What are the responsibilities and job description for the Quality Assurance Associate position at Beyond a Resume?
Beyond A Resume seeks a Quality Assurance Associate for our growing biotech client in Millville, NJ.
Job Responsibilities:
- Write, revise and provide training to new and existing employees for SOPs, test specifications, protocols, and reports.
- Prepare cGMP and GDP presentations and provide training to the team.
- Inspect production procedures and logbooks to ensure they are efficient and comply with regulations.
- Assist in monthly audits.
- Record all data and results in specified forms, records, or logbooks for accuracy.
- Assist for review and ensure all completed manufacturing records are free from error before product release.
- Manage training software, enter training records, and trend all employees' trainings.
- Ensure and maintain retained samples.
Job Qualifications:
- Bachelor's degree in a related field or equivalent experience.
- Proven experience in quality assurance, preferably in a manufacturing or pharmaceutical environment.
- Strong knowledge of quality management principles, practices, and methodologies.
- Familiarity with FDA regulations, GMP, HACCP, and other relevant industry standards.
- Proficient in data collection, analysis, and reporting using statistical tools.
- Excellent attention to detail and ability to identify trends or patterns in data.
- Strong problem-solving skills and ability to implement effective solutions.
- Excellent communication skills, both written and verbal.
Job Type: Full-time
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
Schedule:
- Monday to Friday
Education:
- High school or equivalent (Required)
Experience:
- Quality assurance: 1 year (Preferred)
- GMP: 1 year (Preferred)
- Quality audits: 1 year (Preferred)
Work Location: In person
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