Analyst, QC Micro – Lab

Resilience; Olde West Chester (OH); On-site; USD 33,000 - 48,000; Full time

Benefits offered by this job

Annual cash bonus

401(k) plan with generous match

Excellent healthcare benefits

Paid vacation and holidays

Tuition reimbursement

Caregiver support

Job summary

Resilience, a technology-focused biomanufacturing company, seeks an Analyst, QC Micro to perform microbiological testing and support the site’s quality control program with strict cGMP adherence.

You will conduct routine sampling, verify materials, analyze data trends, write and update SOPs, and contribute to CAPA and audits while maintaining accurate records and regulatory readiness on site.

Qualifications

• Experience performing microbiological testing or analytical laboratory work in a regulated or cGMP environment.
• Ability to analyze laboratory data, identify trends or deviations, and communicate observations to supervisors.
• Familiarity with cGMP documentation and SOP compliance.

Responsibilities

• Perform routine sampling, in-process testing, autoclaving, and parts washing per cGMP.
• Monitor equipment and troubleshoot issues; implement fixes.
• Write, review, and revise SOPs and work instructions for manufacturing systems.

Skills

Microbio testing

Analytical lab work

cGMP knowledge

Data analysis

Education

Bachelor’s in biology or microbiology

Tools

Laboratory instrumentation

MS Word / MS Office

Job description

A career at Resilience is more than just a job – it’s an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more information, please visit www.resilience.com

Brief Job Description

The Analyst, QC Micro – Lab performs microbiological testing and quality control activities in support of the site’s microbiological control program.

Job Responsibilities

Core Responsibilities

• Perform routine sampling, utility testing, in-process testing, autoclaving, and parts washing in accordance with cGMP
• Perform visual inspections and verify materials for correct components, quantities, and characteristics
• Monitor equipment and systems for performance and problem indicators; troubleshoot and implement temporary and permanent fixes
• Maintain accurate records and archived documentation (laboratory notebooks, logbooks, quality records, sample receipts) per good documentation practices, including periodic logbook reviews
• Write, review, and revise SOPs and work instructions for cGMP manufacturing, equipment, systems, and facilities
• Analyze data trends to identify root causes, collect and report quality metrics, and recommend corrective actions
• Audit SOPs and work instructions to ensure compliance with regulatory requirements; elevate issues outside of SOPs to supervisor or manager
• Interact with regulatory agency personnel during audits and inspections
• Contribute to compliance, CAPA, and process improvement activities
• Train others on systems, equipment, procedures, and SOPs
• Serve as an SME cross-functionally; answer compliance and process questions and coordinate with support groups
• Communicate policies, procedures, and operational information across employee and management levels
• Use CMMS to manage logistics

Experience & Education

Minimum Qualifications

• Experience performing microbiological testing or analytical laboratory work in a regulated or cGMP environment
• Ability to independently apply laboratory skills within own job area, drawing on microbiological knowledge and cGMP experience
• Ability to analyze laboratory data, identify trends or deviations, and raise observations and recommendations to supervisor
• Working knowledge of cGMP documentation requirements (logbook practices, deviation identification, SOP compliance)
• Ability to prepare clear, accurate technical documentation consistent with cGMP requirements

Preferred Qualifications

• Bachelor’s degree in biology, microbiology, or a related discipline
• 1+ years of experience in a regulated or cGMP laboratory environment
• Proficiency with laboratory instrumentation
• Working knowledge of cGXP requirements and familiarity with production operations
• Proficiency with MS Word and Microsoft Office applications
• Knowledge of cGMPs and FDA regulations

Physical & Work Environment

This is primarily a non-sedentary role that can include climbing, kneeling, standing, repetitive motion, temperature changes, exerting up to100pounds of force to move objects, and potential exposure to area chemicals requiring handling precautions per SOP. Use of personal protective equipment, which can include respirators, Personal Air Purifying Respirators[PAPR], gowns, gloves, face protection, other barrier equipment, etc. Using a computer keyboard, mouse, or other electronic/laboratory device; interpreting sounds and associated meanings at volume levels consistent with interpersonal or group conversations; interpreting letters and numbers when viewed on a computer screen, monitor, reports and other documents; identifying and distinguishing colors. All employees are expected to adhere to the Quality Management System established in the Quality Manual, Quality Policy, Standard Operating Procedures, Current Good Manufacturing Practices, and any other applicable regulations and standards to the duties within their role.

Work Schedule

Monday - Friday with some on - call support. The work schedule listed reflects the employee’s expected schedule at the time of hire. The Company reserves the right to modify work schedules at any time, including a request to work overtime, with or without notice, based on business needs, operational requirements, or other considerations. Nothing in this description creates a guarantee of specific hours, days, or shift assignments. This role requires the ability to provide 24/7 on‑call support as needed. Sponsorship or support for work authorization, including visas, is not available for this position.

Resilience is an Equal Employment Opportunity Employer.

Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws.

Requests for reasonable accommodation can be made at any stage of the recruitment process.

Resilience offers employees a robust total rewards program including:

• an annual cash bonus program
• a 401(k) plan with a generous company match
• our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision)
• family building benefits
• life and disability insurance
• paid vacation
• paid holidays
• other paid leaves of absence
• tuition reimbursement
• support for caregiving needs

Our target base pay hiring range for this position is $24.00 - $34.50 per hour. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate’s geographical location, relevant experience, qualifications, skills and knowledge.

RESILIENCE is a first-of-its-kind manufacturing and technology company dedicated to broadening access to complex medicines and protecting biopharmaceutical supply chains against disruption. Founded in2020, the company is building a sustainable network of high-tech, end-to-end manufacturing solutions to ensure the medicines of today and tomorrow can be made quickly, safely, and at scale. RESILIENCE will offer the highest quality and regulatory capabilities, and flexible and adaptive facilities to serve partners of all sizes. By continuously advancing the science of biopharmaceutical manufacturing and development, RESILIENCE frees partners to focus on the discoveries that improve patients’ lives.

Please Note – Resilience does not accept unsolicited agency resumes. Resilience will not pay any third-party agency or company that does not have a signed agreement with Resilience.

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