More jobs:
Inspector/Labeler
Job in
Lexington, Fayette County, Kentucky, 40598, USA
Listed on 2026-01-12
Listing for:
Piramal
Full Time
position Listed on 2026-01-12
Job specializations:
-
Manufacturing / Production
Quality Engineering -
Quality Assurance - QA/QC
Quality Engineering
Job Description & How to Apply Below
Business:
Pharma Solutions
Department:
Operations
Location:
Lexington
Reporting to the Process Technician Supervisor, the primary purpose of the Inspector/Labeler role is to perform visual inspection, labeling, and packaging activities for finished product, according to Good Manufacturing Practices (GMP) and site specific Standard Operating Procedures (SOP).
Reporting StructureThis position reports to the Process Technician Supervisor.
ShiftDays
Key Responsibilities- Preparation of Line clearances for inspection, labeling and packaging processes.
- Clean and disinfect any inspection/labeling equipment and rooms, preparing of rooms and equipment.
- Cleaning of SS trays post inspection.
- Maintain inspection, labeling and packaging areas clean and organize at all times.
- Inspection of both liquids and freeze dried products.
- Labeling of both liquids and freeze dried products.
- Packaging of both liquids and freeze dried products.
- Request QA AQL.
- Transfer Materials and/or components from in and out of the production area and back into the WHS.
- Daily verification of room temperature and humidity chart recorders.
- Read, understand, and comply with Good Manufacturing Practices and Standard Operating Procedures.
- Maintain and review completed production documentation (batch records, log books, etc.) for quality and cGMP compliance.
- Initiate appropriate action when process deviations occur.
- Other duties as assigned by production supervisor.
- High School education or equivalent
- Minimum 1-year experience working with a manufacturing/industrial environment, pharmaceutical manufacturing preferred
- Experience performing visual quality checks on products within a manufacturing environment
- Prior knowledge and/or ability to understand and follow job related regulatory requirements (cGMP, OSHA, FDA)
- Keen attention to detail and ability to read, interpret and follow written instructions
- Team player committed to quality and working effectively with others
- Track record of consistent attendance and overall reliability
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