ZipRecruiter

Log In

1

Document Control Manager Jobs in Canton, MA (NOW HIRING)

Nova Biomedical

Sr. QC Manager

Waltham, MA · On-site

The Sr. Quality Control Manager is responsible for leading and scaling Quality Control (QC) ... Oversee the management of documentation, records, test reports, deviations, investigations, CAPAs ...

Nova Biomedical

Sr. QC Manager

Waltham, MA · On-site

The Sr. Quality Control Manager is responsible for leading and scaling Quality Control (QC) ... Oversee the management of documentation, records, test reports, deviations, investigations, CAPAs ...

Nova Biomedical

Sr. QC Manager

Waltham, MA

The Sr. Quality Control Manager is responsible for leading and scaling Quality Control (QC) ... Oversee the management of documentation, records, test reports, deviations, investigations, CAPAs ...

Aramark

Inventory Control Manager

Boston, MA · On-site

$70K - $80K/yr

The Inventory Control Manager is to oversee the purchasing, receiving, and accounts payable ... and receiving documents. * Supports the daily management and continuous improvement of the ...

Aramark

Inventory Control Manager

Boston, MA · On-site

$70K - $80K/yr

The Inventory Control Manager is to oversee the purchasing, receiving, and accounts payable ... and receiving documents. * Supports the daily management and continuous improvement of the ...

Aramark

Inventory Control Manager

Boston, MA · On-site

$70K - $80K/yr

The Inventory Control Manager is to oversee the purchasing, receiving, and accounts payable ... and receiving documents. * Supports the daily management and continuous improvement of the ...

Aramark

Inventory Control Manager

Boston, MA

$70K - $80K/yr

The Inventory Control Manager is to oversee the purchasing, receiving, and accounts payable ... and receiving documents. * Supports the daily management and continuous improvement of the ...

American Society for Quality

Sr. QC Manager

Waltham, MA · On-site

$150 - $170/hr

Oversee the management of documentation, records, test reports, deviations, investigations, CAPAs ... Experience linking QC trends, nonconformances, complaint investigations, and manufacturing ...

Kelly Services

Quality Control Manager

Mansfield, MA

$100K - $110K/yr

This role manages the quality team, oversees testing, supplier quality, customer issues, and ... Maintain quality procedures, specifications, and documentation to support compliance and ...

New

Cox Engineering

Quality Assurance Manager

Randolph, MA · On-site

$100K - $120K/yr

Maintain and manage document control, revision control, and record retention for all quality documentation. * Lead semi-annual Management Reviews and report quality performance to executive ...

previous pagenext page

Showing results 21-40

All JobsDocument Control JobsDocument Control Manager JobsDocument Control Manager Jobs in Canton, MA

Document Control Manager information

See Canton, MA salary details

$37K

$104.6K

$167.1K

How much do document control manager jobs pay per year?

As of Aug 16, 2026, the average yearly pay for document control manager in Canton, MA is $104,620.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,200.00 and $124,800.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a document control manager?

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.

Is document control a good career path?

A career as a Document Control Manager involves overseeing the organization, accuracy, and accessibility of company documents, often requiring skills in document management software and attention to detail. It can offer stable employment opportunities in industries like construction, manufacturing, and engineering, with potential for advancement into project management or quality assurance roles.

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.

More about Document Control Manager jobs

What cities near Canton, MA are hiring for Document Control Manager jobs?

Cities near Canton, MA with the most Document Control Manager job openings:

Document Control Manager jobs near you
Infographic showing various Document Control Manager job openings in Canton, MA as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 13% Part Time, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $104,620 per year, or $50.3 per hour.

Sr. QC Manager

Nova Biomedical

Waltham, MA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 26 days ago

Job description

Nova Biomedical: One Global Brand. One Vision. Together under one name.
Advanced Instruments and Nova Biomedical are now united under one brand, Nova Biomedical, marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we're accelerating innovation, supporting critical workflows, and delivering world-class service across the biopharmaceutical and clinical markets.
Job Summary:
The Sr. Quality Control Manager is responsible for leading and scaling Quality Control (QC) operations across multiple U.S. manufacturing facilities in Waltham, Norwood, and Billerica, Massachusetts, supporting the production of biotechnology and clinical systems, including point-of-care (POC) and in vitro diagnostic (IVD) medical devices, consumables, and reagents.
This role ensures product quality, regulatory compliance, and operational excellence throughout the manufacturing lifecycle, with a strong emphasis on data-driven quality management, statistical monitoring, and continuous improvement. The Sr. Quality Control Manager will develop and execute comprehensive quality control strategies that support FDA medical device requirements, MDSAP, IVDR, ISO 13485, ISO 14971, and other applicable regulatory standards while enabling scalable growth across the organization.
The ideal candidate will be a collaborative leader who partners closely with Manufacturing, Quality Assurance, Regulatory Affairs, R&D, and Operations leadership to drive quality objectives, business expansion, and commercialization goals.
Responsibilities:
  • Lead Quality Control functions across multiple manufacturing and distribution sites within the United States.
  • Establish and maintain enterprise-wide QC strategies, policies, procedures, and performance metrics.
  • Build, develop, and mentor high-performing Quality Control teams while fostering a culture of accountability, compliance, and continuous improvement.
  • Ensure consistency of QC practices, testing methodologies, and inspection standards across all facilities.
  • Drive operational excellence initiatives that improve product quality, efficiency, and scalability.
  • Establish robust systems for collecting, monitoring, analyzing, and reporting product quality and manufacturing performance data.
  • Proactively identify trends, emerging product risks, recurring defects, process shifts, and performance gaps to support continuous improvement.
  • Lead root cause investigations using structured problem-solving methodologies and statistical tools.
  • Analyze quality, yield, reliability, complaint, nonconformance, and production output data to improve product performance and manufacturing capability.
  • Ensure compliance with FDA, MDSAP, IVDR, ISO, and other applicable regulatory requirements and harmonized standards.
  • Oversee the management of documentation, records, test reports, deviations, investigations, CAPAs, and quality metrics.
  • Collaborate with R&D, Supplier Quality, Incoming Inspection, Manufacturing, Manufacturing Engineering, Finished Goods, and Distribution teams to drive quality improvements.
  • Support engineering and manufacturing quality initiatives through the effective use of procedures, processes, quality engineering tools, and data analysis.

Experience Requirements:
  • Bachelor's degree or higher in a technical discipline, preferably within Life Sciences, Chemistry, Medical Technology, or a related field.
  • 5-10+ years of Quality Control management experience within an FDA-regulated medical device, IVD, or reagent manufacturing environment.
  • Strong working knowledge of ISO 13485, ISO 14971, MDSAP, IVDR, and FDA regulations including 21 CFR Part 820.
  • Experience developing product and process trend analyses, nonconformance reduction programs, risk reduction initiatives, cost containment efforts, and executive-level quality reporting.
  • Experience applying product lifecycle risk management principles for IVD medical devices.
  • Experience linking QC trends, nonconformances, complaint investigations, and manufacturing performance data to product risk management activities.
  • Experience with process and equipment validation activities, including authoring and reviewing IQ, OQ, and PQ documentation.
  • Experience authoring Quality Plans and Quality Control Plans.
  • Experience supporting multi-site manufacturing operations.
  • Strong project management, leadership, and team development skills.
  • ASQ Certified Manager of Quality/Organizational Excellence (CMQ/OE), ASQ Certified Quality Engineer (CQE), and/or Green Belt Six Sigma certification preferred.

Physical Requirements and Working Conditions:
  • Comfort with working at a computer for extended periods.
  • Capacity to lift and carry up to [25-50] pounds as required
  • Able to communicate effectively via phone, video, and written communication.
  • Occasional need to move about the office to access meetings or resources.

Why Work for Nova Biomedical
  • Flexible Medical, Dental, & Vision Coverage
  • Competitive 401k company match
  • Bonus Program, Generous PTO and paid holidays
  • Generous Tuition reimbursement
  • Hybrid and flexible work arrangements
  • Professional development, engagement and events
  • Company marketplace for lunch and snacks in our Norwood, MA, Billerica, MA and Westbrook, ME offices
  • Company subsidized cafeteria in our Waltham, MA office

Work Location: Waltham, MA
Targeted Salary Range: $150,000-$170,000/yr
Nova Biomedical believes in transparency and integrity throughout all we do, including compensation. The provided salary range for this role represents the expected base salary or hourly rate for this opening. Actual compensation will be commensurate with the candidate's experience and may vary based on individual factors such as location, skills, and education.
About the Company
At Nova Biomedical, we're not just building instruments, we're powering breakthroughs that improve lives. Our smart, science-driven solutions are trusted in over 100 countries to speed drug development and enhance patient care.
Our integration brings together more than 70 years of scientific excellence with Nova's cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA-registered, ISO-certified manufacturing, more than 125 FDA approvals, and industry-trusted diagnostics, we're setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences.
With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we're building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity.
Working at Nova Biomedical means joining a mission-driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, you'll be part of a team that values innovation, invests in your growth, and is committed to making a real-world impact on global health.
Explore what's next with us at novabiomedical.com
EEO Statement:
Nova Biomedical takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce. As a part of our commitment to a diverse and inclusive workforce, Nova Biomedical will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.
Privacy Policy
https://advancedinstruments.showpad.com/share/DmsEd5QTLlqemTYABlvDW

Apply