Quality Control Technician
AbbVie
3 days ago
On-site
Branchburg, NJ
$21 - $37.80 USD yearly
Operations
Job Description
Performs functions associated with cGMP manufacturing operations within the drug product manufacturing and packaging facility, including performing visual inspection of finished and in-process materials, verifying manufacturing data in the batch record system, and conducting testing on in-process materials. Uses programs such as POMS and SAP to evaluate operating data for acceptable quality limits and product release requirements.
Responsibilities
- Enter test results in manufacturing systems (SAP, POMS, LIMS) and interpret data for conformance with product and material specifications.
- Perform in-process laboratory tests (e.g., Karl Fischer and torque removal testing) per procedure.
- Ensure correct documentation and compliance with GDP requirements.
- Perform visual inspection of finished and in-process materials, classify defects, and determine test disposition.
- Perform test methods to support product/material release and review/verify manufacturing operating settings.
- Suggest improvements based on scientific and good manufacturing practices.
- Maintain a safe work environment for self and others.
- Pursue continual personal development.
- Budget time effectively and participate in team activities/decision-making.
- Collaborate with others to meet business objectives and foster positive relationships.
Qualifications
- High School Diploma required.
- Technical Degree preferred.
- 1–2 years’ experience conducting quality inspections in a pharmaceutical setting required.
- 1–2 years’ laboratory setting experience preferred.
Performs functions associated with cGMP manufacturing operations within the drug product manufacturing and packaging facility, including performing visual inspection of finished and in-process materials, verifying manufacturing data in the batch record system, and conducting testing on in-process materials. Uses programs such as POMS and SAP to evaluate operating data for acceptable quality limits and product release requirements.
Responsibilities
- Enter test results in manufacturing systems (SAP, POMS, LIMS) and interpret data for conformance with product and material specifications.
- Perform in-process laboratory tests (e.g., Karl Fischer and torque removal testing) per procedure.
- Ensure correct documentation and compliance with GDP requirements.
- Perform visual inspection of finished and in-process materials, classify defects, and determine test disposition.
- Perform test methods to support product/material release and review/verify manufacturing operating settings.
- Suggest improvements based on scientific and good manufacturing practices.
- Maintain a safe work environment for self and others.
- Pursue continual personal development.
- Budget time effectively and participate in team activities/decision-making.
- Collaborate with others to meet business objectives and foster positive relationships.
Qualifications
- High School Diploma required.
- Technical Degree preferred.
- 1–2 years’ experience conducting quality inspections in a pharmaceutical setting required.
- 1–2 years’ laboratory setting experience preferred.