Quality Assurance Auditor Lead
at TriPac Inc
South Bend, IN 46628, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 27 Jul, 2024 | Not Specified | 02 May, 2024 | 2 year(s) or above | Production Processes,Industrial Automation | No | No |
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Description:
QUALITY ASSURANCE AUDITOR LEAD
Tri-Pac, Inc. a contract development and manufacturing company (CDMO) specializing in liquid and aerosol filling for personal care and pharmaceutical marketers, is seeking an experienced Quality Assurance Auditor Lead for immediate addition to our fast growing team.
JOB DESCRIPTION:
The Quality Assurance Lead actively participates in quality guidance, product resolution decisions and statistical problem-solving techniques. The Quality Assurance Lead reports to the Quality Supervisor.
Education and/or Experience:
- Requires a High School degree or equivalent.
- 2-3 years relevant experience in Quality/manufacturing/ production processes
- Computer proficiency and scheduling experience required; good writing skills required.
- Familiarity with industrial automation (e.g., distributed control and PLC-based systems) Working knowledge of safety, quality systems, and GMPs is required
Responsibilities:
- Analyzing data, measuring products, and verifying all products to ensure proper quality of appearance, packaging, and decoration.
- Implement and monitor all procedures and processes as they relate to Quarantine, Hold, Expired, Damages, Return Goods and Recalled product.
- Maintains Daily Down Time Log
- Reviews daily all Manufacturing batch records required to support shift and any off-shift needs.
- Monitors QA and QC performance on the line. Fills in when QA or QC is absent.
- Provides on-the-job training for new employees in the Quality Department.
- Writing deviations and investigations as required.
- Actively involved with and mentors less experienced co-workers.
- Able to work overtime as needed.
- Other duties as assigned.
Education and/or Experience:
- Requires a High School degree or equivalent.
- 2-3 years relevant experience in Quality/manufacturing/ production processes
- Computer proficiency and scheduling experience required; good writing skills required.
- Familiarity with industrial automation (e.g., distributed control and PLC-based systems) Working knowledge of safety, quality systems, and GMPs is required.
REQUIREMENT SUMMARY
Min:2.0Max:3.0 year(s)
Pharmaceuticals
Production / Maintenance / Quality
Software Testing, Clinical Pharmacy
Diploma
Proficient
1
South Bend, IN 46628, USA