Technician I, Manufacturing QA (3rd Shift Sun-Thurs)

The Manufacturing QA Technician will perform sampling and visual inspection of finished and in-process materials per operating procedures and the electronic batch record. Uses programs (e.g., POMS and SAP) to evaluate in-process data to determine acceptable quality limits and product release requirements. Supports a quality-focused environment and drives for excellence.

Responsibilities:
- Perform visual inspection of finished and in-process materials, classify defects, and determine test disposition to ensure products meet acceptable quality limits based on FDA regulations.
- Enter in-process inspection results for Acceptable Quality Limits and defect recognition in manufacturing systems (e.g., SAP, POMS, Laboratory Information Management System).
- Maintain accurate documentation in compliance with Good Documentation Practice.
- Manage quality sampling across multiple production lines per the production schedule.
- Execute assigned tasks with minimal supervision; seek guidance when issues are beyond training/scope.
- Elevate safety, quality, technical, and operating issues in a timely manner.
- Support improvement opportunities in documentation, procedures, processes, and equipment via cross-functional teams.
- Collaborate to maintain a positive atmosphere and working relationships.

Qualifications:
- High School Diploma required.
- 1–2 years experience conducting quality inspections in a pharmaceutical setting (preferred).
- 1–2 years experience in a manufacturing/packaging environment (preferred).
- Ability to support 5S, safety, and compliance activities/walk-throughs.
- Knowledge of cGMP requirements/procedures affecting pharmaceutical products (preferred).
- Basic computer skills; ability to learn new programs.
- Stand 8–12 hours/day; lift up to 25 lbs.
- Additional hours may be required.
- Communicate clearly and effectively.

Shift: 3rd shift (Sunday–Thursday, 11pm–7am).