related manufacturing experience, with strong attention to detail and teamwork. You will work with engineers and supervisors to ensure product quality and regulatory compliance on site in Logan, UT.

Qualifications

  • High School Diploma/GED or local equivalent.
  • Ability to read and follow work policies and procedures, and communicate with team leads and managers.
  • Knowledge of GMPs and Good Documentation Practices.
  • 2 years related manufacturing experience preferred.

Responsibilities

  • Read and follow policies and procedures, complete GMP and quality training.
  • Identify quality or compliance concerns and take immediate corrective action.
  • Ensure product conforms to its specification and maintain documentation and records.

Skills

GMP knowledge
Quality awareness
Team communication

Education

High School Diploma/GED

Tools

MS Office
Teams
Outlook
Word
Excel

Job description

Cytiva, a Danaher operating company, is seeking a Quality & Compliance associate to support GMP training and documentation at our Utah facility.

The role requires a High School Diploma or GED and a couple of years of related manufacturing experience, with strong attention to detail and teamwork. You will work with engineers and supervisors to ensure product quality and regulatory compliance on site in Logan, UT.

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