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Vice President Cement Quality Control Jobs (NOW HIRING)

Titan America

Senior Quality Control Manager

Medley, FL · On-site

$110 - $140/hr

Our products include cement, aggregate, ready-mixed concrete, and fly ash beneficiation. TITAN ... Titan Florida LLC seeks a Quality Control Manager to work at the Pennsuco Complex located in Medley ...

Titan America

Senior Quality Control Manager

Medley, FL · On-site

Our products include cement, aggregate, ready-mixed concrete, and fly ash beneficiation. TITAN ... Titan Florida LLC seeks a Quality Control Manager to work at the Pennsuco Complex located in Medley ...

Cement Recruiter

Quality Supervisor

Pryor, OK

Direct the activities of the Quality Control Laboratory, which includes training and supervising ... Work with customers to resolve any issues/complaints regarding the cement quality or delivery of ...

Titan America

QC Lab Supervisor

Medley, FL · On-site

Our products include cement, aggregate, ready-mixed concrete, and fly ash beneficiation. TITAN ... Titan Florida, LLC, has an opening for a Quality Control Lab Supervisor in the Cement Division.

Titan America

QC Lab Supervisor

Medley, FL

Our products include cement, aggregate, ready-mixed concrete, and fly ash beneficiation. TITAN ... Titan Florida, LLC, has an opening for a Quality Control Lab Supervisor in the Cement Division.

Titan America

QC Lab Supervisor

Medley, FL

Our products include cement, aggregate, ready-mixed concrete, and fly ash beneficiation. TITAN ... Titan Florida, LLC, has an opening for a Quality Control Lab Supervisor in the Cement Division.

Titan America

QC Lab Supervisor

Medley, FL

Our products include cement, aggregate, ready-mixed concrete, and fly ash beneficiation. TITAN ... Titan Florida, LLC, has an opening for a Quality Control Lab Supervisor in the Cement Division.

Gray Construction

Vice President, Quality

Lexington, KY · On-site

$180 - $280/hr

The Vice President, Quality leads and advances Gray's national construction quality program, overseeing field quality assurance and control, root cause analysis, corrective actions, and the ...

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Vice President Cement Quality Control information

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$31K

$125.6K

$213.5K

How much do vice president cement quality control jobs pay per year?

As of Aug 31, 2026, the average yearly pay for vice president cement quality control in the United States is $125,600.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,000.00 and $151,000.00 per year, depending on experience, location, and employer.

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Vice President Cement Quality Control jobs near you

Vice President, Quality Control

Needham, MA • On-site

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

Full-time

Posted 13 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 InterfacesThis 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

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