Quality Assurance Specialist I

LifeScience Logistics•Union City, GA

11d•Hybrid

About The Position

The Quality Assurance Specialist I will provide support during regulatory inspections and audits, manage quality system documentation, and ensure regulatory compliance. This role involves planning and presenting Quality System information, initiating and approving change controls, deviations, and recalls. The specialist will also be part of the internal audit team, assist in external audits, and review product-specific paperwork. Additionally, they will collaborate with operations and facilities teams to determine root causes of discrepancies, develop corrective actions, revise SOPs, and perform Gemba walks applying Six Sigma concepts. The position requires participation in cross-functional initiatives within a 3PL environment, assisting with validation projects, and managing temperature monitoring systems. The role also includes performing record reviews, assisting in returns and damages processes, and participating in an after-hours ISM rotation program.

Requirements

Minimum of 1-3 years’ experience in a quality, preferably a logistics role.
Strong understanding of a 3PL business, audits and complaints procedures is preferred.
Validation and DEA experience strongly preferred.
Medical Device, Pharma, and Plasma experience preferred.
Experience in temperature monitoring of controlled environments.
Effective time management skills.
Impeccable verbal and written communication skills.
Ability to conduct appropriate research as needed.
Strong presentation skills.
Attention to detail and organization.
Critical thinking.
Take ownership.
High standard.
Training – public speaking.
Ability to take Constructive Criticism.
Interest in working in a fast-paced environment.
Deftly navigate through Quality and Warehouse Management Systems with training – COMPLIANCE QUEST, Tecsys Elite, WebCTRL.
Intermediate Microsoft Office skills: Outlook, Excel, PowerPoint.
Certified auditor training per ASQ or ISO (preferred).
Demonstrated skills and practice of Six Sigma/statistics and process capability/FMEA is preferred.
Conversant with cGMPs, Quality Systems and CAPAs per 21 CFR 210/211 and 820.
Verifiable aptitude of FDA, OSHA, and DEA regulations.
Intermediate public speaking and presentation skills.
Excellent verbal and written communication skills.
Must be able to successfully pass all preliminary employment requirements (i.e., background check and drug screen).
Must be able to travel up to 10%.
Must have a valid driver’s license.
Work is light to medium in nature with frequent walking to perform assigned tasks.
Must be able to safely conduct occasional lifting of 25 - 50 lbs.
Ability to handle multiple priorities and solve inquiries and issues expeditiously and efficiently.
Must be able to read at a distance, close to the eyes, and at arm’s length with or without correction.

Nice To Haves

Bachelor of Science (BS) degree in Engineering, Science, Logistics, or related field preferred.
Strong understanding of a 3PL business, audits and complaints procedures is preferred.
Validation and DEA experience strongly preferred.
Medical Device, Pharma, and Plasma experience preferred.
Certified auditor training per ASQ or ISO (preferred).
Demonstrated skills and practice of Six Sigma/statistics and process capability/FMEA is preferred.

Responsibilities

Provide support during regulatory FDA, DEA, State inspections and customer audits.
Plan and present Quality System information to internal and external groups.
Initiate, review, and approve Change Controls, Recalls, Deviation for nonconformances, & Reactive Maintenance.
Work to maintain Quality Systems policies and procedures to ensure regulatory compliance.
Be a part of the internal audit team and assist in external audits.
Release “quarantined” product upon receipt of documentation from Client and use Hold and Release process, take part in Recall.
Review/approve product-specific paperwork particular to Client guidelines, Deviations and CAPAs.
Assist in Operations and Facilities team in determining root cause of discrepancies and help develop corrective actions and verification activities.
Revise SOPs and WIs for process enhancement.
Perform Gemba walk applies six sigma concepts such as 5S’s.
Participate in cross-functional initiatives for a 3PL environment.
Assist in returns and damages process.
Perform record reviews to ensure compliance with all applicable procedures and regulations.
Take part on ISM (Inventory System Management) after hours rotation program.
Assist in validation projects.
Being able to be on call for WebCTRL temperature monitoring on a rotation program.
Assist in generating and reviewing temperature monthly reports in a timely manner.
Other duties as assigned.