QA Inspector

Miami, FL

Posted: 09/27/2019 Job Number: JN -092019-11136
QA Inspector I

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 Inspector I
  • Location: Southwest Miami, FL
  • Industry: Pharmaceutical
  • Hours: Monday Thursday, 5am-3:30pm with OT on Friday and Saturdays
  • Salary: $16.00/hr-$18.00/hr.
  • Employment Type: Contract up to 6 months
COMPANY OVERVIEW
This environment is a specialty pharmaceutical company engaged in research, development, manufacturing of prescription pharmaceutical products.

OVERALL RESPONSIBILITIES
Perform Quality Assurance tasks such as sampling, inspections, and tests designed to ensure manufactured products are in compliance with internal SOP s, Safety initiatives, Company policies, FDA and DEA regulations. Document all work performed, ensuring accuracy and thoroughness. Inform management of any deviations from established standards/procedures.

ESSENTIAL DUTIES
  • Inspect and approve rooms, lines and equipment prior to use by manufacturing and R&D personnel.
  • Approve components for in-process operations.
  • Monitor manufacturing areas for compliance with internal SOPs, cGMPs and FDA/DEA regulations.
  • Document all work activity in appropriate batch records, forms, and logs to ensure accuracy and compliance.
  • Sample in-process items, and finished products. Perform required inspections and testing of in-process items and finished products. Process and distribute samples to different departments.
  • Review records for cGMP compliance for accuracy and thoroughness.
  • Inform management of problems, failures and deviations from established internal and regulatory standards.
  • Apply disposition sticker to components and in-process materials.
  • Issue QA Alerts whenever any questionable component, in-process material or product is identified at any stage of production or storage.
  • Perform swab and Rodac Plate sampling as required.
  • Perform transactions in JD Edwards when required.
REQUIREMENTS
  • Minimum high school diploma or equivalent
  • Minimum 3 years within a regulated/GMP environment (pharmaceutical preferred)
  • Basic computer skills required. Basic math skills required (i.e., calculating %, addition, subtraction, multiplication, division).
  • Ability to read, write, communicate and follow instructions (verbal and written) in English is required.
  • Regularly required to stand for more than one hour at a time; occasionally lifts and carries objects weighing up to 50 pounds. Visual acuity and manual dexterity required to proofread documents and operate computer.
EOE/ADA
Search words: Inspector, inspections, GMP, QA, Quality Assurance, pharmaceuticals, manufacturing, in-process materials, compliance, samples
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