2

Remote Iso Document Control Jobs in Massachusetts

$130K - $140K/yr

Role Overview The Manager, Document Control and Training will support the end-to-end Document ... Position Location This is a remote role; periodic travel to team and company events is required.

You just found it. Job Overview Responsible for the generation and development of documents ... ISO 13485 and ISO14971) * Demonstrated ability to work independently and as part of a team.

You just found it. Job Overview Responsible for the generation and development of documents ... ISO 13485 and ISO14971) * Demonstrated ability to work independently and as part of a team.

Remote Job Type: Contractor Pay: $60-$65/hour Job Overview We are looking for an experienced ... TFL production & QC * Regulatory submissions & CSR review * Strong documentation, communication ...

Remote Job Type: Contractor Pay: $60-$65/hour Job Overview We are looking for an experienced ... TFL production & QC * Regulatory submissions & CSR review * Strong documentation, communication ...

We are open to remote, hybrid or in-office work schedules. The P&C Designer reports to our P&C ... Lead/Support Document Control functions including ProjectWise management, drawing requests, drawing ...

next page

Showing results 1-20

Remote Iso Document Control information

What is the difference between Remote Iso Document Control vs Remote Quality Document Control?

AspectRemote Iso Document ControlRemote Quality Document Control
CertificationsISO standards knowledge, document management certificationsQuality management system certifications, document control certifications
Work EnvironmentPrimarily office or remote, industry-specificPrimarily office or remote, industry-specific
Industry UsageManufacturing, engineering, aerospaceManufacturing, healthcare, automotive
Search & ComparisonOften compared for ISO compliance rolesCompared for quality assurance roles

Remote Iso Document Control focuses on managing documents related to ISO standards compliance, ensuring proper documentation for certifications and audits. Remote Quality Document Control emphasizes maintaining quality management system documents across various industries. While both roles involve document management, Iso Document Control is more specialized in ISO standards, whereas Quality Document Control covers broader quality processes.

What are the most commonly searched types of Iso Document Control jobs in Massachusetts?

The most popular types of Iso Document Control jobs in Massachusetts are:

What cities in Massachusetts are hiring for Remote Iso Document Control jobs?

Cities in Massachusetts with the most Remote Iso Document Control job openings:

Infographic showing various Remote Iso Document Control job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 19% Part Time, and 5% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Specialist, QMS - Document Control

Amylyx Pharmaceuticals

Cambridge, MA • On-site, Remote

Full-time

Posted 17 days ago


Job description

The Opportunity

The Specialist, Quality Management Systems (QMS) - Document Control is responsible for the administration, maintenance, and continuous improvement of the organization's document control processes within the Quality Management System. This role ensures the effective lifecycle management of controlled documents and records in compliance with applicable GxP regulations, company policies, and industry standards.

The Specialist serves as a key business partner to cross-functional teams, supporting the creation, review, approval, distribution, training, and archival of controlled documents while maintaining inspection readiness and promoting operational excellence across the organization.

Responsibilities

  • Document Control Management
    • Administer document control processes within the eQMS, ensuring effective lifecycle management of controlled documents and records in compliance with quality and regulatory requirements.
  • eQMS Administration and Support
    • Serve as the subject matter expert for document control processes within the eQMS, providing system administration, user support, and continuous improvement of document management functionality.
  • Training Management and Compliance
    • Coordinate and maintain document-related training activities and records to ensure compliance with quality system and regulatory requirements.
  • Compliance and Inspection Readiness
    • Ensure document control and records management processes support compliance with applicable regulations, quality standards, and audit/inspection readiness requirements.
  • Metrics, Continuous Improvement, and QMS Support
    • Monitor document control performance, identify improvement opportunities, and support initiatives that enhance QMS effectiveness, compliance, and operational efficiency.

Required Qualifications

  • Bachelor's degree
  • 1-3 years in pharmaceutical/biotech Quality (GMP environment)
  • Experience managing controlled documents and records within an electronic Quality Management System (eQMS), including experience with Veeva Vault Quality Docs/Veeva Vault Quality.
  • Working knowledge of Quality Management Systems (QMS), document control principles, records management, and Good Documentation Practices (GDocP).
  • Understanding of GxP regulations, data integrity requirements, and industry standards applicable to biopharmaceutical organizations.
  • Experience supporting quality audits, regulatory inspections, and compliance activities in a regulated environment.
  • Strong attention to detail, organizational skills, and ability to manage multiple priorities while meeting deadlines.
  • Strong analytical, problem-solving, written, and verbal communication skills, with the ability to work effectively across cross-functional teams.
  • Proficiency in Microsoft Office applications (Word, Excel, PowerPoint, and Teams).

Preferred Requirements

  • Certification in Quality, Records Management, or a related discipline.
  • Experience supporting eQMS implementation, validation, system administration, or continuous improvement initiatives.

Work Location and Conditions

  • At Amylyx, we proudly support remote work opportunities within the United States. However, due to business considerations related to health insurance coverage and state tax regulations, we are unable to hire employees who reside and/or work in certain states. Currently, we are not considering applicants from Alaska, Arizona, Hawaii, Michigan and Tennessee.
  • You will be expected to travel to our corporate location in Cambridge, MA several times a year and attend other company-related events as necessary and requested.
  • You must have access to work in setting which enables meeting all requirements of the role (including privacy, reliable internet access, phone, ability to video conference, etc.) at your remote location.