2nd or 3rd Shift Quality Assurance Specialist - Liquid Media

Job Description

Job Description

A-Line Staffing is now hiring a 2 nd or 3 rd Shift Liquid Media Quality Assurance Specialist in Mebane, NC. The Liquid Media Quality Assurance Specialist would be working for a major healthcare organization and has career growth potential. This would be full time / 40 hours per week.

If you are interested in this Liquid Media Quality Assurance Specialist position, please apply to this posting for Immediate Consideration!

Liquid Media Quality Assurance Specialist Compensation

• The pay rate for this position is $27.10 per hour for 2nd Shift and $27.50 per hour for 3rd shift
• Benefits are available to full-time employees after 90 days of employment and include PTO, paid holidays, health, optical, dental, life, and short-term disability insurance
• A 401(k) with a company match is available for full-time employees with 1 year of service on our eligibility dates

Liquid Media Quality Assurance Specialist Highlights

• 100% Onsite in a state-of-the-art medical manufacturing facility in Mebane, NC

Schedule Options:

·         2nd shift: 3pm-11:30pm Monday - Friday

·         3rd Shift: 3rd Shift 11pm-730am, Sunday - Thursday

Position Summary:

The QA Specialist - Liquid Media is an on-the-production-floor quality role responsible for supporting manufacturing operations through real-time compliance oversight and in-process quality assurance activities. This position ensures adherence to Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) throughout production.

The role focuses on execution of quality activities including line clearance verification, in-process inspection, documentation review, and identification of nonconforming conditions. The QA Specialist collaborates closely with Manufacturing, Quality Control, Engineering, and Maintenance to ensure product quality and compliance. This position supports investigations through data collection and documentation review but does not own advanced root cause analysis or engineering-level problem solving.

Liquid Media Quality Assurance Specialist Responsibilities

·         Provide daily, hands-on quality support on Liquid Media production lines.

·         Assist as needed to verify line setup and line clearance activities.

·         Perform in-process quality checks and spot inspections to ensure adherence to procedures and specifications.

·         Conduct real-time review of production documentation for accuracy, completeness, and legibility.

·         Ensure compliance with GDP requirements and identify documentation errors for correction.

·         Monitor and escalate recurring documentation issues to supervision for corrective action.

·         Detect and document nonconforming conditions during production and inspection activities, and initiate containment actions.

·         Perform preliminary fact gathering to support investigations.

·         Escalate complex issues to Quality Engineers or appropriate technical functions.

·         Support investigations through documentation review and data collection.

·         Partner with Manufacturing, Engineering, Maintenance, and Product Support to resolve quality-related issues.

·         Provide guidance to production associates on quality requirements and documentation expectations.

·         Coordinate or assist with sample preparation and submission to the QC laboratory.

·         Serve as the on-floor quality representative to ensure compliance with procedures and regulatory requirements.

·         Promote awareness of quality standards, defect prevention, and GDP compliance.

·         Escalate risks and quality concerns in a timely manner.

Liquid Media Quality Assurance Specialist Required Qualifications

·         Minimum of 2 years of experience in manufacturing or quality within an FDA-regulated or ISO 13485 environment.

·         Bachelor's degree, or 4 additional years of experience in manufacturing or quality.

·         Basic knowledge of Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP).

·         Experience with inspection, documentation review, or production support activities.

·         Strong attention to detail with the ability to identify errors and nonconformances.

·         Ability to work independently and collaboratively in a fast-paced production environment.

·         Effective communication skills with experience interacting with production and cross-functional teams.

·         Proficient in Microsoft Office and other basic computer applications.

Preferred Qualifications

·         Familiarity with sampling plans and inspection standards.

·         Experience supporting production floor quality activities.

·         Basic understanding of nonconformance processes.

Necessary Skillset

·         Ability to assess the immediate quality impact of events observed on the production floor and support appropriate escalation, containment, and documentation in accordance with established procedures and quality system requirements.

·         Sound independent judgment in identifying potential compliance or product quality concerns, prioritizing issues, and taking appropriate action within defined responsibilities while recognizing when escalation is needed.

·         Strong working knowledge of Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) in a regulated manufacturing environment.

·         Strong attention to detail with the ability to identify documentation errors, process deviations, and nonconforming conditions in real time.

·         Effective communication and collaboration skills for working with Manufacturing, Quality Control, Engineering, Maintenance, and other cross-functional teams.

·         Ability to perform documentation review and basic fact gathering to support investigations and issue resolution.

·         Ability to work effectively in a fast-paced production environment while maintaining a high standard of compliance, accuracy, and responsiveness.

If you think this Liquid Media Quality Assurance Specialist position is a good fit for you, please feel free to apply to this posting!