Document Control Specialist
Codis | St. Louis (Brentwood), Missouri
Pay: $20.00 to $30.00 per hour (based on experience)
Schedule:
- Monday through Friday
- 8:00 AM to 5:00 PM
- Full-time
- On-site
Join the Codis Team!
Codis is looking for a highly organized and detail-oriented Document Control Specialist to join our Quality Assurance team at our Brentwood, Missouri location. This position is responsible for maintaining and administering controlled quality documentation that supports FDA-regulated pharmaceutical manufacturing.
If you enjoy working in a structured environment where accuracy, organization, and attention to detail are essential, this is an excellent opportunity to build your career with a growing pharmaceutical company.
What You'll Do
As our Document Control Specialist, you'll play an important role in ensuring our documentation meets cGMP and FDA requirements by:
- Creating, revising, and maintaining Standard Operating Procedures (SOPs), Master Batch Records, forms, and other controlled documents.
- Coordinating electronic document routing, review, approval, and tracking.
- Maintaining document control files, archives, and master indexes.
- Ensuring all controlled documents comply with internal procedures and regulatory requirements.
- Managing document revisions and maintaining historical records.
- Supporting labeling revisions and controlled document updates.
- Coordinating document changes with Production, Quality, Purchasing, and Research & Development.
- Issuing logbooks, batch records, labels, and other production documentation.
- Organizing, scanning, filing, and archiving quality documents for easy retrieval.
- Coordinating required employee training notifications when new or revised documents are approved.
- Assisting with FDA, customer, and regulatory audits.
- Providing document control support to departments across the organization.
- Performing other duties as assigned.
Qualifications
We're looking for someone who has:
- High school diploma or equivalent.
- Three (3) or more years of document control or documentation experience.
- At least one (1) year of experience in a regulated industry preferred.
- Experience in pharmaceutical, biotechnology, medical device, food manufacturing, or another FDA-regulated environment is strongly preferred.
- Knowledge of current Good Manufacturing Practices (cGMP).
- Proficiency with Microsoft Office (Word, Excel, Outlook).
- Experience with Adobe Acrobat and electronic document management systems is a plus.
- Excellent organizational, proofreading, and time management skills.
- Strong written and verbal communication abilities.
- The ability to manage multiple priorities while maintaining exceptional accuracy.
Why Join Codis?
At Codis, our employees play an important role in producing high-quality pharmaceutical products that make a difference. We foster a collaborative, team-oriented environment where quality, integrity, and continuous improvement are valued every day.
We are committed to providing competitive pay, excellent benefits, and opportunities for professional growth.
Benefits
We offer a comprehensive benefits package that includes:
- Medical, Dental, and Vision Insurance
- Company-paid Life, Short-Term and Long-Term Disability Insurance
- 401(k) with Company Match โ 4% of 5%
- Paid Holidays
- 80 hours of vacation annually, beginning on your first day of employment (prorated)
- 56 hours of paid Sick/Personal Time annually
- Career growth and development opportunities
Apply Today!
If you're looking for a career with a company committed to quality, teamwork, and making an impact in the pharmaceutical industry, we'd love to hear from you.