Resilience

Analyst II, QC Microbiology

USA - OH - West Chester · Mid · Contract

Sponsorship not specified$60k-$86kDetected 9 days ago

Process ImprovementGMPProblem Solving

About the role

Read SOPs (Standard Operating Procedures) and excerpts from technical documentation.
Write, review, and revise SOPs (Standard Operating Procedures) and/or work instructions for cGMP (Good Manufacturing Practices) manufacturing of commercial product.
Gather, organize, and communicate operational information to others.

Assist with coordinating activities of support groups.
Use MAXIMO and/or CMMS (Computerized Maintenance Management System) to manage logistics.
Sponsorship or support for work authorization, including visas, is not available for this position.

Working knowledge of cGXP requirements and a strong familiarity with production operations.
Complete required training and may train others.
Demonstrates proficiency on authoring Quality records (Deviations, CAPAs, and Change Controls).

Bachelor's degree in biology, microbiology, or related discipline.
At least 2 year of laboratory experience in pharmaceutical industry.
Prior experience supporting microbiological testing in a sterile pharmaceutical operation environment.
This position may also include the following conditions:
This role is primarily non-sedentary.
May include but not limited to standing, walking, repetitive motion, and chemical usage.
The items described here are representative of those that must be met successfully to perform the essential functions of this job.
Resilience is an Equal Employment Opportunity Employer.

Our target base pay hiring range for this position is $60,000.00 - $86,250.00 per year.

Sponsorship or support for work authorization, including visas, is not available for this position.

This listing is sourced directly from Resilience's careers page and normalized into a canonical job model.