Senior Specialist, Aseptic Control

Resilience US; Olde West Chester (OH); On-site; USD 90,000 - 130,000; Full time

Job summary

Resilience is a technology-focused biomanufacturing company seeking a Senior Analyst, QC Micro - Aseptic. You will own the environmental monitoring program, review data, and advise on complex compliance matters across cross-functional teams.

The role emphasizes independent program ownership, continuous improvement, and proactive regulatory engagement in a fast-paced, regulated setting.

Qualifications

• Experience in environmental monitoring and aseptic control in regulated pharma settings.
• Ability to own a technical program end-to-end and drive improvements.
• Strong communication and leadership skills.
• Experience leading cross-functional projects in a regulated environment.
• Proven ability to influence decisions without formal authority.

Responsibilities

• Own environmental monitoring trending and related documentation.
• Review EM data packages and production/lab docs for cGMP compliance.
• Respond to regulatory and compliance inquiries.
• Develop and maintain EM program in regulatory compliance.
• Lead investigations, impact assessments, and mitigations.
• Represent EM on deviation/change management committees.
• Lead process improvement activities.
• Identify EM program gaps and drive cross-functional solutions.

Skills

Environmental monitoring

Aseptic control

GMP/compliance mindset

Cross-functional collaboration

Technical problem solving

Education

Bachelor's degree in engineering/science

5+ years pharma QC or EM experience

Tools

LDMS or Veeva

SAP

MODA or equivalent

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

The Senior Analyst, QC Micro - Aseptic serves as the technical authority for the site environmental monitoring and aseptic control program, independently owning EM program integrity, proactively driving improvement across the program, and advising the team and cross-functional partners on complex compliance matters without being directed to do so.

Job Responsibilities

Environmental Monitoring Execution & Data Review

• Own environmental monitoring trending (monthly, quarterly, annual), EMPQ and related document updates, and associated deviations and investigations
• Serve as final technical reviewer and approver for EM data packages and for production and lab documentation escalated by the EM team, including cGMP compliance determinations
• Respond to compliance and process questions, including from regulatory agencies
• Develop and maintain the environmental monitoring program in regulatory compliance
• Lead complex investigations, impact assessments, and mitigations
• Represent the Aseptic Control Team on deviation and change management committees
• Lead process improvement activities
• Proactively identify gaps in the EM program, develop recommendations, and drive cross-functional alignment around solutions

Training & Team Support

• Develop and deliver technical training and qualification content for EM and aseptic control personnel, and assess ongoing competency
• Coach analysts and technicians on data interpretation, investigation methodology, and compliance decision-making
• Serve as the technical escalation point for the EM team on compliance questions falling outside established procedures
• Fill in for direct manager on technical and compliance matters as needed

Experience & Education

Minimum Requirements

• Demonstrated technical expertise in environmental monitoring, aseptic control, or pharmaceutical quality; able to advise the team and drive improvements independently, including on novel and complex compliance matters
• Demonstrated ability to own a technical program end-to-end - setting the direction, proactively identifying gaps, and driving resolution of complex compliance problems without being directed to do so
• Experience leading technical programs or projects in a regulated pharmaceutical setting, with cross-functional alignment-building on technical issues
• Strong communication and leadership skills
• Strong mechanical, troubleshooting, and problem-solving abilities
• Ability to direct and participate in cross-functional teams
• Strong technical and scientific writing
• Project management skills
• Demonstrated ability to influence the technical decisions and priorities of peers and cross-functional partners through expertise and credibility, without requiring formal authority

Preferred Requirements

• Bachelor's degree in engineering, pharmacy, or a related scientific discipline
• 5+ years in pharmaceutical QC or environmental monitoring
• Experience working in a LEAN manufacturing environment
• Working knowledge of LDMS or Veeva, Microsoft applications, SAP, and MODA or equivalent

Physical & Work Environment

This is primarily a non-sedentary role.

Use of personal protective equipment, which can include respirators, Personal Air Purifying Respirators [PAPR], gowns, gloves, face protection, other barrier equipment, etc.

Occasional (20-60% of time): sitting, walking, and monitoring other people's work.

Infrequent ( 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; seeing with 20/20 (or better) vision, with or without correction.

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 8 hours, Monday -Thursday 10 hours

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