Manufacturing Technician II - Inspection

Resilience•West Chester, OH

1d•$22 - $32

About The Position

The Manufacturing Technician II reports to a Supervisor/Manager, Manufacturing and works in Controlled/Non-Classified areas, supporting Inspection operations. The role performs tasks including operating inspection equipment, performing visual, cosmetic, and physical inspections, conducting line clearances, collecting OEE data, and completing batch record entries in accordance with cGMPs. The technician operates and services assigned inspection machinery, monitors equipment, supports product flow, inspects materials manually, performs minor equipment adjustments and troubleshooting, and handles materials using pallet jacks and lifts. The role also includes cleaning and housekeeping, line clearance, inventory control using SAP, process improvement activities, documentation, and compliance with safety and quality procedures. The technician maintains required qualifications, cross-trains, supports other work areas, and participates in daily Tier 1 meetings. This is a primarily non-sedentary role involving activities such as climbing, kneeling, repetitive motion, temperature changes, and exerting up to 100 pounds of force to move objects. The position requires visual acuity, use of personal protective equipment, participation in an occupational health program, and passing an eye exam during onboarding. The work schedule is subject to change, and overtime may be requested based on business needs. Work authorization or visa sponsorship is not available.

Requirements

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 routine calculations involving weights, measures, and 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 and escalate issues as needed.
Basic problem-solving skills and ability to identify process or documentation deviations and inconsistencies.
Ability to work effectively as part of a team in a fast-paced production environment.
Ability to pass an eye exam during onboarding.
Ability to meet the physical demands of a primarily non-sedentary role, including climbing, kneeling, repetitive motion, temperature changes, and exerting up to 100 pounds of force to move objects.
Ability to use required personal protective equipment and participate in an occupational health program, which may include medical assessment, surveillance, vaccination, and testing.
Adherence to the Quality Management System, Quality Manual, Quality Policy, SOPs, cGMPs, and other applicable regulations and standards.

Nice To Haves

High school graduate, vocational school graduate, or equivalent.
Prior inspection experience.
At least 1 year of experience in pharmaceutical, biotechnology, or cGMP-regulated manufacturing.
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.

Responsibilities

Operate assigned inspection machinery, service automated inspection equipment, monitor equipment status, reintroduce materials, manually palletize inspected materials, and support smooth product flow.
Perform manual visual, cosmetic, and physical inspections of materials and escalate concerns to the Lead and Supervisor/Manager as needed.
Start up equipment, make minor adjustments, remove jams, perform minor troubleshooting, and conduct minor assembly or disassembly for cleaning.
Use motorized and manual pallet jacks and non-motorized lifts to handle materials.
Transfer materials in and out of cold rooms as needed.
Perform cleaning, housekeeping, and line clearance activities 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.
Complete batch record and GMP documentation entries, including mathematical computations, and maintain required records and logs.
Access and print SOPs and forms through ECMS as required.
Use SOPs, forms, batch records, and other process documents to guide work and report discrepancies to a supervisor.
Follow job-related safety procedures, including PPE, LOTO, ergonomics, material handling, chemical, waste, spill-control, and human-safety procedures.
Acquire and maintain required work-area certifications and qualifications, including visual inspection qualification and cold room training.
Cross-train and support other work areas as needed.
Attend and actively participate in daily Tier 1 meetings.