Quality Assurance Specialist II

Reposted 22 Days Ago
Be an Early Applicant
Apex, NC, USA
In-Office
Junior
Healthtech • Logistics
The Role
The Quality Assurance Specialist II reviews compliance records, assists with audits, maintains quality files, and supports process improvement within logistics.
Summary Generated by Built In

RESPONSIBILITIES:

  • Reviews and approves Change Requests, Reactive Maintenance, Deviations/CAPA as assigned
  • Assist with validations as assigned
  • Review records and forms to ensure compliance with established LSL procedures and regulations
  • Maintain Quality files as applicable: Scan, Save to appropriate online storage, file
  • Perform warehouse walkthroughs to ensure the facility is maintained in a clean, safe, compliant manner
  • Be a part of the internal audit team and assist in external audits
  • Assist with the DEA program
  • Assist QA Supervisor and CQCU in developing plans and programs for process improvement
  • Interact with state and federal agencies, clients, and corporate quality group
  • Plan and present Quality System information to internal and external groups
  • Work with Quality Systems and all levels of facility personnel to achieve company quality standards
  • Perform Holds and Releases as directed by clients which can include temptale downloads as needed
  • Assist in the Returns, Damage and Recall processes
  • Review and approve inventory adjustments
  • Notify QA Supervisor and CQCU of any unusual trends
  • Perform training on Quality related documents when necessary
  • Other duties as assigned

QUALIFICATIONS AND JOB SPECIFICATIONS:

  • Bachelor of Science (BS) degree in Engineering, Science, or related field preferred
  • Minimum of 1-3 years’ experience in a quality role, preferably in a logistics setting  
  • Conversant with cGMPs, Quality Systems, and CAPAs
  • Strong understanding of a 3PL business, audits and complaints procedures
  • Medical Device, Pharma and DEA experienced preferred
  • Knowledge of electronic document systems

  • Demonstration of the following:
  • 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, and
  • Interest in working in a fast-paced environment

TECHNICAL EXPERTISE:

  • Deftly navigate through Quality and Warehouse Management Systems with training – MQ1, 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
  • 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

 

ADDITIONAL EMPLOYMENT REQUIREMENTS

  • Must be able to successfully pass all preliminary employment requirements (ie. background check and drug screen)
  • Must have a valid driver’s license

PHYSICAL/MENTAL/VISUAL DEMANDS

  • 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

 

WORKING CONDITIONS

  • Activities occur within a typical office environment
  • 25% of time will be spent in a warehouse setting
  • 15 % of time will be spent on key entry

 

EQUIPMENT OPERATED

  • Equipment:  Laptop computer, cell phone, fax machine, copier, and desk phone
  • Systems: Outlook, Excel, Word, PowerPoint, WebCTRL (Temperature Monitoring Software), TECSYS (WMS – Warehouse Management System), and MQ1 (Quality Management Software)
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

Top Skills

Dea Regulations
Fda
MS Office
Mq1
Osha
Tecsys Elite
Webctrl
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The Company
HQ: Coppell, TX
214 Employees
Year Founded: 2006

What We Do

LifeScience Logistics, founded in 2006, is a third party logistics company committed to offering the highest quality, flexibility, and compliance in Healthcare Supply Chain Solutions. LSL operates out of four cGMP compliant and FDA registered facilities (Atlanta, GA, Baltimore, MD, Indianapolis, IN and DFW Airport, TX) totaling more than 1.35 million SF of fully validated and temperature mapped space. Our facilities allow for Control Room Temperature (CRT) and Cold Chain Capabilities; both refrigerated (2 to 8 C) and frozen (-20 C) storage. LSL is a Board of Pharmacy licensed distributor, VAWD-accredited, cGMP and FDA compliant company. Our can-do attitude, and efficient operations, set us apart from our competition. We pride ourselves on our ability to bring the best technology, quality, and intellectual capital to our clients. LifeScience Logistics can be found on the web at www.lslog.com. To get LifeScience Logistics news direct, visit http://www.lslog.com/News/Recent.aspx.

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