What are the responsibilities and job description for the Document Control Specialist I position at Planet Pharma?
Document Control Specialist I
Round Lake, IL
6 Month Initial Contract
Pay: $21/hr
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.
• *** 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.
Salary : $21