Quality Technician II, Aseptic Control (Day Shift - 12-Hour Rotating Schedule)

Resilience US

Olde West Chester (OH)

On-site

USD 42,000 - 64,000

Full time

2 days ago
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Benefits offered by this job

Annual cash bonus
401(k) plan with match

Job summary

Resilience US is seeking a Quality Technician II, QC Micro - Aseptic Control at the WCH site. You will perform environmental monitoring and microbial sampling in classified and non-classified areas, including Class 100/ISO 5 aseptic environments, supporting sterile manufacturing operations.

Under cGMP, you will collect and analyze samples, maintain documentation, and ensure activities comply with SOPs. The role involves hands-on lab work, data entry, and training new technicians; day shift

Qualifications

  • Ability to follow written procedures with minimal supervision.
  • Strong attention to detail and record-keeping.
  • English reading, writing and speaking proficiency in the workplace.

Responsibilities

  • Document activities, actions, and results per SOPs; maintain complete records.
  • Perform visual inspections and routine sampling using EM System; data entry.
  • Follow SOPs and cGMP requirements in all lab duties.
  • Maintain compliant work area and equipment; report deviations.
  • Audit SOPs and work instructions; suggest improvements.
  • Assist in training new technicians.

Skills

SOP adherence
Documentation
English fluency

Education

High school diploma
Vocational training

Tools

MODA
LIMS
Novatek
Microsoft 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

The Quality Technician II, QC Micro - Aseptic Control performs environmental monitoring and microbial sampling activities in classified and non-classified areas, including Class 100/ISO 5 aseptic environments, in support of sterile manufacturing operations at the WCH site. Working under established procedures and SOPs, this role collects and analyzes environmental samples, maintains accurate cGMP documentation, and ensures laboratory activities are conducted in a state of compliance.

Job Responsibilities
Core Responsibilities
  • Document activities, actions, and results per documentation practices; read SOPs and technical documentation as required, and maintain accurate, complete records (e.g., laboratory notebooks, quality records, sample receipts).
  • Perform visual inspections and routine sampling activities, including using the Environmental Monitoring System to collect and analyze samples, with associated data entry.
  • Follow SOPs, control documents, and work instructions; perform laboratory duties consistent with cGMP requirements.
  • Maintain work area and equipment in a state of compliance with applicable SOPs and cGMP requirements; report deviations or non-conformances to supervisor.
  • Audit SOPs and work instructions; recommend and initiate activities to keep area and equipment in a state of compliance.
  • Support the training of new technicians
Experience & Education
Minimum Qualifications
  • Ability to follow written procedures, SOPs and work instructions with minimal supervision, escalating issues as needed.
  • Strong attention to detail, with the ability to keep accurate records and perform mathematical calculations.
  • Ability to effectively read, write, speak, and follow instructions English.
Preferred Qualifications
  • High school graduate, vocational school graduate, or equivalent.
  • 1+ years of experience in a pharmaceutical, biotechnology, or cGMP-regulated manufacturing environment.
  • Working knowledge of Microsoft applications, MODA, LIMS, Novatek, or equivalent sampling and testing software.
  • Experience working in a LEAN manufacturing environment.
  • Knowledge of cGMPs and FDA policies/procedures.
Physical & Work Environment

This is primarily a non-Sedentary role that can include climbing, kneeling, standing, repetitive motion, temperature changes, exerting up to 100 pounds 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

Day shift: 6AM - 6:30PM, 12-hour 2/2/3 schedule

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 and our benefits

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