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Document Control Specialist Medical Device Jobs in Decatur, AL

Responsibilities Peraton is seeking an experienced systems Asset Control Specialist to join our ... Completely uninstall, account for and secure each decommissioned device. * Monitor the state of all ...

Responsibilities Peraton is seeking an experienced systems Asset Control Specialist to join our ... Completely uninstall, account for and secure each decommissioned device. * Monitor the state of all ...

Responsibilities Peraton is seeking an experienced systems Asset Control Specialist to join our ... Completely uninstall, account for and secure each decommissioned device. * Monitor the state of all ...

... documentation whether manual or electronically. • Keep work area clean and organized. • Place scrap components in appropriate red scrap bins. • Notify supervisor/manager pf any recurring ...

Supervise document control personnel and compliance auditor specialists as assigned. * Promote a culture of accountability, quality, and regulatory adherence. Basic Qualifications. * Bachelor ...

Supervise document control personnel and compliance auditor specialists as assigned. * Promote a ... medical condition, genetic information, pregnancy, family structure, marital status, ancestry ...

Supervise document control personnel and compliance auditor specialists as assigned. * Promote a culture of accountability, quality, and regulatory adherence. Basic Qualifications. * Bachelor ...

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Document Control Specialist Medical Device information

See Decatur, AL salary details

$13

$26

$49

How much do document control specialist medical device jobs pay per hour?

As of Jun 22, 2026, the average hourly pay for document control specialist medical device in Decatur, AL is $26.10, according to ZipRecruiter salary data. Most workers in this role earn between $18.94 and $29.95 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Document Control Specialist in the medical device industry, and why are they important?

To thrive as a Document Control Specialist in the medical device industry, you need strong attention to detail, organizational skills, and familiarity with regulatory requirements, usually supported by a relevant degree or experience in quality systems. Proficiency with document management systems (DMS), electronic quality management systems (eQMS), and knowledge of standards such as ISO 13485 and FDA 21 CFR Part 820 is essential. Excellent communication, problem-solving, and time management skills help ensure accurate documentation and effective collaboration across teams. These skills and qualifications are crucial for maintaining compliance, ensuring product quality, and supporting successful audits in a highly regulated environment.

What is the difference between Document Control Specialist Medical Device vs Quality Assurance Specialist Medical Device?

AspectDocument Control Specialist Medical DeviceQuality Assurance Specialist Medical Device
Primary FocusManaging and maintaining controlled documentation and recordsEnsuring product quality and compliance through audits and process improvements
CertificationsISO 13485, FDA regulations familiarityISO 13485, Six Sigma, or quality management certifications
Work EnvironmentDocument management systems, compliance departmentsQuality labs, manufacturing, or compliance teams
Employer UsageMedical device companies, regulatory agenciesMedical device manufacturers, quality departments

The main difference is that Document Control Specialists focus on managing documentation to ensure regulatory compliance, while Quality Assurance Specialists focus on overall product quality and process improvements. Both roles are essential in the medical device industry and often collaborate to meet industry standards.

What are Document Control Specialists in the medical device industry?

Document Control Specialists in the medical device industry are professionals responsible for managing and maintaining all documentation related to product development, manufacturing, and compliance. They ensure that documents, such as standard operating procedures, work instructions, and quality records, are accurately maintained, properly archived, and easily retrievable. These specialists play a crucial role in ensuring that all documentation meets regulatory standards, such as FDA and ISO requirements, which is essential for product safety and market approval. Their work helps companies maintain compliance, streamline audits, and support quality assurance processes.

What are some common challenges faced by a Document Control Specialist in the medical device industry?

One common challenge for Document Control Specialists in the medical device sector is ensuring strict compliance with regulatory standards such as FDA 21 CFR Part 820 and ISO 13485. This often involves managing multiple document versions, coordinating timely reviews and approvals, and maintaining audit-ready records. Specialists must work closely with quality assurance, engineering, and regulatory teams to resolve discrepancies and implement updates efficiently. Effective communication and attention to detail are essential to prevent errors that could impact product quality or regulatory compliance.
What are popular job titles related to Document Control Specialist Medical Device jobs in Decatur, AL? For Document Control Specialist Medical Device jobs in Decatur, AL, the most frequently searched job titles are:
What cities near Decatur, AL are hiring for Document Control Specialist Medical Device jobs? Cities near Decatur, AL with the most Document Control Specialist Medical Device job openings:
Document Control Specialist - ERC

Document Control Specialist - ERC

ERC, Inc.

Redstone Arsenal, AL • On-site

Full-time

Medical, Retirement, PTO

Posted 17 days ago


Job description

Job Title
Document Control Specialist - ERC
Career Level
Experienced (Non-Manager)
Job Type
Full-Time
Location
RWESS - Redstone Arsenal - Huntsville, AL 35808 US (Primary)
Job Description
For more than 30 years, ERC has been delivering the advantage needed to solve our customers' and the nation's toughest challenges. ERC is a trusted partner to the Defense and Space communities. We provide the advanced engineering, innovative technology, and subject-matter expertise to deliver the mission results our customers need to keep the nation safe and secure. Our unique solutions enhance readiness, optimize performance, and help ensure success in the air, on the ground and in space.
An essential part of our success is our corporate culture built on respect, empowerment, and collaboration. Our culture elevates our people, ensuring they provide best-in-class service and solutions to our customers. We always strive to do the right thing. We believe that are our people are our best asset and human connection our greatest strength.
Check us out on ERC.US
Your role:
As the Document Control Specialist , your role will be to manage and ensure that the performance, function, and appearance of our products are consistent with military standards. This involves managing the functional requirements, design, and operational information throughout each product's lifecycle. You will also develop migration plans and help oversee design deployment.
What you'll do all day:
  • The Document Control Specialist will be responsible for configuration management planning product configuration identification, configuration change management, configuration status, configuration verification and audit support to product teams in development of instrumentation for missile, aviation, and sensor systems.
  • The DCS Specialist will properly document traceability of designs to requirements.
  • The DCS identifies and documents system elements, interfaces, and interdependencies.
  • Controls and documents approved changes (Engineering Change Proposals- ECPs) to product baselines in a thorough and timely manner in changes in all affected items and documentation.
  • Maintains a complete audit trail of design decisions and modifications throughout product or system life-cycle.
  • Develops DCS policy and processes for the Division/Directorate.

You will love this job if you:
  • Are a self-starter and require little oversight to complete given tasks
  • Enjoy a fast-paced work environment
  • Love working with diverse groups of individuals, including engineers and technicians
  • Are good at communicating with people
  • Have a positive attitude
  • Enjoy multitasking

Minimum requirements for this position:
  • Must possess a Bachelor's Degree in a technical, science or business discipline from an accredited* college/university and 6 years of experience in one of the following areas, as related to the respective job required: Communication, Logistics, Operations, Finance, Personnel/Human Resource Management, Program Management, Process Improvement, Safety, Security, and Environmental specialties; or an Associates Degree and 8 years of applicable experience in the assigned specialty area; or 10 years of experience performing the job duties in the assigned specialty area; or 10 years of military training in the specialty area, or a combination thereof, may be substituted for the education requirements.
  • Additional specialization requirements:
  • 4 years of the required experience must include experience coordinating projects; collecting data, reviewing technical documents compiling statistics and data for projects; writing narratives, managing the execution of inspection programs, creating, monitoring, and maintaining audit files for program compliance.
  • Knowledge with preparation of complete configuration documentation and overseeing the management of configuration items.
  • Experience with establishing and maintaining the consistency of a system's functional, performance and physical attributes with its requirements, design and operational information throughout a system's life cycle.
  • Experience with implementation of configuration control during development, test, production, delivery and sustainment of the products.
  • The Document Control Specialist should possess a strong knowledge of SOLIDWORKS® PDM.
  • Possess excellent written and verbal communication skills, proficiency in MS Office with the ability to work within a team environment.
  • Experience with controlling and tracking engineering changes to the product's technical baseline, ensuring thorough assessments of performance, cost and schedule impacts are completed prior to implementation.
  • Must be able to obtain and maintain a Secret Clearance (U.S. Citizenship is required for all applicants)

What we offer:
  • Competitive salaries.
  • Continuing education assistance.
  • Professional development allotment.
  • Multiple healthcare benefit packages.
  • 401K with employer matching.
  • Paid time off (PTO) along with federally recognized holiday schedule.