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Quality Assurance Technician/Auditor (Pharmaceuticals)
cybotic systems Decatur, IL
$84k-101k (estimate)
Full Time 2 Weeks Ago
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cybotic systems is Hiring a Quality Assurance Technician/Auditor (Pharmaceuticals) Near Decatur, IL

Role: QA Technician/Auditor

Location: Decatur, Illinois

Duration: Full Time

Experience: 01 - 10 Year

Position Summary:

  • The QA Technician performs quality assurance duties to prevent or eliminate defects in products for sterile filling operations or in final inspection and packaging operations.
  • This individual must work in a detail-oriented, compliant manner in a high-stress environment where adherence to deadlines is critical.
  • The individual must display an exemplary level of integrity at all times.
  • Manage a workload of varying priorities while adhering to strict deadlines.

Essential Duties & Responsibilities:

  • Monitor the production process and ensure consistency of procedures.
  • Perform visual inspection of finished product.
  • Perform AQL testing of finished product.
  • Review in process documentation.
  • Audit manufacturing rooms for adherence to cGMP and SOPs Audit the maintenance of a clean and sanitary environment.
  • Review daily/weekly/monthly and bi-monthly logbook entries for completeness.
  • Review, approve and issue verified -clean green release stickers to operations.
  • Check machine settings.
  • Observe/mentor personnel on aseptic performance.
  • Perform line clearances and review documentation (circular charts, autoclave tapes etc.) to allow operations to initiate production (release to fill).
  • Obtain and maintain gown certification for clean room entry.

Education and Experience:

  • Associate's Degree or equivalent from a two-year college or technical school;
  • One year related experience and/or training; or equivalent combination of education and experience.

Job Prerequisites:

  • All full-time employees are required to work a 40-hour week.
  • At times, additional hours during the weekdays, evenings, and/or weekends will be required to complete tasks and meet deadlines.
  • All applicants must be able to meet the attendance standards.
  • Must have a complete knowledge of current Good Manufacturing Practices, United States Pharmacopeia, current Code of Federal Regulations (21 CFR parts 11, 210, 211, 820), and other FDA regulations and guidances.
  • Have general math skills: adding, subtracting, multiplication, division, and percentage calculation.
  • Ability to calculate figures and amounts such as discounts, interest, commissions, and proportions.
  • Able to use personal computer and standard office equipment such as fax and copy machines, calculators, and printers.
  • Aptitude to learn computer programs as needed (i.e. Microsoft Office Word, Excel) in addition to other business applications.
  • Strong verbal and written communication skills.
  • Resourceful and well organized.
  • Ability to read and interpret standard documents such as: procedure manuals, employee handbook, and job related publications.
  • Ability to write routine reports and correspondence.
  • Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.
  • Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.

Job Type: Full-time

Pay: $31.00 - $34.00 per hour

Benefits:

  • 401(k)
  • Dental insurance
  • Health insurance
  • Life insurance
  • Paid time off
  • Vision insurance

Experience level:

  • 3 years
  • 4 years
  • 5 years

Schedule:

  • Day shift
  • Monday to Friday

Work setting:

  • In-person

Experience:

  • QA(Pharma): 5 years (Required)
  • liquid sterile injectables and liquid dosages: 2 years (Required)

Work Location: In person

Job Summary

JOB TYPE

Full Time

SALARY

$84k-101k (estimate)

POST DATE

05/12/2024

EXPIRATION DATE

05/15/2024

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