Quality Document Technician

Primary Talent Partners; Round Lake (IL); On-site; USD 30,307; Full time

Job summary

A talent acquisition firm is seeking a Quality Document Technician for a 6-month contract in Round Lake, IL. The role includes responsibilities like creating and distributing quality documentation, maintaining equipment, and identifying process improvements. Ideal candidates should have a high school diploma and experience in manufacturing or quality systems. Flexible hours are required, and candidates must not be allergic to penicillin or cephalosporin drugs. Compensation is $22.00/hr with no PTO or benefits.

Qualifications

• 6 months of experience in manufacturing/quality preferred.
• Basic science, math, and digital literacy (Microsoft Word and Excel) are required.
• Strong writing and verbal communication abilities needed.
• Attention to detail and organization are highly desired.

Responsibilities

• Make detailed observations, analyze data, and interpret results.
• Create, verify, and distribute quality documentation for manufacturing.
• Support Document Center Technicians with standard office work.
• Maintain department equipment and inventory levels.
• Identify process improvements and escalate to management.

Skills

Basic science skills

Math skills

Microsoft Word proficiency

Microsoft Excel proficiency

Good writing skills

Verbal communication skills

Problem-solving skills

Attention to detail

Organizational skills

Education

High School Diploma or equivalent

Job description

1 day ago Be among the first 25 applicants

Primary Talent Partners has a new contract opening for a Quality Document Technician with our healthcare client in Round Lake, IL. This is a 6‑month contract with a potential for extension.

Pay: $22.00/hr; W2 contract, no PTO, no Benefits. ACA‑compliant supplemental package available for enrollment.

Description

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 ***

Qualifications

• 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.

Equal Opportunity / Affidavits

Primary Talent Partners is an Equal Opportunity / Affidavit employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, national origin, disability, protected veteran status, gender identity, or any other factor protected by applicable federal, state, or local laws.

If you are a person with a disability needing assistance with the application or at any point in the hiring process, please contact us at [e-mail].

Seniority level

• Entry level

Employment type

• Contract

Job function

• Quality Assurance

Industries

• Medical Equipment Manufacturing