ZipRecruiter

Log In

1

Assistant Quality Control Manager Jobs in Edison, NJ

Tutor Perini

QC Field Engineer

New York, NY · On-site

$145K - $185K/yr

... * Assist with the creation of project specific Quality Management Plans and verify implementation of plan for each project * Assist with the development of Quality metrics that empower teams to ...

Tutorperini

QC Field Engineer

New York, NY · On-site

$145K - $185K/yr

... * Assist with the creation of project specific Quality Management Plans and verify implementation of plan for each project * Assist with the development of Quality metrics that empower teams to ...

CookUnity

Quality Control Supervisor

New York, NY

This role involves managing the QC team, planning audits, coordinating with cross-functional departments, and maintaining documentation that supports food safety, labeling accuracy, and efficient ...

CookUnity

Quality Control Supervisor

New York, NY · On-site

$22 - $25/hr

This role involves managing the QC team, planning audits, coordinating with cross-functional departments, and maintaining documentation that supports food safety, labeling accuracy, and efficient ...

CookUnity

Quality Control Supervisor

New York, NY · On-site

$22 - $25/hr

This role involves managing the QC team, planning audits, coordinating with cross-functional departments, and maintaining documentation that supports food safety, labeling accuracy, and efficient ...

Medline

Supv QC

Tinton Falls, NJ · On-site

$79K - $119K/yr

Job Summary Oversee and manage the Quality Control functions and personnel at designated distribution center. Responsibilities Include inspection, product disposition, holding and releasing of ...

Medline

Supv QC

Tinton Falls, NJ · On-site

$79K - $119K/yr

Job Summary Oversee and manage the Quality Control functions and personnel at designated distribution center. Responsibilities Include inspection, product disposition, holding and releasing of ...

Medline

Supv QC

Tinton Falls, NJ · On-site

$79K - $119K/yr

Job Summary Oversee and manage the Quality Control functions and personnel at designated distribution center. Responsibilities Include inspection, product disposition, holding and releasing of ...

Cellares

Quality Control Raw Material Analyst

Bridgewater, NJ · On-site

$24.50 - $33/hr

This is a hands-on, laboratory-facing role reporting to the Senior Manager, QC Raw Materials ... Support internal audits and external regulatory inspections; assist with preparation of audit-ready ...

Medline

Supv QC

Tinton Falls, NJ

$79K - $119K/yr

Job Summary Oversee and manage the Quality Control functions and personnel at designated distribution center. Responsibilities Include inspection, product disposition, holding and releasing of ...

Cellares

Quality Control Raw Material Analyst

Bridgewater, NJ · On-site

$24.50 - $33/hr

This is a hands-on, laboratory-facing role reporting to the Senior Manager, QC Raw Materials ... Support internal audits and external regulatory inspections; assist with preparation of audit-ready ...

Kommissary

Quality Control Technician

New York, NY · On-site

$20.50 - $26.25/hr

Essential Duties and Responsibilities The Quality Control Technician will perform routine quality ... management. * Provide real-time feedback to production staff to correct quality issues. * Assist ...

MW Industries

Quality Control Coordinator

Fairfield, NJ

$20.25 - $27.75/hr

Coordinate quality training sessions for employees throughout the company. * Assist in developing ... Support Quality Management System (QMS) initiatives related to AS9100 and ISO 9001 requirements

previous page

Showing results 41-60

All JobsQuality Control JobsAssistant Quality Control Manager JobsAssistant Quality Control Manager Jobs in Edison, NJ

Assistant Quality Control Manager information

See Edison, NJ salary details

$12

$23

$41

How much do assistant quality control manager jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for assistant quality control manager in Edison, NJ is $23.64, according to ZipRecruiter salary data. Most workers in this role earn between $16.92 and $23.89 per hour, depending on experience, location, and employer.

What does an assistant quality control manager do?

An Assistant Quality Control Manager supports the Quality Control Manager in overseeing product quality and ensuring that manufacturing processes comply with company standards and regulatory requirements. They supervise quality control staff, assist in developing and implementing testing procedures, and analyze data to identify areas for improvement. Their role is crucial for maintaining product consistency, safety, and customer satisfaction, while also working to resolve any issues that may arise during production.

What are the key skills and qualifications needed to thrive as an assistant quality control manager?

To thrive as an Assistant Quality Control Manager, you need a solid understanding of quality assurance processes, statistical analysis, and industry-specific regulations, usually supported by a relevant bachelor's degree. Familiarity with quality management systems (QMS), inspection tools, and certifications such as Six Sigma or ISO 9001 is often expected. Strong attention to detail, leadership, and effective communication skills help foster team collaboration and drive process improvements. These competencies ensure consistent product quality, compliance, and operational efficiency within the organization.

What are some common challenges faced by an assistant quality control manager, and how can they be addressed?

Assistant Quality Control Managers often encounter challenges such as maintaining consistent quality standards across multiple shifts, managing tight production schedules, and ensuring compliance with changing regulations. Effective communication with both production staff and senior management is crucial for promptly addressing quality issues. Staying proactive by implementing regular training sessions and fostering a culture of continuous improvement can help mitigate these challenges and ensure smooth operations within the quality control team.

What is the difference between Assistant Quality Control Manager vs Quality Control Technician?

AspectAssistant Quality Control ManagerQuality Control Technician
CredentialsTypically requires a bachelor's degree in quality assurance, engineering, or related field; certifications like ASQ CQE are commonUsually holds a high school diploma or associate degree; certifications like ASQ CQPA may be preferred
Work EnvironmentWorks in office and lab settings, overseeing quality processes and team coordinationPrimarily lab or production floor, performing testing and inspections
Employer & Industry UsageUsed in manufacturing, pharmaceuticals, and food industries for supervisory rolesCommon in manufacturing and production plants for technical testing roles

The Assistant Quality Control Manager focuses on supervising quality assurance processes and managing teams, requiring more advanced education and certifications. In contrast, the Quality Control Technician performs hands-on testing and inspections, often with less formal education. Both roles are essential in maintaining product quality but differ in responsibilities and level of oversight.

What cities near Edison, NJ are hiring for Assistant Quality Control Manager jobs?

Cities near Edison, NJ with the most Assistant Quality Control Manager job openings:

Assistant Quality Control Manager jobs near you
Infographic showing various Assistant Quality Control Manager job openings in Edison, NJ as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 15% Part Time, 3% Temporary, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $49,174 per year, or $23.6 per hour.

Manager, CQV Quality Control

WuXi Biologics

Cranbury, NJ • On-site

Full-time

Re-posted 27 days ago

Job description

Job Title - Manager - SR Manager, CQV Quality Control
Work Location - Cranbuy NJ
Job Summary
The Manager, CQV Quality Control is responsible for the strategic and operational leadership of QC CQV (Commissioning, Qualification, and Validation) activities in support of clinical and commercial biologics manufacturing. This role oversees laboratory systems, analytical instrumentation lifecycle management, computerized systems, and CQV compliance to ensure reliable, compliant, and efficient QC operations.
The position provides leadership and direction to the QC CQV team, ensuring execution of qualification, calibration, maintenance, and system validation activities in accordance with cGMP requirements. The Manager serves as a key partner to Quality Assurance, Manufacturing, Facilities & Engineering, IT, and client teams to support inspection readiness, continuous improvement, and high-quality delivery
Job Responsibilities:
  • Provide leadership and oversight for daily QC CQV operations to ensure compliance with cGMP, regulatory requirements, and internal procedures.
  • Accountable for instrument and system lifecycle management, including qualification, calibration, preventive maintenance, and periodic review.
  • Ensure the execution and review of calibration plans, preventive maintenance (PM), and periodic review (PRE) activities for QC instruments and equipment.
  • Oversee qualification of analytical instruments, equipment, and systems, ensuring documentation meets regulatory and internal quality standards.
  • Lead and oversee computerized system validation activities for QC systems and analytical instrument software (e.g., Empower, 32Karat, SoloVPE, EndoScan-V).
  • Ensure all systems are maintained in a validated state, including user access management, audit trail review, system configuration, and data integrity compliance.
  • Ensure compliance with data integrity principles (ALCOA+) and applicable regulations (e.g., 21 CFR Part 11, EU Annex 11).

People & Resource Management
  • Lead, supervise, and develop the QC CQV team, including performance management, coaching, and career development.
  • Ensure appropriate training, qualification, and competency of staff to support CQV and system management activities
  • Allocate resources and manage workload to ensure timely execution of CQV deliverables.
  • Foster a culture of quality, accountability, collaboration, and continuous improvement.

Laboratory Systems & Equipment Management
  • Oversee vendor coordination and service activities for instrument maintenance, calibration, and repair in collaboration with Facilities & Engineering (F&E).
  • Ensure effective lifecycle management of analytical instruments and laboratory systems, including installation, qualification, operation, and retirement.
  • Oversee system performance, reliability, and compliance through routine monitoring and periodic review processes.
  • Manage QC fixed assets in alignment with company financial and asset management policies, including asset tracking, capitalization support, lifecycle status, and decommissioning activities.
  • Ensure accurate documentation and control of QC assets within asset management systems, and support periodic asset verification, audits, and reconciliation activities.
  • Partner with Finance, Procurement, and Facilities to support asset acquisition, transfer, and disposal processes in compliance with company procedures.

Computerized Systems & Lab Admin Oversight
  • Provide oversight for QC computerized systems (e.g., LIMS, Empower, LES, CisPro systems), ensuring compliant design, implementation, validation, and routine operation.
  • Lead and support system enhancements, optimization initiatives, and cross-site alignment activities.
  • Ensure proper configuration, maintenance, and continuous improvement of QC systems to meet operational needs.
  • Oversee data integrity self-inspections and ensure timely resolution of identified gaps.
  • Coordinate with IT and validation teams on system qualification, upgrades, and issue resolution.

Quality Systems & Continuous Improvement
  • Lead and support QC system improvement initiatives, including integration of WuXi Business System (WBS) tools (e.g., GEMBA, Tier boards).
  • Drive continuous improvement initiatives to enhance efficiency, compliance, and right-first-time execution.
  • Monitor and ensure adherence to QC compliance metrics aligned with QA Quality Council and Quality Management Review requirements.
  • Support and review QC SOPs and procedural updates related to CQV and system management.

Audit & Inspection Readiness
  • Ensure QC CQV readiness for internal audits, client audits, and regulatory inspections.
  • Participate in inspections and audits as SME for CQV and computerized systems.
  • Support responses to audit observations, regulatory inquiries, and CAPA implementation.

Cross-Functional & Client Support
  • Serve as a key QC CQV representative in cross-functional teams including QA, Manufacturing, MSAT, IT, and Facilities.
  • Collaborate with stakeholders to ensure alignment on system qualification, maintenance, and compliance requirements.
  • Support client interactions related to CQV scope, including participation in discussions, audits, and technical clarifications as needed.

Additional Responsibilities
  • Perform other duties as assigned based on business needs and organizational priorities.

Qualifications
  • Bachelor's degree in Biology, Chemistry, Pharmaceutical Sciences, Engineering, or a related field with 9-11 years of experience
  • Master's degree with 7-9 years of experience
  • PhD with 4-6 years of relevant experience
  • Extensive experience in QC laboratories and cGMP environments
  • Strong knowledge of analytical instrument qualification, calibration, and maintenance (e.g., UPLC, HPLC, CE, icIEF)
  • Demonstrated experience with computerized systems and regulatory requirements (21 CFR Part 11, EU Annex 11)
  • Strong understanding of data integrity principles (ALCOA+)
  • Proven experience in deviation management, change control, and audit support

Preferred Capabilities
  • Demonstrated people leadership and team management experience in a QC or biopharmaceutical environment
  • Experience overseeing laboratory systems such as LIMS, Empower, LES, and inventory systems
  • Strong understanding of CQV lifecycle and computerized system validation
  • Experience driving continuous improvement and operational excellence initiatives
  • Ability to manage multiple priorities in a fast-paced, client-facing environment
  • Strong communication and stakeholder management skills

The anticipated salary range for this position is $73,000 - $150,000.
The job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs. An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation and gender.

Apply