Manufacturing Technician II - Sterile Filling

## Manufacturing Technician II
- Sterile Filling Apply locations:
USA - OH
- West Chester time type:
Full time posted on:
Posted 2 Days Agojob requisition :
R-107025A 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.comThe Manufacturing Technician II reports to a Supervisor/Manager on the Manufacturing floor, supporting Filling operations. This position requires working in various Controlled/Non-Classified and Classified areas. The Filling Technician operates equipment, performs in-process monitoring, line clearances, OEE data collection, cosmetic inspection, cleaning, and batch record entries in accordance with cGMPs.  #
** Job Responsibilities*
* ** Operations
* ** Perform the duties of operating assigned machinery: servicing filling machines with materials, removing finished materials from machine tables, and assuring smooth product flow.
* Assemble, disassemble, operate, and sanitize various Filling equipment.
* Perform and execute filter integrity testing as needed per SOP.
* Start-up equipment and make minor adjustments as needed.
* Enter data online as required, including SCADA and HMI entries.
* Work with various printing devices, including printing mats.
* Perform cleaning and housekeeping activities for assigned areas as required to maintain a cGMP environment.
* Perform visual and physical checks of in-process and finished materials as requested.
* Understand aseptic behaviors; participate in media fills, including line interventions; maintain basic knowledge of viable and non-viable monitoring equipment.
* Assist mechanical staff with preventive maintenance procedures, as required.
* Assist with executing Validation/Engineering protocols for processes and equipment.
* Support lean activities and process improvement work, such as performing 5S and participating in problem-solving.
* Identify and provide suggestions for process improvement 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 and reconciliation activities using SAP in a limited role.  
** Training & Development
*** Acquire and maintain all required certifications and qualifications for the assigned work area, including aseptic gowning qualification.
* Cross-train and support other work areas as needed.
* Attend and actively participate in daily tier meetings.# # Education & Experience  
** Minimum Qualifications
*** Prior experience in a regulated manufacturing environment.
* Ability to effectively read, write, speak, and understand English to interpret SOPs, batch records, and work instructions.
* 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 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,…