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Document Control Specialist Medical Device Jobs in Decatur, AL

RUAG

Document Control Specialist

Trinity, AL · On-site

Document Control Specialist Challenge the Impossible About Beyond Gravity Headquartered in Zurich, Switzerland, Beyond Gravity is not your typical space company. We're a unique blend of agility ...

New

Peraton

Asset Management Specialist

Huntsville, AL

$80K - $128K/yr

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 ...

Peraton

Asset Management Specialist

Huntsville, AL · On-site

$80K - $128K/yr

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 ...

Peraton

Asset Management Specialist

Huntsville, AL

$80K - $128K/yr

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 ...

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All JobsDocument Control Specialist Medical Device JobsDocument Control Specialist Medical Device Jobs in Decatur, AL

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 Aug 4, 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 does a document control specialist do?

A document control specialist in the medical device industry manages and maintains all documentation related to product development, quality systems, and regulatory compliance. They ensure documents are accurate, properly stored, and accessible, often using document management software, and support audits and inspections. Attention to detail and knowledge of industry standards like ISO 13485 are essential for this role.

What are the key skills and qualifications needed to thrive as a document control specialist in the medical device industry?

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.

Is document control a stressful job?

Document Control Specialists in the medical device industry often work in regulated environments that require attention to detail and compliance with standards like ISO 13485. The job can be demanding due to strict deadlines, audit preparations, and the need for accuracy, but it also offers structured workflows and clear procedures that help manage workload and reduce stress.

What is a document control specialist 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 Medical Device jobs near you

Document Control Specialist

RUAG

Trinity, AL • On-site

Other

Posted 3 days ago

New

Job description


Document Control Specialist

Challenge the Impossible

About Beyond Gravity

Headquartered in Zurich, Switzerland, Beyond Gravity is not your typical space company. We're a unique blend of agility, speed, and innovation, fusing a start-up mindset with decades of industry expertise and a track record of 100% mission success. Our dynamic team of over 1700 professionals, spread across 13 locations in six countries, is dedicated to pushing the boundaries of what is technically feasible. We're not just building crucial products for the satellites and launchers industry, we're helping to improve life on earth.

This position is responsible for supporting the execution of the Document Control activities in accordance with AS9100 and company quality standards and securing completed documentation.

Your Mission   

  • Responsible for supporting the execution of the Document Control activities in accordance with AS9100 and company quality standards, and securing completed documentation.
  • Review of all documents and data to be uploaded in to SAP (internal and customer facing) for completeness and accuracy and SAP functions in work order processing for production completion.
  • Complete all archiving activities for finalized documents.
  • Assist in writing and reviewing department procedures and SOPs.
  • Must be detail oreinted
  • Ability to pull and upload reports
  • Work on special projects for Production Control as needed.
  • Some weekend work may be needed to finalize paperwork as needed

Your Story

  • High school diploma or general education degree (GED)
  • Able to follow verbal and written instructions.
  • Able to deal with document ambiguity and reconcile missing information with relevant groups.
  • Able to work independently with minimal supervision in alignment to due dates.
  • Able to perform multiple activities for various projects in a fast-paced environment.
  • Strong personal computer skills required, including the use Microsoft Office.
  • SAP  database knowledge
  • Understanding of master data/configuration controls in a manufacturing environment
  • ERP system (SAP or similar) familiarity for recording and storing information in addition to document storage.

Are you ready for lift-off?

Our core values - Passionate, Together, and Curious - transform challenges into opportunities. Embark on a journey to transcend the ordinary with us. Propel your career to new heights by applying.We're actively reviewing candidates and will promptly select the ideal fit for our team. 

For questions regarding the position, please contact: Sherry Hester|sherry.hester@beyondgravity.com 
 

For questions regarding the position or recruitment process, please contact: Michelle Lach|michelle.lach@beyondgravity.com 

Beyond Gravity is proud to be an Equal Opportunity Employer. We welcome and encourage applications from all qualified individuals, regardless of race, color, religion, sex, gender, national origin, disability, protected veteran status, or any other legally protected categories. 

Applications by e-mail cannot be considered. We do not accept dossiers from recruitment agencies for this position. 

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