QA Documentation Associate

Miami, FL

Posted: 06/01/2020 Job Number: JN -062020-11655

Job Description

QA Documentation Associate

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.
  • Title: QA Documentation Associate
  • Location: Miami, FL
  • Industry: Pharmaceutical
  • Hours: Monday Friday, 8am-5pm
  • Salary: $18.00/hr
  • Employment Type: 3-4 month contract
  • Provide administrative support to the QA Department
  • Maintain and Supervise the QA Documentation room and control of documents
  • Archive documents in line with company policies and procedures
  • Keep the Documentation room organized ensuring restricted access to GMP documents.
  • Scan, log-in and filing of executed Batch Records, Raw Materials P.O., SOPs, Temperature and Humanity Chart Recorded, Protocol, Finish and Raw Material Specifications
  • Update and replace all binders with the current effective SOPs for all Departments
  • Weekly collection and replacement of environmental temperature charts in manufacturing
  • Issue Log books for Production
  • Coordinate and ship documents for archiving off-site.
  • Able to write and follow Standard Operating Procedures (SOPs)
  • Other duties as assigned
  • Minimum 3 years experience and knowledge of Good Manufacturing Practices (GMPs) preferably pharmaceutical, nutraceutical/vitamin, food/beverage or related
  • Excellent knowledge of Windows, Word and Excel
  • Excellent clerical skills; detail oriented
  • Able to effectively communicate in English written and oral
  • Able to prioritize multiple work assignments
  • Able to see colors
  • Able to follow routine verbal and/or written instructions
  • Able to work under pressure and meet deadlines
  • Must have understanding and knowledge needed about safety SOP s and the requirements for the position to ensure a safer working environment. All precautions and processes must be adhered to in order to maintain a high level of safety compliance.
  • Minimum High School Diploma with previous experience in FDA regulated industry; Associate degree in Sciences or related discipline is a plus.
Search words: Documentation, QA, Quality Assurance, batch records, GMP, SOPs, production, manufacturing, Specialist
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