Manufacturing Technician II - Sterile Filling

## Manufacturing Technician II
- Sterile Filling Apply:
USA - OH
- West Chester:
Full time:
Posted Today:
R-107229A 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.comJob Description The Manufacturing Technician II, In-Line Inspector supports sterile filling inspection operations, working in various Controlled/Non-Classified areas. The Technician operates automated and manual inspection equipment; performs visual, cosmetic, and physical inspection of materials; executes line clearances; and completes batch record entries. The role also supports improvement activities such as 5S, problem-solving, Kaizen events, and manual data collection, all in accordance with cGMPs.#

** Job Responsibilities
**** Operations
* ** Accountable for the outgoing quality level of inspected product; perform manual visual, cosmetic, and physical inspection of material, promptly escalating concerns to the Lead and Manager/Supervisor. Must obtain and maintain visual inspection qualification.
* Operate assigned machinery, including servicing automated inspection equipment, monitoring equipment status, reintroducing materials, manually palletizing inspected materials, and assuring a smooth flow of product.
* Start up equipment, make minor adjustments to machinery, remove jams, and perform minor troubleshooting and assembly/disassembly for cleaning.
* Use material handling equipment such as motorized and manual pallet jacks and non-motorized lifts.
* Perform cleaning, housekeeping and line clearance activities for assigned areas as required to maintain a cGMP environment.
* Apply knowledge of product security controls.
* Perform work in accordance with SOPs, cGMPs, and OSHA-compliant safety procedures, maintaining familiarity with job-related hazards and controls (PPE, ergonomics, LOTO, human/material/waste/chemical handling, and spill control) and area chemical Safety Data Sheets. Report all discrepancies to the process facilitator.
* Print SOPs and forms via ECMS.
* Support lean and process-improvement activities, including 5S, problem-solving, and manual tracking of OEE performance data.
* Review operational SOPs, forms, and batch records for accuracy, and suggest process improvements while maintaining quality and cGMP compliance.
** Documentation & Compliance
*** Perform batch record and GMP documentation entries; maintain records and logs as required, including mathematical computation where needed.
* Perform inventory control, reconciliation, and inventory movements using SAP in a limited role (e.g., moving items between storage locations and goods-issuing to process orders).
** Training & Development
*** Acquire and maintain all required certifications and qualifications for the assigned work area, including cold room training/access to transfer materials in and out of the cold rooms.
* Cross-train and support other work areas as needed.# #
** Experience & Education
**** Minimum Qualifications
*** Prior experience in a regulated manufacturing environment (e.g., pharmaceutical, biotechnology, medical device, or other GMP-regulated industry) is preferred. Experience in manufacturing, quality, or visual inspection is highly desirable.
* Ability to effectively read, write, speak, and understand English to accurately interpret and follow Standard Operating Procedures (SOPs), batch records, work instructions, specifications, and other controlled documentation.
* Basic…