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Document Control Specialist
Document Control SpecialistIntegrated Resources, Inc ( IRI ) • Round Lake, IL, US
Document Control Specialist

Document Control Specialist

Integrated Resources, Inc ( IRI ) • Round Lake, IL, US
[job_card.variable_hours_ago]
[job_preview.job_type]
  • [job_card.full_time]
[job_card.job_description]

Summary :

The Quality Document Technician is responsible for various assignments supporting

  • quality systems and ensuring that required documents are created and organized for use in manufacturing and for releasing products.

What you'll be doing :

  • Makes detailed observations, analyzes data, and interprets results.
  • Create, verify, and distribute quality documentation required for manufacturing.
  • Support Document Center Technicians with standard office work and for batch release.
  • Maintains department equipment and inventory levels for controlled materials.
  • Identifies process improvements and escalates to Quality Supervision and / or Management.
  • Ability to work independently and as part of a team in a fast-paced environment.

    • What you'll bring :

  • Basic science, math, and computer skills (including Microsoft Word and Excel) are required.
  • Good writing, verbal communication, and problem-solving skills are required.
  • Ability to work in a team environment and make independent decisions based on procedural and regulatory requirements.
  • It is desirable for the candidate to have experience with the requirements of current Good Manufacturing & Documentation Practices in pharma manufacturing facilities.
  • The candidate must be able to work flexible hours in a dynamic environment with minimal direct supervision.
  • The ability to work on some weekends is required.
  • Will work in both Drug Delivery and Penicillin facilities as needed.
  • Overtime may be required to meet the production schedule.
  • The candidate must not be allergic to penicillin or cephalosporin drugs
  • The candidate must not be allergic to penicillin or cephalosporin drugs
  • 6 months of experience in manufacturing / quality preferred
  • HS Diploma or equivalent is required
  • Basic science, math, and digital literacy (including Microsoft Word and Excel) are required.
  • Strong writing and verbal communication abilities, as well as problem solving capabilities are needed.
  • Attention to detail and organization are highly desired
  • It is desirable for the candidate to have experience with the requirements of current Good Manufacturing & Documentation Practices in medical devices / pharma manufacturing facilities.
  • Be able to work flexible hours in a dynamic environment with minimal direct supervision. Ability to work some Saturdays is required.
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    Document Control Specialist • Round Lake, IL, US

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