Quality Assurance Associate; Night Shift
Job in
Holly Springs, Wake County, North Carolina, 27540, USA
Listed on 2026-02-19
Listing for:
Planet Pharma
Full Time
position Listed on 2026-02-19
Job specializations:
-
Quality Assurance - QA/QC
Quality Technician/ Inspector, Quality Control / Manager -
Manufacturing / Production
Job Description & How to Apply Below
Job Details:
The role will support the inspection, sampling, and testing of raw materials that are received at the North Carolina (NC) site. This role will ensure that raw materials received for use in our cGMP manufacturing plants meet all specification requirements and master inspections characteristics required for use in our manufacturing process. This role will also demonstrate leadership skills in support of scheduling, coordination, and staff training.
There will be opportunities to advance Quality learning through additional responsibilities and training.
Primary Responsibilities of the Role Include:
- Inspect materials including biobags, tubing, filters, and other components to ensure all inspection-related specification requirements and master inspections characteristics are met.
- Remove samples from containers of medias and other chemicals to facilitate the testing of samples.
- Use RAMAN technology with Tru Scan equipment to identify chemicals.
- Ensure that inspection & sampling results are complete and detailed according to written procedures and cGMP requirements.
- Responsible for accurately documenting inspection, sample, and test results in systems.
- Responsible for ensuring that characteristics that could potentially impact product quality are assessed according to procedures.
- Ability to determine the color of components match required attributes.
- Support inspection readiness activities.
- Supports Continual Improvement initiatives, programs and projects.
- Assist area management with the prioritization and scheduling of tasks.
- Serve as a trainer in tasks associated with raw material inspections, samples, and testing.
- Own controlled documents for the area including SOPs and FORMs.
- Initiate and own deviation records and CAPAs associated with events and projects in ANCs raw material inspections, samples, and testing areas.
- Provide QA oversight to Warehouse and ensure they are adhering to GMP regulations.
Position Requirements
10+ Years
work experience
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