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Remote Quality Control Inspector Jobs in Boston, MA

Valspec

QA Consultant

Boston, MA · Remote

Remote Employment Type: Contract / Consulting (6-12+ months) Start Date: ASAP About the Role: We ... Support audit readiness and inspection preparedness activities * Assist with implementation and ...

SQA Services

Quality Auditor - Pharmaceutical

Boston, MA · Remote

$1.30K/day

For nearly 30 years, SQA Services has been a leading provider of managed supplier quality services, offering audits, assessments, remote surveillance, corrective actions, remediation, inspections ...

Aggreko

Project Site Manager

Boston, MA · Remote

$80K - $110K/yr

Strong knowledge of construction safety standards, QA/QC practices, and project controls ... Willingness to travel and work on remote or international project sites as required. (50 ...

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How much do remote quality control inspector jobs pay per hour?

As of May 30, 2026, the average hourly pay for remote quality control inspector in Boston, MA is $23.33, according to ZipRecruiter salary data. Most workers in this role earn between $18.80 and $26.11 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Remote Quality Control Inspector, and why are they important?

To thrive as a Remote Quality Control Inspector, you need expertise in inspection techniques, quality standards, and documentation, often supported by experience in manufacturing or related certifications such as ISO 9001. Familiarity with digital inspection tools, quality management systems (QMS), and video conferencing platforms is typically required. Strong attention to detail, critical thinking, and effective communication skills help you identify issues and collaborate with remote teams. These skills are crucial to ensuring product quality and compliance while maintaining efficiency in a remote work environment.

How does a Remote Quality Control Inspector effectively communicate and coordinate with on-site teams?

Remote Quality Control Inspectors rely heavily on digital communication tools such as video calls, instant messaging, and project management platforms to stay connected with on-site staff. They frequently review photographic or video evidence, provide feedback, and clarify inspection standards in real time to ensure product quality. Regular virtual meetings and clear documentation are essential to address any issues quickly and maintain alignment with project timelines. Building strong remote relationships and being proactive in communication help overcome the challenge of not being physically present.

What are Remote Quality Control Inspectors?

Remote Quality Control Inspectors are professionals who assess and monitor the quality of products, services, or processes without being physically present at a manufacturing site or facility. They use digital tools, cameras, and specialized software to evaluate compliance with quality standards, identify defects, and ensure that products meet company and regulatory requirements. This role is increasingly common in industries where remote monitoring and digital documentation are feasible, enabling quality checks from virtually anywhere. Remote inspectors often collaborate with on-site teams to address issues and ensure continuous improvement. Their work helps maintain high-quality standards while reducing travel and operational costs.

What is the difference between Remote Quality Control Inspector vs Remote Quality Assurance Specialist?

AspectRemote Quality Control InspectorRemote Quality Assurance Specialist
CertificationsISO, Six Sigma, or industry-specific quality certificationsISO, Six Sigma, or quality management certifications
Work EnvironmentInspecting products, reviewing documentation remotely, analyzing dataDeveloping quality processes, auditing, ensuring compliance remotely
Industry UsageManufacturing, production, supply chainManufacturing, software, service industries
Search IntentRemote QC inspector jobs, quality control rolesRemote QA specialist roles, quality assurance jobs

While both roles focus on quality, the Remote Quality Control Inspector primarily conducts inspections and reviews products or processes remotely to identify defects. The Remote Quality Assurance Specialist develops and maintains quality systems, audits processes, and ensures compliance. Both roles require similar certifications and are used across manufacturing and service industries, but their core responsibilities differ in focus and scope.

What are the most commonly searched types of Quality Control Inspector jobs in Boston, MA? The most popular types of Quality Control Inspector jobs in Boston, MA are:
What are popular job titles related to Remote Quality Control Inspector jobs in Boston, MA? For Remote Quality Control Inspector jobs in Boston, MA, the most frequently searched job titles are:
What job categories do people searching Remote Quality Control Inspector jobs in Boston, MA look for? The top searched job categories for Remote Quality Control Inspector jobs in Boston, MA are:
What cities near Boston, MA are hiring for Remote Quality Control Inspector jobs? Cities near Boston, MA with the most Remote Quality Control Inspector job openings:
Remote Quality Control Inspector jobs near you
Senior Manager, Clinical Quality Assurance

Senior Manager, Clinical Quality Assurance

Deciphera Pharmaceuticals

Waltham, MA • On-site, Remote

$138K - $190K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 2 days ago

Job description

Company Description
Job Description
The Senior Manager, Clinical Quality Assurance is responsible for the development, maintenance and oversight of GCP activities related to the Clinical Trial activities sponsored by Deciphera. The primary responsibilities are to ensure both quality and compliance of Deciphera sponsored clinical trials with respect to Standard Operating Procedures, applicable regulatory requirements (US FDA, ICH, and country specific), along with current industry standards and practices.
Key Responsibilities
Clinical Quality Support 50%
  • Draft, review or revise Clinical QA SOPs to assess consistency and compliance with regulatory requirements/internal standards
  • Attend cross-functional team meetings and provide guidance to clinical operations staff based on interpretation of current regulations to ensure best practices including risk-based management
  • Work closely with Clinical Operations to ensure/coordinate appropriate and complete resolution of findings/non-compliant issues, quality investigations, etc. in a timely manner, including approval of corrective action and preventative action (CAPA) plans, as necessary
  • Provide Quality Control (QC) review of clinical protocols, amendments, Informed Consent Forms, Clinical Study Reports and other clinical trial related documents
  • Assist and advise with training QA and clinical staff as necessary for GCP
  • Identify potential systemic gaps and coordinate with the appropriate stakeholder to ensure timely remediation
  • As appropriate, escalate issues of critical non-compliance and/or lack of urgency in remediation to senior management via the Quality Board
  • Perform program specific root cause analysis of compliance issues and provide the appropriate metrics for tracking and trending for the overall QA reporting requirements to functional and senior management

Audit Planning and Oversight 40%
  • Conduct and/or assist in internal audits (systems, processes, vendors, computer system validation)
  • Interact with contract auditors in the scheduling process, kick-off meetings with auditors and internal groups, assist in the drafting of audit plans, confirmation letters and agendas, etc.
  • Identify the need for, conduct and/or assist in external audits (includes, but is not limited to, investigator sites, central IRBs, CROs and clinical labs)
  • Oversee the audit response process for the Investigator Site and Contract Research Organization (CRO) audits/inspections and ensure acceptability of actions to address findings through the CAPA process

Inspections 10%
  • Assist with inspection readiness, and regulatory inspections as needed

Other duties and responsibilities as assigned
Qualifications
Required Qualifications
  • 8+ years of direct GCP pharmaceutical/biotechnology experience with Bachelors degree or equivalent
  • Solid understanding and application of GCP, GLP and ICH requirements, especially ICH E6R3
  • A well organized, self-motivated and independent work style with the ability to initiate and follow through on assignments
  • Excellent interpersonal skills with knowledge of basic negotiation, influencing and conflict management to assure effective interactions within and across departments
  • The ability to simultaneously handle multiple project issues while dealing with time demands, incomplete information, or unexpected events
  • Broad experience in product development, clinical operations, regulatory compliance and GCP auditing
  • Willingness to travel up to 25% both domestic and international

Additional Information
Deciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $138,000 - $190,000. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location.
Deciphera believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Deciphera's competitive total rewards strategy that also includes annual performance bonus, a long-term incentive plan, full range of benefits and other incentive compensation plans (if applicable)
Benefits:
  • Competitive salary and annual bonus.
  • Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match, and more.
  • Generous parental leave and family planning benefits.
  • Outstanding culture and opportunities for personal and professional growth.

Apply Now: Join us in our mission to improve the lives of people with cancer. Apply today to become a part of our dynamic team!
EQUAL EMPLOYMENT OPPORTUNITY INFORMATION
Deciphera is committed to equal employment opportunity and values diversity. To ensure that we comply with reporting requirements, we invite you complete the confidential survey at the end of this application. Providing this information is optional. It will not be accessible or used in the hiring process, and has no effect on your opportunity for employment. This information will also be treated confidentially. We are committed to make all hiring decisions and other employment decisions on a non-discriminatory basis.
EQUAL EMPLOYMENT OPPORTUNITY INFORMATION
Deciphera is committed to equal employment opportunity and values diversity. To ensure that we comply with reporting requirements, we invite you complete the confidential survey at the end of this application. Providing this information is optional. It will not be accessible or used in the hiring process, and has no effect on your opportunity for employment. This information will also be treated confidentially. We are committed to make all hiring decisions and other employment decisions on a non-discriminatory basis.

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