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Quality Assurance Specialist

  • Greenville, NC, United States

$46 to $56.5 USD / hour · Contract

This opening has closed.

The original listing is kept below for reference.

Job details

Pay
$46 to $56.5 USD / hour
Job type
Contract
Closing date
Experience
Experience: Minimum 4 years of QA/QC or Operations experience in the pharmaceutical industry, with a strong preference for sterile/aseptic manufacturing processes.
Posting language
English
Posted

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Original job description

Archived listing. The details below describe a past opening.

job summary:

Join Our Client, an industry leader in pharma innovation! Seeking a Quality Specialist at Greenville , NC with a BS degree & 4+ yrs in sterile QA/pharma to drive cGMP compliance on a 2-2-3 rotation (6a-6p).

location: Greenville, North Carolina job type: Contract salary: $46.00 - 56.50 per hour work hours: 6am to 4pm education: Bachelors

responsibilities:

  • Perform daily quality assessments across classified and non-classified areas to ensure cGMP compliance and site procedure adherence.
  • Provide hands-on guidance on aseptic techniques, assist with troubleshooting equipment/process issues, and foster a strong quality culture on the production floor.
  • Conduct thorough quality reviews and approvals for batch records, procedures, forms, deviations, and change controls of moderate to high complexity.
  • Lead and participate in deviation investigations, RAPID event responses, and Root Cause Analysis as the Quality Assurance representative.
  • Identify continuous improvement opportunities and champion Practical Process Improvement initiatives across sterile manufacturing and packaging operations.

qualifications:

Education: Bachelor's degree in Technology, Engineering, Microbiology, or a related field (or an equivalent combination of education, training, and experience).

Experience: Minimum 4 years of QA/QC or Operations experience in the pharmaceutical industry, with a strong preference for sterile/aseptic manufacturing processes.

Technical & Physical Skills: Demonstrated technical writing, data analysis, and troubleshooting skills, with the physical capability for prolonged floor presence, gowning, and working a 6:00 AM - 6:00 PM 2-2-3 rotation schedule.

skills:

continuous improvement,packaging,manufacturing,process improvements,product development

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.

More about this job

Skills

  • Quality assurance
  • Regulatory compliance
  • Troubleshooting
  • Root cause analysis
  • Process improvement
  • Packaging functions
  • Pharmaceutical industry
  • Manufacturing processes
  • Technical writing
  • Data analysis
  • Packaging

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