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Data Quality Control Manager Jobs in Boston, MA (NOW HIRING)

Data Quality Analysts Location: Boston, MA - Onsite Duration: Contract Overview We are seeking a ... Work on Trade Life Cycle and Management modules, including Front, Middle, and Back-office ...

Manage the pre-closing review process for Wholesale/Broker and Portfolio Retention loans in accordance with the Home Ownership Programs Lending Quality Control Plan * Review underwriting decisions ...

... data management foundation. At Cedar Gate, you'll be part of a collaborative, innovative ... Design and execute test plans, validation rules, regression testing, and quality control processes.

... data management foundation. At Cedar Gate, you'll be part of a collaborative, innovative ... Design and execute test plans, validation rules, regression testing, and quality control processes.

... data management foundation. At Cedar Gate, you'll be part of a collaborative, innovative ... Design and execute test plans, validation rules, regression testing, and quality control processes.

QC Microbiologist II

Hopkinton, MA ยท On-site

$74K - $85K/yr

Receive QC microbiological sample for internal testing, login, processing, tracking, distribution of test results, and closure * Assist QC management to author, review and approve documentation ...

QC Microbiologist II

Hopkinton, MA ยท On-site

$74K - $85K/yr

Receive QC microbiological sample for internal testing, login, processing, tracking, distribution of test results, and closure * Assist QC management to author, review and approve documentation ...

Support QC Microbiology Senior Manager in oversight of laboratory operations, technical initiatives ... Lead data trending and interpretation of environmental monitoring and microbiological data to ...

Quality Assurance Manager

Randolph, MA ยท On-site

$100K - $120K/yr

... QC Manager ensures all products meet stringent mechanical, electrical, and acoustic standards--particularly those required by hyperscale data center customers. This is a hands-on leadership role ...

Showing results 41-60

Data Quality Control Manager information

See Boston, MA salary details

$33.1K

$88.3K

$140.7K

How much do data quality control manager jobs pay per year?

As of Aug 22, 2026, the average yearly pay for data quality control manager in Boston, MA is $88,350.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,700.00 and $108,600.00 per year, depending on experience, location, and employer.

What does a data quality control manager do?

A Data Quality Control Manager is responsible for ensuring the accuracy, consistency, and reliability of data within an organization. They develop and implement data quality standards, monitor data processes, and coordinate with different teams to resolve data issues. Their work involves setting up quality assurance protocols, conducting audits, and using tools to track and improve data integrity. Their ultimate goal is to make sure that business decisions are based on high-quality, trustworthy data.

What are some common challenges data quality control managers face when implementing data governance policies across multiple departments?

Data Quality Control Managers often encounter challenges such as inconsistent data standards, resistance to new procedures, and varying levels of data literacy among departments. Successfully implementing data governance policies requires strong communication, clear documentation, and collaborative training sessions to align all stakeholders. Building trust and demonstrating the value of high-quality data can help gain buy-in and create a culture of accountability across the organization.

What are the key skills and qualifications needed to thrive as a data quality control manager, and why are they important?

To thrive as a Data Quality Control Manager, you need a strong background in data management, analytics, and quality assurance, often supported by a degree in information systems or a related field. Familiarity with data quality tools (such as Talend, Informatica, or SQL), data governance frameworks, and relevant certifications like CDMP is typically expected. Attention to detail, problem-solving abilities, and effective communication skills help you lead teams and collaborate across departments. These skills and qualifications are crucial for ensuring data integrity, supporting business decisions, and maintaining regulatory compliance.

What is the difference between Data Quality Control Manager vs Data Analyst?

AspectData Quality Control ManagerData Analyst
Primary FocusOverseeing data quality standards, implementing quality control processesAnalyzing data to identify trends, generate reports, and support decision-making
Required SkillsData management, quality assurance, attention to detailData analysis, statistical skills, data visualization
Work EnvironmentQuality assurance teams, data management departmentsBusiness units, analytics teams, IT departments
Common CertificationsCertified Data Management Professional (CDMP), Six SigmaNone typically required, but certifications like Microsoft Data Analyst Associate are beneficial

The Data Quality Control Manager primarily focuses on maintaining and improving data quality standards within an organization, ensuring data accuracy and consistency. In contrast, a Data Analyst interprets data to provide insights and support strategic decisions. While both roles require strong data skills, the manager emphasizes quality assurance processes, whereas the analyst emphasizes data interpretation and reporting.

What are popular job titles related to Data Quality Control Manager jobs in Boston, MA?

For Data Quality Control Manager jobs in Boston, MA, the most frequently searched job titles are:

Infographic showing various Data Quality Control Manager job openings in Boston, MA as of August 2026, with employment types broken down into 14% Internship, 72% Full Time, and 14% Contract. Highlights an 100% In-person job distribution, with an average salary of $88,350 per year, or $42.5 per hour.

Director, Quality Control

Sebela Pharmaceuticals Inc.

Holbrook, MA โ€ข On-site

Full-time

Re-posted 12 days ago


Job description

Sebela Pharmaceuticals is a U.S. pharmaceutical company with a market-leading position in Gastroenterology and a focus on innovation in Womenโ€™s Health. Our Vision is to build the leading Gastroenterology company in the U.S., with a complementary
focus on innovation in Womenโ€™s Health, premised on our expertise in pharmaceutical development and commercialization. Braintree Laboratories, Inc., a part of Sebela Pharmaceuticals, has its contract development and manufacturing organization (CDMO) in Holbrook, MA, offering pharmaceutical-development and in-house manufacturing services for specialty gastroenterology products.
We value dedication, energy, and enthusiasm, and we focus on innovation and results while striving to achieve our corporate mission and vision. Sebela Pharmaceuticals is committed to cultivating an inclusive environment where all employees are treated with respect. We accomplish this by fostering a culture of diversity, equity and inclusion, which is essential to innovation and continuous improvement. Sebela operates from three locations in Roswell, Georgia, Braintree and Holbrook, MA and headquarters in Dublin, Ireland.
This position is responsible for leading Quality Controls Laboratory operations at the Holbrook site including the development, implementation and maintenance of quality control systems and activities to support commercial manufacturing and new product introductions.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
  • Provide strategic leadership and oversight of QC operations, ensuring alignment with company objectives for product quality, regulatory compliance, and business performance.
  • Direct all QC laboratory activities, in support of GMP Testing, release, and stability programs, including laboratory safety, testing operations, resource allocation, and performance management.
  • Review and approve QC specifications, procedures, protocols, validation documents, and analytical methods related to raw materials, intermediates, and commercial products.
  • Ensure all testing is performed in accordance with internal procedures and cGMP requirements.
  • Lead investigations into Out-of-Specification (OOS) results and laboratory deviations ensuring timely root cause identification and implementation of effective corrective and preventive actions (CAPAs).
  • Maintain inspection readiness across QC operations, supporting regulatory inspections, customer audits, and internal quality audits.
  • Oversee laboratory change control processes, risk assessments, equipment qualification activities, and implementation of compliant operational improvements.
  • Ensure critical laboratory equipment is appropriately qualified, calibrated, maintained, and operated to support reliable testing and maintain data integrity.
  • Ensure laboratory data integrity, documentation accuracy, and adherence to ALCOA principles
  • Partner with Quality Assurance, Manufacturing, and external stakeholders to investigate product quality issues and drive continuous improvement initiatives.
  • Lead supplier quality support activities, including supplier qualification, performance monitoring, and resolution of supplier-related quality issues.
  • Monitor and analyze QC performance metrics and quality system trends to identify risks, drive operational excellence, and strengthen compliance.
  • Develop, mentor, and retain a high-performing QC organization, fostering a culture of accountability, collaboration, and continuous professional development.
  • Manage departmental budgets, capital planning, and resource requirements to ensure effective execution of business and quality objectives.
  • Other duties as assigned.
KEY COMPETENCIES:
  • Leadership and teamwork
  • Regulatory Compliance, cGMP, Statistical Process Control
  • Extensive analytical chemistry experience
  • Project management
  • Data collection, management and analysis
  • Ability to direct and be resilient and focused under pressure
  • Planning and time management
  • Strong decision-making skills
  • Ability to manage multiple priorities
  • Ability to foster excellent working relationships across all levels, internal/external customers and suppliers
QUALIFICATIONS:
To perform this job successfully, an individual must be able to perform each essential function satisfactorily, be flexible in terms of work hours, and have strong knowledge and experience in cGMPs and Oral Dose Pharmaceutical Production Processes. The requirements listed below are representative of the knowledge, skills and/or abilities required.
  • BS or masterโ€™s degree in chemistry, biology, or other pharmaceutical science related field.
  • Minimum of 8-10 years QC management experience working in pharmaceutical finished product manufacturing with experience in compliance, quality control, and regulatory development.
  • Direct experience interacting with FDA and other regulatory agencies.
  • Strong knowledge and understanding of FDA cGMP regulations.
  • Experienced in GMP audits, including drug product manufacturing and analytical testing sites.
  • Ability to build collaborative relationships and lead effectively in a cross-functional environment.
  • Self-motivated and results-driven leader with a proactive, hands-on approach.
  • Strong organizational, prioritization, and time management skills, coupled with strong critical-thinking abilities to evaluate complex challenges, solve problems effectively, and drive continuous improvement.
  • Strong project management skills.
  • Excellent written and oral communication / presentation skills.
  • Adept at and comfortable with statistical analysis.
Pay Range: $150-190K base (this reflects our reasonable and good faith estimate of what will be paid at the time of posting). Competitive benefits package included.