Resilience · 3 days ago
Analyst II, QC Microbiology
West Chester, OH
Full-time
Onsite
Entry, Mid Level
$60K/yr - $82K/yr
2+ years expResilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. The Analyst II, QC Microbiology role supports the Microbiology Department by performing quality-related tasks for pharmaceutical products, including testing and documentation on various samples.
BiopharmaBiotechnologyHealth CareLife SciencePharmaceutical
No H1B
Responsibilities
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
Complete required training and may train others
Conduct troubleshooting activities
Gather, organize, and communicate operational information to others
Facilitate team meetings to discuss progress, initiatives, and/or other matters
Actively participates in investigations involving manufacturing process areas, related to QC processes or data, such as sampling, deviations potentially affecting QC results, investigational sampling, and testing
Assist with coordinating activities of support groups
Identifies trends in data in order to provide accurate descriptions, identify root causes, and/or identify solutions or improvements
Demonstrates proficiency on authoring Quality records (Deviations, CAPAs, and Change Controls)
Identify temporary and permanent fixes to address issues
Alert supervisor or manager when problems occur outside of SOPs (Standard Operating Procedures)
Collect, record, and report metrics
Monitor equipment and/or systems for performance and problem indicators
Wear gowning, sterile garments, and PPE (Personal Protective Equipment) as required by specific activities
Consult cross-functionally as an SME (Subject Matter Expert) on systems and/or processes within a functional area
Perform logbook reviews
Lead or participate in process improvement activities and teams to meet strategic goals
Use MAXIMO and/or CMMS (Computerized Maintenance Management System) to manage logistics
Interact with regulatory agency individuals during audits and inspections, when necessary
Author, review, and revise documentation needed for cGMP (Good Manufacturing Practices) manufacturing of commercial product
Attend inter-departmental meetings to discuss matters involving the coordination of multiple departments
Coordinate qualification activities
Perform routine sampling activities on the facility utilities
Recommend compliance resolutions to management
Qualification
Required
Working knowledge of cGXP requirements and a strong familiarity with production operations
Good problem solving skills
Preferred
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
Benefits
Annual cash bonus program
401(k) plan with a generous company match
Great healthcare (including medical, dental and vision)
Family building benefits
Life and disability insurance
Flexible time off
Paid holidays
Other paid leaves of absence
Tuition reimbursement
Support for caregiving needs
Company
Resilience
Resilience is a biomanufacturing company that provides access to complex medicines and protects biopharmaceutical supply chains.
1001-5000 employees
Funding
Current Stage
Late StageTotal Funding
$3.36BKey Investors
Oak Hill AdvisorsAdministration for Strategic Preparedness and ResponseMubadala
2025-10-29Debt Financing· $825M
2024-10-03Grant· $17.5M
2023-03-24Debt Financing· $410M
Leadership Team
William Marth
President and CEO
Susan Billings
Chief Commercial Officer (CCO)
Recent News
Help Net Security
2025-11-11
2025-11-05
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