Manufacturing Technician II - Inspection; PFS Nights

Position: Manufacturing Technician II - Inspection (PFS 2 Nights)
.Manufacturing Technician II
- Inspection (PFS 2 Nights) page is loaded## Manufacturing Technician II
- Inspection (PFS 2 Nights) locations: USA - OH
- West Chester time type:
Full time posted on:
Posted Yesterday job requisition : R-106992A 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

The Manufacturing Technician II reports to a Supervisor/Manager, Manufacturing and works in Controlled/Non-Classified areas, supporting Inspection operations. The Technician performs a variety of tasks including operating inspection equipment, performing visual/cosmetic/physical inspection, line clearances, OEE data collection, and completing batch record entries per cGMPs.#
** Job Responsibilities
**** Operations
* ** Perform the duties of operating assigned inspection machinery: service automated inspection equipment, monitor equipment status, reintroduce materials, manually palletize inspected materials, and ensure smooth product flow.
* Perform manual visual, cosmetic, and physical inspection of material; promptly escalate concerns to Lead and Supervisor/Manager as needed.
* Start-up equipment, make minor adjustments, remove jams, perform minor troubleshooting, and perform minor assembly/disassembly for cleaning purposes.
* Use material handling equipment such as motorized and manual pallet jacks and non-motorized lifts.
* Transfer materials in and out of cold rooms as needed.
* Perform cleaning, housekeeping, and line clearance activities for assigned areas to maintain a cGMP environment.
* Support lean activities and process improvement work including 5S and problem-solving.
* Identify and propose process improvements while maintaining quality and cGMP compliance.
* Perform inventory control using SAP.
** Documentation & Compliance
*** Perform batch record and GMP documentation entries, including mathematical computations; maintain records and logs as required.
* Access and print SOPs and forms via ECMS as required.
* Use process documents including SOPs, forms, and batch records to guide work; report discrepancies to supervisor.
* Follow job-related safety procedures including PPEs, LOTO, ergonomics, material handling, chemical/waste/spill controls, and human safety.
** Training & Development
*** Acquire and maintain all required certifications and qualifications for the assigned work area, including visual inspection qualification and cold room training.
* Cross-train and support other work areas as needed.
* Attend and actively participate in daily Tier meetings.#
** Experience & Education
**** Minimum Qualifications
*** Prior experience in a regulated manufacturing environment.
* Ability to detect visual defects and perform repetitive inspection tasks with sustained accuracy.
* Working knowledge of product security controls and material handling equipment.
* Demonstrated documentation and data entry skills, including accurate completion of batch records and logbooks.
* Basic mathematical skills, including the ability to perform routine calculations (e.g., weights, measures, conversions).
* Ability to effectively read, write, speak, and understand English to interpret SOPs, batch records, and work instructions.
* Ability to follow written procedures and work instructions with minimal supervision, escalating issues as needed.
* Basic problem-solving skills and the ability to identify deviations or inconsistencies in processes or documentation.
* 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.
* Prior inspection experience.
* 1+ years of experience in a pharmaceutical, biotechnology, or cGMP-regulated manufacturing environment.
* Working knowledge of cGMP principles, including documentation practices, safety procedures, and compliance expectations.
* Familiarity with defect classification, batch documentation, and GDP/GMP practices.
* Working knowledge of Microsoft applications, SAP and/or Veeva Vault.
* Experience working in a lean manufacturing environment.#
** Physical & Work Environment
*** This role is primarily a non-Sedentary role. This can include climbing, kneeling, repetitive…