Quality Assurance Specialist job in Freeport, TX
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Freeport, TX CorTech LLC
| Job Ref: | 365910 |
| Employer: |
CorTech LLC |
| Job Type: | Contract |
| Salary and Benefits: | 20.00/Per Hour |
| Remote: | No |
Location |
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| City: | Freeport, TX |
| Post Code: | 77541 |
| Map: |
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Description |
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JobsRUs.com. is seeking to hire a Quality Assurance Specialist for our client in Freeport, TX! Pay rate: $20.00/hr. Duration: 6 months, not contract to hire at this time Location: Freeport TX - Onsite Shift: M-F 8-5pm Top 3 Skills/Requirements: Excellent attention to detail and analytical skills. Good communication and interpersonal skills. Good administrative skills Title of Position: Quality Assurance Coordinator Interview Process: Initial phone screen Onsite/in person interview Education: High School Diploma Required Skills: Good administrative skills Good communication and interpersonal skills Excellent attention to detail and analytical skills. The Quality Assurance Coordinator is involved in batch record review, ensures manufacturing records are complete, accurate, and compliant, and identifies any non-conformances and participates in CAPA (Corrective and Preventive Action) activities including deviation investigations. Key Responsibilities: Batch Record Review: ? Reviews executed batch records, master batch records, and other relevant documentation. ? Ensures records are complete, accurate, and compliant with Good Manufacturing Practices (GMP) and regulatory requirements. ? Identifies potential deviations or non-conformances during the review process. Quality Assurance Support: ? Provides ongoing quality assurance support for manufacturing processes and critical utilities. ? Participates in the development and implementation of quality assurance programs and procedures. ? Conducts assessments, gathering information through interviews, flow charting, and other techniques. Documentation: ? Reviewing and approving QA-driven documentation, such as Standard Operating Procedures (SOPs) and work instructions. ? Maintaining and updating records and documentation. Other Duties: ? Overseeing review and audit of various reports. ? Writing, reviewing, analyzing, and revising SOPs. Skills and Qualifications: ? Strong understanding of GMP and regulatory requirements. ? Excellent attention to detail and analytical skills. ? Ability to identify and resolve quality issues. ? Good communication and interpersonal skills. ? Knowledge of relevant manufacturing processes and technologies. ? Experience with batch record review and quality assurance activities. | |
ref: (365910)
86 days ago
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