ZipRecruiter

Log In

1

Quality Control In Jobs in Sutton, MA (NOW HIRING)

American Society for Quality

Sr. QC Manager

Waltham, MA · On-site

$150 - $170/hr

S. manufacturing facilities in Waltham, Norwood, and Billerica, Massachusetts, supporting the ... The Sr. Quality Control Manager will develop and execute comprehensive quality control strategies ...

Element2 Group

QC Inspector

Southbridge, MA · On-site

$19 - $23.75/hr

The QC Inspector will be responsible for performing inspections throughout the manufacturing ... Perform first article inspections (FAI) in accordance with applicable requirements. * Read and ...

Rust-Oleum

Mgr/Quality Control

Attleboro, MA

Rust-Oleum Corporation is a worldwide leader in protective paints and coatings for both home and ... Analyze quality control test results and provide feedback and interpretation to production ...

New

Kop-Coat, Inc.

Mgr/Quality Control

Attleboro, MA · On-site

Rust-Oleum Corporation is a worldwide leader in protective paints and coatings for both home and ... Analyze quality control test results and provide feedback and interpretation to production ...

New

Element2 Group

QC Inspector

Southbridge, MA · On-site

$19 - $23.75/hr

The QC Inspector will be responsible for performing inspections throughout the manufacturing ... Perform first article inspections (FAI) in accordance with applicable requirements. * Read and ...

next page

Showing results 1-20

All JobsQuality Control In JobsQuality Control In Jobs in Sutton, MA

Quality Control In information

See Sutton, MA salary details

$31.9K

$85K

$135.4K

How much do quality control in jobs pay per year?

As of Aug 30, 2026, the average yearly pay for quality control in in Sutton, MA is $85,003.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,200.00 and $104,500.00 per year, depending on experience, location, and employer.

What is the difference between Quality Control In vs Quality Control Inspector?

AspectQuality Control InQuality Control Inspector
Primary RoleOversees quality assurance processes within production or manufacturing teams, ensuring compliance with standards.Performs inspections and tests on products or materials to identify defects or deviations from specifications.
CredentialsOften requires certifications like ISO or Six Sigma, with experience in quality management systems.Typically requires technical training or certifications such as ASQ Certified Quality Inspector.
Work EnvironmentWorks mainly in manufacturing or production settings, collaborating with quality teams and production staff.Works on the production floor or in labs, inspecting products directly.

While both roles focus on quality, Quality Control In involves managing quality processes and systems, whereas Quality Control Inspectors perform hands-on product inspections. Both roles are essential for maintaining product standards but differ in scope and responsibilities.

What does a quality control in job do?

A quality control in job involves inspecting products or services to ensure they meet specified standards and quality requirements. It includes tasks such as testing, measuring, and reviewing processes, often using tools like checklists or testing equipment, to identify defects and ensure customer satisfaction.

What cities near Sutton, MA are hiring for Quality Control In jobs?

Cities near Sutton, MA with the most Quality Control In job openings:

Quality Control In jobs near you
Infographic showing various Quality Control In job openings in Sutton, MA as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, 5% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $85,003 per year, or $40.9 per hour.

Vice President, Quality Control

Needham, MA • On-site

Candel Therapeutics
Biotechnology Research and Development • 51 - 200 employees
Learn more about Candel Therapeuticsexternal

$290K - $335K/yr

Full-time

Posted 14 days ago

Job description

Hybrid role: (2-3 days a week in Needham office)
Salary: $290K - $335K
Why Work With Us?
At Candel, our people drive our success. We value diversity, collaboration, and bold thinking in a supportive, mission-driven environment. Like a team, we show up for each other and stay focused on making a difference for patients and families. Our leadership is transparent and empowering, and our culture is built on trust, flexibility, and accountability, encouraging ownership and innovation every day.
Our Science: Advancing Cancer Immunotherapies
Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, it's an exciting time to join us and help bring transformative cancer treatments to patients. Learn more:www.candeltx.com
Position Summary
The Vice President, Quality Control will provide strategic, technical, and operational leadership for all Quality Control functions supporting the development, manufacture, release, and lifecycle management of viral vector and advanced therapy products. This role serves as a key member of the CMC and Quality leadership team, ensuring that QC strategy, laboratory operations, and data integrity systems align with regulatory requirements, product quality objectives, and commercial readiness. The VP, Quality Control will oversee testing strategies, specification setting, method qualification/validation, transfer, and lifecycle management of QC systems supporting both clinical and commercial programs.Key Interfaces
This role will work closely with CMC leadership, Analytical Development, Process Development, Manufacturing, Quality Assurance, Regulatory Affairs, Clinical Development, Supply Chain, Program Management, external laboratories (CROs/CDMOs), and executive leadership.Key Responsibilities
  • Establish and lead the global Quality Control strategy, including laboratory infrastructure, testing frameworks, and lifecycle management across development and commercial programs.
  • Provide governance and oversight for QC systems including specifications, test methods, environmental monitoring, stability programs, reference standards, and batch release support.
  • Ensure QC activities are compliant with global regulatory requirements (FDA, EMA, ICH) including cGMP expectations and data integrity standards.
  • Lead method qualification, validation, transfer, and performance monitoring in partnership with Analytical Development.
  • Oversee internal and external laboratory operations, including CROs and CDMOs.
  • Drive QC support for manufacturing operations including in-process, release, and stability testing.
  • Provide leadership for OOS/OOT investigations, deviations, and CAPA implementation.
  • Support regulatory submissions and inspections in collaboration with QA and Regulatory Affairs.
  • Advance QC through digital transformation, automation, and laboratory systems (LIMS, ELN).
  • Build and lead a high-performing QC organization.
  • Manage budgets, capital planning, and resources aligned to program priorities.
Required Qualifications
  • Advanced degree in a scientific discipline preferred or equivalent experience.
  • 15+ years of experience in Quality Control in the biopharmaceutical industry.
  • Experience supporting biologics, viral vector, or advanced therapy products.
  • Strong knowledge of QC systems including validation, microbiology, stability, and data integrity.
  • Experience with global regulatory submissions and inspections.
  • Proven leadership and team management capabilities.
Preferred Qualifications
  • Experience building or transforming QC organizations.
  • Experience with advanced therapy modalities (gene therapy, viral vectors).
  • Experience implementing digital QC systems.
  • Experience managing external laboratory networks.
  • Industry leadership through publications or regulatory engagement.
Leadership Competencies
  • Strategic leadership with strong quality and regulatory expertise.
  • Ability to influence cross-functional teams.
  • Strong risk-based decision making.
  • Commitment to quality culture and inspection readiness.
  • Excellent communication skills.

Must be authorized to work in US. We cannot provide sponsorships.
We are not open to agency resume submissions at this time

Apply