Job Market Guide: Quality Assurance Manager jobs in NJ

Competition
Desired Skills
Years of Experience
Years of Experience distribution graph for Quality Assurance Managers in NJ. Quality Assurance Managers in NJ have between ${} and ${} years of experience, averaging $${} years of experience.

30 Quality Assurance Manager jobs in NJ

Ridgefield, NJ
In this role, you will be responsible for technical management of personnel involved in the development, transfer, and troubleshooting of routine and complex techniques associated with daily QC release.
industry
Biotech/Pharma
experience
5 - 7 years

QA Programs Mgr

Hancocks Bridge, NJ
In this role, you will participate as a key manager, providing input and monitoring of Business Planning, Budget, and Business Performance of the Nuclear Oversight (NOS) Department.
industry
Energy / Utilities
experience
11 - 15 years

Manager QA GCP

Edison, NJ
In this role, you will perform and manages all types of audits in the clinical studies audit program. It also includes the auditing schedule of clinical investigator sites (phases I to IV), GCP internal systems.
industry
Biotech/Pharma
experience
5 - 7 years

QA Manager

Jersey City, NJ
In this role, you will maintain product quality by enforcing QA policies and procedures and organizational requirements.
industry
Business Services
experience
8 - 10 years

$100K - $140K - Bedminster, NJ
In this role, the selected candidate will be responsible for the oversight and the conduct of audits as they relate to Good Clinical Practices (GCP), to ensure compliance with all established regulatory guidelines as well as company policies and procedures.
industry
Biotech/Pharma
experience
5 - 7 years

$60K - $90K - Union, NJ
As Manager of Quality Assurance, you will be responsible for the management of the quality assurance system, quality KPIs, overseeing the CAPA process, and qualifying vendors.
industry
Manufacturing / Packaging
experience
5 - 7 years

$100K - $140K - Hampton, NJ
In this role, the selected candidate will be responsible for the oversight and the conduct of audits as they relate to Good Clinical Practices (GCP), to ensure compliance with all established regulatory guidelines as well as company policies and procedures.
industry
Biotech/Pharma
experience
5 - 7 years

QA Manager

Princeton, NJ
In this role, the selected candidate will work closely with the QA and Development teams in understanding testing needs and priorities, and working with the automation team prioritize and deliver on projects that are defined.
industry
Diversified Industrial
experience
5 - 7 years

Hoboken, NJ
In this role, you will supports Release Management by contributing to and reviewing release approach.
industry
e-Commerce
experience
11 - 15 years

Parsippany, NJ
In this role, the candidate will conduct first party audits; reviews and appraisals for EM's and certain suppliers in accordance with Pinnacle Foods policy and procedures.
industry
IT Consulting/Services
experience
11 - 15 years

Senior IT QA Manager

Piscataway, NJ
In this role, the selected candidate will be responsible for devising and executing testing strategies that increases the use of test automation to improve testing speed and coverage.
industry
Business Services
experience
8 - 10 years

Trenton, NJ
The individual in this role works jointly with the Supply organization to provide for a timely and reliable supply of quality products.
industry
Biotech/Pharma
experience
8 - 10 years

Newark, NJ
In this role, the selected candidate will assist GCP and/or GLP inspections at internal and external locations.
industry
Biotech/Pharma
experience
5 - 7 years

Summit, NJ
In this role, the selected candidate will assist with development of global GMP policies, standards and procedures for data governance and data integrity in compliance with current and HealthCare Client Authority requirements and industry best practices.
industry
Biotech/Pharma
experience
5 - 7 years

Bridgewater, NJ
In this role, the selected candidate will review and approve raw materials and components, manufacturing documents, including standard formula, test analyses, batch production records and batch packaging records for release.
industry
Manufacturing / Diversified
experience
5 - 7 years

Franklin, NJ
In this role, the selected candidate must have an extensive experience with Sim Corp testing; manage testing activities across different department during Murex & SimCorp Integration.
industry
IT Consulting/Services
experience
15+ years

Manager, QA IMP - GMP

Edison, NJ
In this role, you will manage and lead the IMP release program and assures all suppliers and testing laboratories provide GMP compliant product release documentation. Participates as a cross-functional team member to provide product quality/GMP support and assures proper documentation of drug product release programs.
industry
Biotech/Pharma
experience
5 - 7 years

Fort Lee, NJ
In this role, the selected candidate will coordinate release content and effort based on the service request backlog. Planning the testing effort and providing estimates for new features and releases.
industry
Staffing & Recruiting
experience
5 - 7 years

Jersey City, NJ
As a QA team manager in our Global Technology organization, this individual will oversee all testing staff and activities for all assigned applications. Ensures all testing standards are being met.
industry
Financial Services
experience
5 - 7 years

Sr Manager, QA

Plainsboro, NJ
The Sr./Director Quality Assurance Manager, External Manufacturing manages and oversees the activities of external manufacturers to ensure products meet current Good Manufacturing Practices and Good Tissue Practices, applicable medical device regulatory requirements, and corporate quality and regulatory standards through interaction with business partners.
industry
Business Services
experience
11 - 15 years

$80K - $90K - Rutherford, NJ
In this role, the Quality Assurance Manager will provide exposure to both clinical- (CAP, CLIA) and biopharma (GCP)-regulated environments.
industry
Staffing & Recruiting
experience
5 - 7 years

Summit, NJ
In this position, you will conduct batch record review of development batches of drug substance, drug product and package/labeling jobs with particular emphasis on experience with reviewing Biologics including Cell Drug Batch Records.
industry
Biotech/Pharma
experience
Less than 5 years

Cape May, NJ
The QC Manager plans, directs and coordinates all on-site Quality Control (QC) activities to ensure compliance with applicable company, owner, and government regulations and requirements.
industry
Construction
experience
8 - 10 years

QA Programs Mgr

Hancocks Bridge, NJ
In this role, you will be responsible for developing, maintaining, and implementing the quality assurance program manual for the Salem and Hope Creek nuclear generating stations in accordance with federal regulations and the licensing basis commitments to quality assurance standards.
industry
Audio / Video
experience
11 - 15 years