Manufacturing Visual Inspection

We are seeking a detail-oriented Manufacturing Visual Inspection Technician to support drug product manufacturing operations within a multi-product facility. This position is responsible for performing visual inspections, supporting filling and packaging operations, and ensuring products meet established quality and manufacturing standards.

The ideal candidate has experience working in a cGMP-regulated environment, strong attention to detail, and the ability to follow standard operating procedures while maintaining accurate production documentation. This role requires a quality-focused individual who takes pride in accuracy and getting the job done right the first time.

Key Responsibilities

Perform routine manufacturing operations related to drug product visual inspection.

Conduct standard and advanced visual inspections of manufactured products.

Prepare inspection hoods and equipment for production operations.

Perform palletizing, cleaning, and other production support activities.

Assist with drug product filling and packaging operations as needed.

Coordinate logistics and support daily manufacturing activities.

Complete batch records, equipment usage logs, and work order documentation.

Initiate and track work orders and provide support for department projects.

Assist with creating and maintaining training documentation and materials.

Follow all current Good Manufacturing Practices (cGMP) and Good Documentation Practices (cGDP).

Identify and promptly report abnormalities, deviations, and safety concerns.

Maintain clean and organized production areas in accordance with 5S standards.

Support quality investigations, corrective actions, and departmental walkthroughs.

Maintain required training and assist with training other employees once qualified.

Required Qualifications

High school diploma or equivalent.

Minimum of 1 year of experience working in a cGMP-regulated industry.

Strong attention to detail and ability to perform repetitive, quality-focused inspection work.

Ability to read, understand, and follow standard operating procedures (SOPs).

Ability to accurately complete written production documentation in accordance with cGMP standards.

Comfortable using computer-based systems and manufacturing execution systems (MES).

Strong written and verbal communication skills.

Ability to work independently with limited supervision and collaborate within a team environment.

Ability to read clearly and maintain visual focus throughout inspection activities.

Preferred Qualifications

Associate or bachelor's degree.

Vocational training in biotechnology or a related field.

Previous experience with pharmaceutical manufacturing, visual inspection, filling, or packaging operations.

Familiarity with BioMES, batch records, and manufacturing documentation.

Physical & Additional Requirements

Ability to perform physical manufacturing duties as required.

Ability to lift up to 25 lbs., depending on assigned manufacturing activities.

Must successfully pass a vision screening, including visual acuity and color blindness testing, before starting the assignment.

Ability to maintain a clean, organized, and compliant manufacturing environment.

Work Environment & Quality Standards

This position operates in a regulated pharmaceutical manufacturing environment where quality, safety, and compliance are essential. Employees are expected to follow established procedures, maintain accurate documentation, and promptly communicate any deviations or concerns.