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Document Control Specialist Medical Device Jobs in Decatur, AL

Nordson Corporation

Assembler I

Arab, AL · On-site

$16.25 - $20/hr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

Nordson Medical , a global leader in Interventional Solutions, Fluid Components, and Surgical ... Complete all required daily documentation whether manual or electronically * Keep work area clean ...

Nordsonhcm

Assembler I

Arab, AL

$16.25 - $20/hr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

Nordson Medical , a global leader in Interventional Solutions, Fluid Components, and Surgical ... Complete all required daily documentation whether manual or electronically * Keep work area clean ...

Yulista

Inventory Control I

Huntsville, AL · On-site

$17.75 - $23/hr

Responsible for control and accuracy of material and records using both manual and electronic ... Ability to read and interpret documents such as safety rules, operating and maintenance ...

Yulista

Inventory Control I

Huntsville, AL · On-site

$17.75 - $23/hr

Responsible for control and accuracy of material and records using both manual and electronic ... Ability to read and interpret documents such as safety rules, operating and maintenance ...

Yulista

Inventory Control I

Huntsville, AL · On-site

$17.75 - $23/hr

Responsible for control and accuracy of material and records using both manual and electronic ... Ability to read and interpret documents such as safety rules, operating and maintenance ...

Yulista

Inventory Control I

Huntsville, AL · On-site

$17.75 - $23/hr

Responsible for control and accuracy of material and records using both manual and electronic ... Ability to read and interpret documents such as safety rules, operating and maintenance ...

Yulista

Inventory Control I

Huntsville, AL · On-site

$17.75 - $23/hr

Responsible for control and accuracy of material and records using both manual and electronic ... Ability to read and interpret documents such as safety rules, operating and maintenance ...

COLSA Corporation

Cyber AI Specialist

Huntsville, AL · On-site

General Summary COLSA is seeking a highly skilled Cyber AI Specialist with deep expertise in ... Support RMF activities across all phases, including documentation, control implementation, security ...

Teledyne

Configuration Manager

Huntsville, AL · On-site

... medical imaging and pharmaceutical research. We are looking for individuals who thrive on making an ... Administer document control processes to ensure proper creation, review, approval, release ...

Teledyne FLIR LLC

Configuration Manager

Huntsville, AL · On-site

... medical imaging and pharmaceutical research. We are looking for individuals who thrive on making an ... Administer document control processes to ensure proper creation, review, approval, release ...

MSSI

Medical Logistics Specialist (D)

Huntsville, AL · On-site

Medical Logistics Specialist Multiple locations may include: Guantanamo Bay, Cuba, Chicago, IL ... related documentation and records • Comply with local, state, and federal laws regarding ...

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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 17, 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 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 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 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 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 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 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

Documentation Specialist

Applied Technologies Group, Inc.

Huntsville, AL • On-site

Other

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 13 days ago

Job description

Who We Are: AM Pierce & Associates and Applied Technologies Group (ATG), a wholly owned subsidiary of AM Pierce and Associates, is a woman-owned small business providing Engineering & Research, Cyber, C5ISR, Program & Acquisition Management services and solutions to a diverse government and industry client base. We are a stable and growing company who offers our employees a rich benefits package, supportive and flexible work environment, and the opportunity to work with experts in their field.
The Position: We are looking for a candidate who will be performing the role of Documentation Specialist, supporting the Utility Helicopter Project Office (UHPO).
The Location: Redstone Arsenal, AL
The Work Environment: On-Site
The Description:
The Documentation Specialist will be a key member of the Logistics Management Division, providing critical support to the Utility Helicopters Project Office. This role is central to ensuring the accuracy, completeness, and compliance of all logistics-related documentation throughout the system's lifecycle.
Duties Include:
  • Develop, update, and maintain essential logistics documentation including the Lifecycle Sustainment Plan (LCSP) and required LCSP annexes. Additional documentation required may include but are not limited to Level of Repair Analysis (LORA), Depot Maintenance Support Plan (DMSP), Item Unique Identification (IUID) plans, and Transition to Sustainment (T2S) documents.
  • Prepare comprehensive documentation packages and briefing materials for formal program milestones and Sustainment Reviews.
  • Coordinate and facilitate the staffing and review of logistics documents with a wide range of internal and external organizations, ensuring all stakeholder feedback is incorporated.
  • Track and manage document versions, revisions, and approvals using established configuration management processes.
  • Ensure all documentation adheres to stringent Department of War (DoW), Department of the Army (DA) and defense acquisition regulations and standards.
  • Assist in the analysis and integration of logistics requirements into program and design specifications.
Education & Experience:
  • Active DoD Secret Clearance, required.
  • Bachelor's degree in a related field with at least eight (8) years of related experience.
    • ALLOWABLE SUBSITIUTIONS:
      • PhD with four (4) years of related experience.
      • Masters's degree with six (6) years of related experience.
      • Associate's degree with ten (10) years of related experience.
      • High School Diploma/GED with twelve (12) years of related experience.
    • Strong background in logistics management and technical documentation within the defense acquisition community.
    • Experience developing, writing, and editing technical and logistics documentation for DoD acquisition programs.
    • Proven ability to interpret and apply DoD instructions and standards to program documentation.
    • Experience coordinating with diverse teams, including engineering, finance, and program management, to gather information and facilitate document reviews.
    • Familiarity with the structure and content requirements of key acquisition documents, such as the Lifecycle Sustainment Plan (LCSP).
    • Hands-on experience with document management systems and collaboration tools.
    • Exceptional written and verbal communication skills, with a proven ability to produce clear, concise, and accurate documentation.
    • Strong organizational and time-management skills, with the capacity to manage multiple priorities and deadlines effectively.
    • Meticulous attention to detail and a commitment to quality control.
    • Proficiency in the Microsoft Office Suite (Word, Excel, PowerPoint, Teams).
Desired Skillset:
  • Familiarity with defense acquisition terminology and the roles of various DoD logistics and materiel commands.
  • Ability to think critically and analytically to resolve documentation issues and discrepancies.
  • A collaborative and solution-oriented mindset, with the ability to work effectively both independently and as part of a team.
Travel:
  • The employee will be expected to travel up to 10% of the time.
AM Pierce & Associates, as well as its subsidiaries, invests in its employees beyond just compensation. Elements of the Total Rewards package include competitive base pay and variable compensation opportunities. AM Pierce & Associates, as well as its subsidiaries, also provides eligible employees with an opportunity to enroll in a variety of benefit programs, generally including:
  • Medical, Dental and Vision Insurance
  • Life and Accidental Death & Disability Coverage
  • Traditional 401(k) and ROTH 401(k) Retirement Plans
  • Paid Time Off and Holidays
  • Professional Development Opportunities
  • Incentive Programs, Awards and Recognition
  • Employee Assistance Program
  • Will Preparation
  • Identity Theft Protection & Legal Support
  • Referral Program
  • Voluntary Accident, Critical Illness, and Hospital Indemnity Coverage
  • Pet Insurance
  • Norton Life Lock
  • HSA and FSA plans

The specific program and options available to any given employee may vary depending on eligibility factors such as geographic location, date of hire, Full or Part-time status, and the applicability of collective bargaining agreements.
For all positions requiring access to technology/software source code that is subject to export control laws, employment with the company is contingent on either verifying U.S.-person status or obtaining any necessary license. The applicant will be required to answer certain questions for export control purposes, and that information will be reviewed by compliance personnel to ensure compliance with federal law. AM Pierce & Associates, as well as its subsidiaries may choose not to apply for a license for such individuals whose access to export-controlled technology or software source code may require authorization and may decline to proceed with an applicant on that basis alone.
AM Pierce and Associates, Inc. and Applied Technologies Group, Inc., a wholly owned subsidiary of AM Pierce and Associates, Inc., are Equal Opportunity Employers. It is the policy of AM Pierce & Associates, Inc. and Applied Technologies Group, Inc. not to discriminate or allow the harassment of employees. All applicable laws are followed to ensure all qualified applicants are employed, and employees are treated during employment, without regard to their sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected veteran status, or any other characteristic protected by applicable federal, state, local, or international law.
If you require reasonable accommodations to apply for a position with AM Pierce & Associates, as well as its subsidiaries, through its online applicant system, please contact AM Pierce & Associates Human Resources Department at (240) 718-3800 or email us at hr@ampierce.com.
If your background meets the qualifications of the position, please submit your resume and salary requirements to careers@ampierce.com or submit an application online.
AM Pierce & Associates, as well as its subsidiaries, verifies employment eligibility through E-Verify.
This is a non-management position.

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