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Document Control Manager Jobs in Springfield, MO

AMRI

Manager, Quality Control

Springfield, MO

Manager, Quality Control in Springfield, MO Build your future at Curia, where our work has the ... Ensure staff have appropriate documented training prior to assigning work. Compliance ...

Creative Modular Construction

Be Seen First

Document Controller & QA Administrator

Springfield, MO · On-site

$62K - $80K/yr

... document control, records management, and QA administration experience required • 5+ years in construction, manufacturing, or ISO 9001 environments preferred • Experience working with senior ...

HiFyve

Mechanical Design Engineer II

Springfield, MO

$71K - $100K/yr

Maintain document control procedures and apply lessons learned to future projects * Support design ... Ability to manage multiple projects in a time-sensitive environment * Strong written and verbal ...

Astrix Inc

QC Deviation Specialist III

Springfield, MO · On-site

$45 - $47/hr

Perform and document Deviation Investigations for Manufacturing and Quality Control operations ... Support continuous improvement initiatives within the Quality Management System (QMS). * Ensure all ...

AMRI

Quality Control Analyst I, II or III

Springfield, MO · On-site

$20.25 - $27.25/hr

Enter data into relevant data management systems. Perform tracking and trending of data as ... Strict compliance with all cGMP documents SOP's, Batch records, protocols, change controls ...

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All JobsDocument Control JobsDocument Control Manager JobsDocument Control Manager Jobs in Springfield, MO

Document Control Manager information

See Springfield, MO salary details

$32.9K

$93.1K

$148.7K

How much do document control manager jobs pay per year?

As of Jun 9, 2026, the average yearly pay for document control manager in Springfield, MO is $93,104.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,600.00 and $111,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Document Control Manager, and why are they important?

To thrive as a Document Control Manager, you need deep knowledge of document management processes, attention to detail, and often a degree in business administration or a related field. Familiarity with document management systems (DMS) such as SharePoint, Aconex, or similar platforms, along with certifications like ISO 9001, is typically required. Strong organizational skills, effective communication, and the ability to lead teams set top performers apart. These competencies ensure accurate, secure, and efficient handling of critical documents, supporting compliance and smooth project workflows.

What Is a Document Control Manager?

A document control manager oversees document management systems in an organization, often in design, construction, or engineering fields. As a control manager, you track, file, update, and destroy documents as appropriate. You use a database or filing system to manage confidential business and client documents. Your responsibilities include running software for document maintenance, following procedure requirements for confidentiality and accuracy, and improving processes. Your duties may involve supervising a team of employees, establishing databases, assigning projects, and ensuring compliance and quality control. Qualifications include experience in document management systems, industry knowledge and skills, and for some jobs, a college degree.

What are Document Control Managers?

Document Control Managers are professionals responsible for overseeing the management, organization, and security of documents within an organization. They ensure that all company documents are properly stored, easily accessible, and compliant with regulatory requirements. Their duties often include implementing document control procedures, managing document workflows, and training staff on document management systems. Document Control Managers play a crucial role in maintaining data integrity and supporting efficient operations.

What are some common challenges a Document Control Manager may face when implementing new document management systems within an organization?

Document Control Managers often encounter challenges such as resistance to change from staff, integrating new systems with existing workflows, and ensuring data security and compliance with industry regulations. Successfully overcoming these hurdles typically involves providing thorough training, clear communication about the benefits of the new system, and collaborating closely with IT and other departments. Additionally, establishing standardized processes and regular audits can help maintain consistency and quality in document management practices.

What is the difference between Document Control Manager vs Document Coordinator?

AspectDocument Control ManagerDocument Coordinator
ResponsibilitiesOversees document management systems, ensures compliance, manages teams, and implements proceduresAssists with document preparation, updates, and distribution under supervision
CredentialsTypically requires a degree in engineering, management, or related field; certifications like ISO or document control certifications are commonOften requires a high school diploma or associate degree; certifications are less common
Work EnvironmentIndustrial, construction, engineering, or manufacturing settingsOffice-based, supporting project teams in various industries

The Document Control Manager holds a leadership role with strategic responsibilities, while the Document Coordinator provides operational support. Both roles are essential for effective document management but differ in scope and seniority.

What is a document control manager?

A document control manager oversees the management, organization, and distribution of company documents to ensure accuracy, compliance, and accessibility. They often use document management systems and require strong organizational and communication skills to maintain version control and audit trails.
More about Document Control Manager jobs
What are the most commonly searched types of Document Control jobs in Springfield, MO? The most popular types of Document Control jobs in Springfield, MO are:
What job categories do people searching Document Control Manager jobs in Springfield, MO look for? The top searched job categories for Document Control Manager jobs in Springfield, MO are:
What cities near Springfield, MO are hiring for Document Control Manager jobs? Cities near Springfield, MO with the most Document Control Manager job openings:
Document Control Manager jobs near you
Infographic showing various Document Control Manager job openings in Springfield, MO as of June 2026, with employment types broken down into 2% As Needed, 86% Full Time, 8% Part Time, and 4% Contract. Highlights an 100% In-person job distribution, with an average salary of $93,104 per year, or $44.8 per hour.
Manager, Quality Control

Manager, Quality Control

Curia, Inc.

Springfield, MO • On-site

Full-time

Retirement

Posted 23 days ago

Curia rating

7.6

Company rating: 7.6 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

Job description

Job Description
Manager, Quality Control in Springfield, MO
Build your future at Curia, where our work has the power to save lives
Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives.
We proudly offer
  • Generous benefit options (eligible first day of employment)
  • Paid training, vacation and holidays (vacation accrual begins on first day of employment)
  • Career advancement opportunities
  • Education reimbursement
  • 401K program with matching contributions
  • Learning platform
  • And more!

Summary:
If you believe that the details matter and take satisfaction in work done right, this role is for you. At Curia, we operate from a simple truth: lives depend on the work we do. As the Quality Control Manager, you'll lead a team that takes that responsibility seriously, ensuring the integrity of our testing, documentation, and compliance practices every day.
In this role, you'll oversee the full scope of QC operations at the site, driving compliance with applicable regulatory requirements through rigorous testing, trend analysis, continuous improvement, and results reporting. You'll mentor and develop your team, manage complex investigations, and serve as a key quality leader who embodies the Curia Way through accountability, curiosity, and a commitment to excellence.
Essential Responsibilities
QC Operations & Testing
  • Manage and prioritize testing operations for samples and incoming, in-process, and final products.
  • Oversee and perform pharmaceutical analysis to support manufacturing and site operations.
  • Ensure QC functions are completed in accordance with company and governmental standards of safety and quality, with complete and timely experimental documentation.
  • Organize workload and coordinate activities to carry out multiple projects concurrently in alignment with established objectives, timelines, and deadlines.

Team Leadership & Development
  • Lead, motivate, and develop a team of analysts and technicians, supporting their education, performance, efficiency, and productivity.
  • Mentor and train team members on applicable techniques, equipment, and procedures.
  • Ensure staff have appropriate documented training prior to assigning work.

Compliance & Investigations
  • Maintain compliance with regulations at all levels and ensure strict adherence to SOPs and cGMPs.
  • Manage all OOS investigations, deviations, change control activities, and CAPAs within the QC function.
  • Ensure laboratory operations are conducted safely; remain familiar with the Chemical Hygiene Plan and enforce full compliance with safety rules.
  • Escalate quality concerns to the Quality department, along with proposed solutions.

Additional Duties
  • Support broader quality and business needs as reasonably assigned.

Good Manufacturing & Documentation Practices
Quality is something we take pride in together. You'll perform your work in alignment with cGMP requirements and Curia's standards, which means:
  • Perform all documentation in compliance with ALCOA++ principles and site SOPs.
  • Adhere to applicable cGMP documents including SOPs, batch records, protocols, change controls, and controlled forms.
  • Keep all required cGMP training current and escalate quality concerns along with proposed solutions to the Quality department.

Education & Experience
Required
  • Bachelor's degree (BA/BS) in a relevant field with a minimum of 5 years of relevant work experience, including 2 years in a team leadership role.
  • OR a Master's degree (MA/MS) in a relevant field with a minimum of 3 years of relevant work experience, including 2 years in a team leadership role.

Preferred
  • Advanced degree in Chemistry, Analytical Chemistry, or a related field.
  • Prior experience with FDA GMPs (21 CFR 211, 820, and/or 600), ISO 9001, and ISO 13485.

Knowledge, Skills & Abilities
  • Expert-level knowledge of cGMP, USP, EP, and FDA regulations.
  • Technical competence including the understanding of theory and interpretation of a full range of laboratory techniques.
  • Proficiency in HPLC and GC method development and method validation, with extensive experience across multiple analytical techniques and equipment.
  • Strong oral and written communication skills, including effective listening and the ability to engage cross-functional teams.
  • Demonstrated ability to recognize what needs to be done, take initiative, and drive results.
  • Proven ability to effectively utilize team resources and manage competing priorities.
  • Proficient use of Microsoft Office Suite (Excel, Word) and other required software.
  • Strong organizational skills with the ability to multi-task and meet deadlines.

Physical requirements
This role regularly requires sitting, standing, and using hands to handle or feel materials. The employee will frequently use hands and arms and communicate verbally and in writing. Occasional walking, climbing, balancing, stooping, kneeling, and crouching may be required. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities include close vision and the ability to adjust focus.
Work environment
This position operates in a regulated manufacturing environment. The employee may be occasionally exposed to fumes, airborne particles, toxic or caustic chemicals (Personal Protective Equipment required), wet or humid conditions, moving mechanical parts, high or precarious places, and moderate noise levels. Risk of electrical shock may be present.
The employee will be responsible for generating hazardous waste for treatment, storage, and disposal, and must be familiar with applicable training requirements under the Resource Conservation and Recovery Act, including waste labeling, secondary containment, chemical compatibility, storage time limits, container integrity, and proper disposal protocols.
This job description reflects the general nature and scope of the role and is not exhaustive. We're a growing organization, and opportunities to contribute beyond this list are part of what makes Curia exciting. We're committed to reviewing reasonable accommodation requests to enable individuals with disabilities to perform the essential functions of this role
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.
All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.

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