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Rentschler Biopharma SE Verified 17h ago

Quality Control Analyst II, Release & Stability Testing (3rd Shift - Contract)

Milford, MA, United States On-site

$81,120 a year
Pay$81,120
TypeContract
Work settingOn-site
Verified listing

JobFig found this opening at its original source and checks that it remains available.

About the role

The Quality Control Analyst II, Release and Stability Testing is responsible for the cGMP analytical testing of stability samples and evaluation of data to ensure compliance with analytical methods, stability protocols, client criteria, Good Laboratory Practices (GLP) and Good Manufacturing Practices (cGMP). They work independently with minimal supervision ensuring stability tests are performed promptly within predefined testing windows. The Quality Control Analyst II, Release and Stability Testing, ensures all work performed strictly adheres to cGMP, SOPs, and protocols. They collaborate with QC team members and cross functional teams for timely resolution of quality issues to achieve project goals. They are responsible for identifying and resolving problems of diverse scope in which analysis of data requires evaluation of identifiable factors based on biochemical knowledge and background. Rentschler Biopharma, Inc is committed to fair and equitable compensation practices. The base pay range listed for this position is the anticipated annual base salary range the organization reasonably, and in good faith, expects to pay for this position at this time. Actual compensation is determined based on several factors that may include seniority, education, training, relevant experience, relevant certifications, geography of work location, job responsibilities, or other application factors permissible by law. The salary pay range is subject to change and may be modified at any time.

What you'll bring

  • Bachelor's Degree in Life Sciences discipline
  • Minimum 3+ years’ experience in a cGMP analytical lab environment
  • Must have the ability and skill to perform the detailed job requirements competently, safely, accurately, and proficiently
  • Self-starting motivated person who possesses excellent time management, the ability to adapt to change and organizational skills
  • Able to communicate, receive, and understand information and ideas with diverse groups of people in a collaborative, comprehensible and reasonable manner
  • Able to use and learn standard office equipment and technology with proficiency
  • Experience in Empower chromatography software