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Resilience

Biologics and sterile injectables CDMO

Senior Analyst, QC Micro – Aseptic - Aseptic Control

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeWest Chester Township, OH, USAIn-person

About the Job

Requirements

  • Demonstrated technical expertise in environmental monitoring, aseptic control, or pharmaceutical quality, with the ability to advise the team and drive improvements independently on novel and complex compliance matters.
  • Demonstrated ability to own a technical program end-to-end, set its direction, proactively identify gaps, and drive resolution of complex compliance problems independently.
  • Experience leading technical programs or projects in a regulated pharmaceutical setting and building cross-functional alignment 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 skills.
  • Project management skills.
  • Demonstrated ability to influence the technical decisions and priorities of peers and cross-functional partners through expertise and credibility, without formal authority.

Responsibilities

  • Own environmental monitoring trending (monthly, quarterly, and annual), EMPQ and related document updates, and associated deviations and investigations.
  • Serve as final technical reviewer and approver for environmental monitoring data packages and production and laboratory documentation escalated by the environmental monitoring team, including current Good Manufacturing Practice compliance determinations.
  • Respond to compliance and process questions, including questions 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 environmental monitoring program, develop recommendations, and drive cross-functional alignment around solutions.
  • Develop and deliver technical training and qualification content for environmental monitoring 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 environmental monitoring team on compliance questions outside established procedures.
  • Fill in for the direct manager on technical and compliance matters as needed.
  • Adhere to the Quality Management System established in the Quality Manual, Quality Policy, Standard Operating Procedures, Current Good Manufacturing Practices, and other regulations and standards applicable to the role.

Desired Qualifications

  • Bachelor's degree in engineering, pharmacy, or a related scientific discipline.
  • At least 5 years in pharmaceutical quality control or environmental monitoring.
  • Experience working in a LEAN manufacturing environment.
  • Working knowledge of laboratory data management systems (LDMS) or Veeva, Microsoft applications, SAP, and MODA or equivalent.

About the Company

Resilience

Biologics and sterile injectables CDMO

Resilience is a North American CDMO focused on biologics and sterile drug products. It provides end-to-end services from development through commercial production, including biologics development and drug substance manufacturing, aseptic fill/finish, device assembly, packaging, logistics, regulatory support, and tech transfer, all coordinated via a stage-gate process and a digital quality management system. It differentiates itself with North American-based, integrated biologics and sterile capabilities, a focus on sterile injectables and device assembly, and recent expansion into injectable pen devices for diabetes and obesity medicines. Its goal is to broaden access to complex medicines while protecting North American biopharma supply chains with dependable capacity and strong regulatory support from clinical development to commercial scale.

Company size
1,001-5,000
Company stage
Growth Equity (Venture Capital)
Total funding
$3.2B
Headquarters
Blue Ash, OH
Founded
2020

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