Manufacturing Technician II - DAP; Dayshift

Position: Manufacturing Technician II - DAP (Dayshift)
.Manufacturing Technician II - DAP (Dayshift) page is loaded## Manufacturing Technician II - DAP (Dayshift) locations: USA - OH - West Chester time type:
Full time posted on:
Posted Yesterday job requisition : R-107211A 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 performs a variety of manufacturing tasks in Controlled/Non-Classified areas in accordance with cGMPs, supporting Packaging operations. Responsibilities include operating packaging equipment, performing in-process monitoring, line clearances, cosmetic inspection, cleaning, and completing batch record entries.#
** Job Responsibilities
**** Operations
* ** Perform the duties of operating assigned machinery: service machines with materials, monitor equipment status, reintroduce materials, manually palletize finished materials, and ensure smooth product flow.
* Start-up machinery including equipment setup, recipe selection, data entry on SCADA and HMI; make minor adjustments and perform critical sensor challenges.
* Perform manual packaging tasks as required including hand packaging and rework of in-process and finished material.
* Operate light material handling equipment (motorized and manual pallet jacks, non-motorized lifts) to safely move, store, or deliver material.
* Perform visual quality inspection and sampling of in-process materials; promptly escalate concerns to Lead and Management as needed.
* Perform minor troubleshooting including clearing minor jams and identifying equipment defects; escalating to the Lead and Management as needed.
* Perform inventory control and reconciliation activities using SAP and WES.
* Perform cleaning, housekeeping, and line clearance activities for assigned areas to maintain a cGMP environment.
** Documentation & Compliance
*** Perform batch record and GMP documentation entries; perform mathematical computations as required.
* Follow job-related safety procedures including PPEs, LOTO, ergonomics, and material/chemical/waste handling, spill controls and human safety.
* Support lean activities and process improvement work including 5S, problem-solving, and manual data collection.
* Execute protocols as required as part of equipment qualification and process validation work.
** Training & Development
*** Provide flexible support to other areas of the Manufacturing Team as needed.
* Acquire and maintain all required certifications and qualifications for the assigned work area.
* Attend and actively participate in daily Tier 0 meetings.#
** Experience & Education
**** Minimum Qualifications
*** Prior experience in a regulated manufacturing environment.
* 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.
* 1+ years of experience in a pharmaceutical, biotechnology, or cGMP-regulated manufacturing environment.
* Experience working in a lean manufacturing environment.
* Working knowledge of cGMP principles, including documentation practices, safety procedures, and compliance expectations.
* Experience working in a lean manufacturing environment.
* Working knowledge of Microsoft applications, SAP and/or Veeva Vault.##
** Physical & Work Environment
*** This role is primarily a non-Sedentary role. This can include climbing, kneeling, repetitive motion, temperature changes, and exerting up to 100 pounds of force to move objects.
* Visual…