Quality Assurance Lead Jobs in New Jersey
Quality Assurance Lead jobs in New Jersey are consistently in demand, concentrated in pharmaceuticals and life sciences, medical devices, and consumer packaged goods, with openings at every level from entry-level QA specialist to senior lead. The heaviest hiring is in and around Newark, Parsippany, and Princeton, where companies like Johnson and Johnson, Becton Dickinson, and Merck maintain major operations. The most sought-after specialties include GMP compliance, regulatory affairs quality, and software or systems quality assurance. Find a role that fits below and apply directly.
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CooperSurgical is a leading fertility and women’s healthcare company dedicated to putting time on the side of women, babies, and families at the healthcare moments that matter most in life. As a division of CooperCompanies, we're driven by a unified purpose to enable patients to experience life's beautiful moments. Guided by our shared values – dedicated, innovative, friendly, partners, and do the right thing – our offerings support patients throughout their lifetimes, from contraception to fertility and birth solutions, to women’s and family care, and beyond. We currently offer over 600 clinically relevant medical devices to healthcare providers, including testing and treatment options, as well as an innovative suite of assisted reproductive technology and genomic testing solutions. Learn more at www.coopersurgical.com.
The Life Science Quality Assurance Specialist III is a senior-level employee who reports to the Life Science Quality Manager. Will own Quality Systems working with stakeholders in facilitating meetings, providing data from tracking and trending, leading quality and continuous improvements. Role will have the responsibility to train the organization on the Quality Systems, as well as mentoring Quality Team members. Will help drive change that will remediate the risks to internal and external customers. Primarily responsible for establishing, developing, implementing, maintaining and improving Quality System processes and programs to include Quality Event Reporting (Deviations, Nonconformance, Change Management, CAPA, Complaint), Document Control Program, Supplier Qualification, Validations, and Product Transfer. In this role the candidate will mentor and train new personnel on the Quality System(s). Will partner with stakeholders to improve the quality program and culture.
- Understands and applies comprehensive knowledge of quality principles and maintains current understanding of regulations.
- Familiarity or experience with the following is strongly preferred: Basic statistics, review/approval of documentation; risk tools, technical writing, and writing/reviewing/approving investigations.
- Knowledge of Master Control, or similar eQMS a plus
- Demonstrated experience and proficiency in Microsoft Office applications, Word, Excel and PowerPoint.
- Responds effectively to changing constraints.
- Good interpersonal skills and ability to work effectively and efficiently in a team environment to accomplish goals.
- Understands the drivers of change and anticipates the implications of changing political and practical circumstances
- Applies a preventative instead of corrective approach Attention to Detail
- Checks information, picks up inconsistencies and mistakes and can make detailed comparisons between similar sources
- Positive work attitude that supports teamwork and continuous improvement.
- Makes pragmatic decisions based on range of factors
- Able to make decisions quickly where necessary, based on incomplete information
- Demonstrates logic to back up decisions
- Excellent critical analytical skills – ability to find root cause of why and issue occurred.
- Identifies ways to improve processes/situations
- Takes responsibility for improvements or solving problems.
- Must display eagerness to learn and continuously improve.
- Sets own standards above prevailing standards, shows dissatisfaction with substandard or inefficient activities Interpersonal Skills
- Socially capable - interacts confidently, reads the situation
- Empathetic and can evaluate likely reactions
- Collaborative approach
- Ability to focus on important issues only. Risk based approach
- Regularly refocuses on results
- Demonstrates a drive to exceed performance targets
- Ability to handle multiple tasks and competing priorities concurrently and in a timely fashion
- Prioritizes and monitors tasks progress
- Makes realistic estimates of time and resource requirements
- The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- While performing the duties of this job, the employee is regularly required to sit and talk or hear. The employee is occasionally required to stand; walk; use hands to finger, handle, or feel; and reach with hands and arms. Specific vision abilities required by this job include close vision.
- Bachelor’s degree (BA/BS ) from four-year college or university or associate degree (A.A.) with four to six years related experience and/or training.
- OR six to eight years related experience and/or training.
- OR equivalent combination of education and experience
Experience
- Candidates must show knowledge and proficiency in the Quality Assurance Specialist II role
- Candidate should demonstrate knowledge of regulations and standards such as:
AABB, AATB, FDA (HCT/P, cGMP, cGTP), 21CFR1271, FACT and ISO 9001 regulations
- Maintains a culture of quality awareness, teamwork, and cooperation with Quality customers.
- Provide Quality oversight, support and engagement as needed by Operations.
- Owner of Quality Management System Processes such as:
- Document Control Program: review, approval, and maintenance of company Standard Operating Procedure via electronic Document Quality Management System. Ensuring stakeholders are adhering to company policies and templates.
- Change Management Program: Review, approve and track changes to approved procedures, validated software and processes, qualified equipment. Review the change task completion. Track and facilitate investigation in cross functional impacted teal to support closure of Change Control.
- Deviations and Nonconformances: Review, approve and monitor the events and deviations. Complaint handling and investigations Track and facilitate investigation in cross functional team discussions in support of closing Quality Events
- Supply/ Vendor Management: Supplier qualification, reassessment activities, quality agreements, quality score cards. Oversee the process is maintained and approved according to processes.
- Validations: Review and approval of equipment, systems validation/ qualification, and any design transfer to operations
- Quality Metrics: Perform trending analysis and reporting of quality indicators. Identification or risk and process improvements into operations.
- Facilitate meetings, provide system visibility, communicate status, and facilitate closure of aging items.
- Gather performance metrics and coordinate Management review inputs from various contributing departments.
- Track, trend, and report Quality System metrics to ensure continuous quality improvements while communicating critical compliance and quality risks.
- Work cooperatively in a team environment to maintain cross functional, and cross site processes and procedural consistency for quality systems records.
- Create and implement a training program for the QMS processes to educate Quality Assurance customers.
Perform other Quality Assurance Duties as required.
See All 80 Quality Assurance Lead Jobs in New Jersey
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Find Quality Assurance Lead JobsQuality Assurance Lead Jobs by City in New Jersey
Where New Jersey roles are concentrated, by current openings.
Quality Assurance Lead Job Market in New Jersey
A snapshot from current New Jersey openings, updated as new roles post.
Who's Hiring


Top Industries Hiring
- Biotechnology & Pharmaceuticals
- Medical Devices
- Technology & Software
- Consulting & Professional Services
- Retail
What New Jersey Employers Look For
The qualifications that appear most often in quality assurance lead jobs across New Jersey.
- Bachelor's degree in life sciences, engineering, or a related field required
- Demonstrated experience with GMP, ISO 9001, or FDA regulatory compliance frameworks
- Proven ability to lead root cause analysis and corrective action processes
- Hands-on experience with quality management systems such as Veeva or MasterControl
- Strong familiarity with New Jersey pharmaceutical or medical device manufacturing environments
- ASQ Certified Quality Auditor or Certified Quality Engineer credential preferred by employers
Quality Assurance Lead Jobs in New Jersey: Frequently Asked Questions
How do you become a quality assurance lead in New Jersey?
Most quality assurance lead roles in New Jersey require a bachelor's degree in a life sciences, engineering, or technical discipline, since no state-issued license is required for the role itself. Employers in the pharmaceutical and medical device sectors, which dominate New Jersey hiring, strongly prefer candidates with hands-on GMP or FDA-regulated environment experience. Earning an ASQ credential such as the Certified Quality Engineer or Certified Quality Auditor meaningfully strengthens a candidacy in this market.
How much do quality assurance leads make in New Jersey?
Quality assurance leads in New Jersey earn a median of about $119,470 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $70,150 for the lowest 10% to over $168,680 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire quality assurance leads in New Jersey?
Employers hiring quality assurance leads in New Jersey right now include Integra LifeSciences, SGS, and MIAX, based on current listings on Migrate Mate as of August 2026. New Jersey's deep concentration of pharmaceutical, biotechnology, and medical device headquarters makes it one of the most active states in the country for quality assurance hiring at the lead level.
Which New Jersey cities have the most quality assurance lead jobs?
The cities with the most quality assurance lead openings in New Jersey are Princeton, New Jersey, and Clifton. This distribution reflects the corridor of pharmaceutical and life sciences headquarters and manufacturing sites running through central and northern New Jersey, with suburban corporate campuses in areas like Parsippany and Princeton driving significant volume outside the major cities.
Are there remote quality assurance lead jobs in New Jersey?
Yes, but they are less common than in purely analytical fields, since many quality assurance lead roles require on-site presence for audits, lab oversight, or manufacturing floor activities. About 43% of quality assurance lead openings tied to New Jersey are remote or hybrid as of August 2026. The portions of the role most amenable to remote work include documentation review, supplier quality management, and regulatory submissions support.
How can I get hired as a quality assurance lead in New Jersey with little or no experience?
The most realistic entry path is starting as a quality assurance associate or QA specialist at one of New Jersey's pharmaceutical or medical device companies, then building toward a lead role through demonstrated ownership of investigations and audits. Large employers in the state regularly hire recent graduates with life sciences degrees into rotational quality programs or associate-level roles that develop the skills needed for a lead position. Earning an entry-level ASQ certification and gaining familiarity with a quality management system like Veeva gives candidates a concrete edge when competing for those openings.
Where can I find and apply to quality assurance lead jobs in New Jersey?
You can find and apply to quality assurance lead jobs in New Jersey on Migrate Mate, which lists current openings from employers hiring in the state right now. Search the listings to find roles that match your experience and specialization, and apply directly to the ones that fit.
See All 80 Quality Assurance Lead Jobs in New Jersey
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