Maintenance Technician IV, Lead - Sterile Operations (Night Shift

Position: Maintenance Technician IV, Lead - Sterile Operations (Night Shift)
## Maintenance Technician IV, Lead
- Sterile Operations (Night Shift)
Apply locations:
USA - OH
- West Chester time type:
Full time posted on:
Posted 2 Days Agojob requisition :
R-106946A 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
** Brief

Job Description
** The Manufacturing Technician IV, Lead supports Filling operations. The position leads complex filling batch activities on the manufacturing floor, serves as a technical resource for the team, performs advanced-level documentation review, and resolves technical production issues.
** Job Responsibilities
**** Operations
* ** Lead and monitor process execution activities to ensure successful operations on the production floor.
* Serve as a technical resource for the team; resolve complex production-related issues including batch setup, execution, technical interventions, documentation, equipment operations, and safety/quality.
* Provide support to production technicians and mechanical technicians.
* Apply strong organizational and problem-solving skills to make independent decisions and provide guidance to team members on daily operational activities.
* Perform and execute filter integrity testing as needed per SOP.
* Perform technician tasks as required, including start-up, equipment operation, batch execution, material handling, and cleaning.
* Assemble, disassemble, and sanitize various Filling equipment.
* Assist technical staff with preventive maintenance procedures, as required.
* Manage inventory control and reconciliation activities using SAP.
** Documentation & Compliance
*** Perform advanced-level batch record and GMP documentation entries on the production floor, including complex or non-routine documentation; provide guidance to team members on documentation accuracy.
** Training & Development
*** Serve as a technical resource for the team, providing subject-matter support to production and mechanical technicians.
* Act as a certified OJT trainer on assigned equipment and process tasks, training and supporting team members.
* Support lean activities such as performing 5S and participating in problem-solving and CI projects.
* Attend and actively participate in daily tier meetings.
** Minimum Qualifications
*** Significant experience in a pharmaceutical, biotechnology, or cGMP-regulated manufacturing environment.
* Advanced knowledge of cGMP requirements, regulatory expectations, and quality systems, including deviations, CAPAs, audits, and inspections.
* Demonstrated ability to work independently and resourcefully to resolve complex production issues and provide guidance to team members.
* Ability to effectively read, write, speak, and understand English to communicate complex technical information cross-functionally.
* Exceptional attention to detail with proven ability to review and ensure accuracy of critical documentation and records.
* Strong mathematical, analytical, and problem-solving skills, with the ability to interpret data, identify trends, and drive solutions.
* Proven ability to support investigations, root cause analysis, and implementation of corrective and preventive actions (CAPAs).
* Experience providing on-the-job training to peers while fostering a culture of compliance and continuous improvement.
* Ability to manage own priorities, make informed decisions under pressure, and ensure production goals are met while maintaining regulatory compliance.
* Experience supporting audits and regulatory inspections, including interacting with internal and external auditors.
* Ability to work effectively as part of a team in a fast-paced production environment.
** Preferred Qualifications
*** High school graduate, vocational school graduate, or equivalent.
* 4+ years of experience in a pharmaceutical, biotechnology, or cGMP-regulated manufacturing environment.
* Experience working in a lean manufacturing…