Top 68 supplier quality engineer Jobs in new jersey

Quality Engineer
Interact Engineering LLC —Whippany, NJ
- $45 an hour
- Temporary
- 5 years
- Mid-level
- Master's degree
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Quality Packaging Engineer
Atrium —Holmdel, NJ
- $120,000 - $130,000 a year
- Mid-level
- 3 years
- Travel
- Paid time off
- Vision insurance
Quick Apply
Quality Associate -- Vendor Quality Management
Interact Engineering LLC —Whippany, NJ
- $50 an hour
- Temporary
- Mid-level
- Bachelor's degree
- Continuous improvement
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Quality Engineer
Fulfillment Recruiting —Kearny, NJ
- $80,000 - $100,000 a year
- Full-time
- 6 years
- 5 years
- Bachelor of Science
- Paid holidays
- Health insurance
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Specialist, Quality Engineer
L3 Harris —Camden, NJ
- $84,000 - $135,000 a year
- Full-time
- Mid-level
- Mentoring
- Associate's degree
- Paid holidays
- 401(k)
3d
QA Associate VQM
Synerfac Technical Staffing —Whippany, NJ
- $45 - $50 an hour
- Mid-level
- Bachelor's degree
- Continuous improvement
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Associate Director, Audit Strategy and Vendor Quality
BMS —Princeton, NJ
- $163,210 - $197,770 a year
- Email
- Hybrid work
- Bachelor of Science
- 8 years
- Analysis skills
- Paid holidays
- Disability insurance
2d
Quality Engineer I
Holtec —Camden, NJ
- $70,000 - $85,000 a year
- Mid-level
- High school diploma or GED
- Analysis skills
- Wellness program
- Commuter assistance
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Program Quality Engineering Manager
Lockheed Martin Corporation —Moorestown, NJ
- $122,900 - $216,660 a year
- Full-time
- 8 years
- Analysis skills
- Bachelor's degree
- Paid jury duty
- Paid holidays
QUALITY ENGINEER
Zenith LifeScience —South Plainfield, NJ
- $65,000 - $75,000 a year
- Full-time
- Mid-level
- Bachelor's degree
- Continuous improvement
Supplier Excellence Engineer
Kenvue —Summit, NJ
- $90,100 - $127,200 a year
- Hybrid work
- Analysis skills
- Travel
- Senior level
- Paid holidays
Product Quality Engineer
OrganOx —Madison, NJ
- $90,000 - $105,000 a year
- Full-time
- Microsoft Outlook
- Travel
- Organizational skills
- Paid holidays
- Disability insurance
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Quality Engineer III
Holtec —Camden, NJ
- $95,000 - $110,000 a year
- Hybrid work
- Management
- Construction site
- Engineering
- Wellness program
- Commuter assistance
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Quality Engineer
Cartridge Actuated Devices —Fairfield, NJ
- $90,000 - $115,000 a year
- Full-time
- CAD
- Mid-level
- Ability to lift 50 pounds
- Health savings account
- Health insurance
Quick Apply
ENGINEER, QUALITY (AIRCRAFT)
Valcor Engineering Corporation —Springfield, NJ
- $90,000 - $115,000 a year
- Full-time
- Mid-level
- Analysis skills
- Experience equivalent to degree accepted
- Health savings account
- Paid holidays
Quick Apply
Supplier Quality Engineer
Lockheed Martin Corporation —Moorestown, NJ
- $67,000 - $117,990 a year
- Full-time
- Mid-level
- Analysis skills
- Travel
- Paid jury duty
- Paid holidays
7d
Supplier Quality Associate Manager
Lockheed Martin Corporation —Moorestown, NJ
- $99,700 - $175,835 a year
- Full-time
- Microsoft Excel
- Mid-level
- Presentation skills
- Paid jury duty
- Paid holidays
7d
Quality Auditor - Pharma/Food/Med Device
SQA Services —Newark, NJ
- $1,300 a day
- Contract
- 5 years
- Writing skills
- Residential
Quick Apply
CQV Engineer II
IPS-Integrated Project Services —Somerset, NJ
- $79,750 - $106,300 a year
- Full-time
- Construction site
- Ability to walk for extended periods
- Bachelor of Science
- Paid holidays
- Disability insurance
4d
Quality Engineer
Recruits Lab —Phillipsburg, NJ
- $36.06 - $43.27 an hour
- Contract
- 5 years
- Analysis skills
- Bachelor's degree
Quick Apply

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supplier quality engineer jobs near new jersey

Quality Engineer

Interact Engineering LLC
Whippany, NJ

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Job Details

Temporary | Full-time
$45 an hour

Qualifications

Chemical Engineering
Drug regulation
Master's degree
Manufacturing facility
Bachelor's degree
Medical device manufacturing facility experience
Pharmaceutical company experience
Cleanroom
Biomedical regulatory compliance
Root cause analysis
ISO 13485
FDA regulations
Pharmaceutical manufacturing facility experience

Full Job Description

OVERVIEW

The Quality Engineer will support the aseptic manufacturing and quality systems for sterile drug products packaged in glass vials and prefilled syringes. This role ensures compliance with applicable regulatory requirements including US FDA 21 CFR Parts 210, 211, 820, EU GMP Annex 1, and ISO 13485.

The position is responsible for the Quality support functions associated with the manufacturing and packaging of aseptic fill products like Syringes, vials and Cartridges. The position is responsible for the timely assessment of Quality documents associated with the production and packaging of aseptic fill products. This position will also manage projects associated with process, documentation and other improvements necessary in the Quality arena.

This role is 100% on site in Whippany, NJ.

ESSENTIAL FUNCTIONS

Key Responsibilities:

1. Quality Systems & Compliance

o Ensure compliance with cGMP, Quality System Regulations (QSR), and ISO 13485 requirements in aseptic manufacturing and packaging.

o Support the implementation and continuous improvement of quality systems: CAPA, deviations, change control, risk management, and supplier qualification.

o Author, review, and approve SOPs, protocols, batch records, and validation documents.

o Maintain compliance with FDA 21 CFR Part 210/211 (drug manufacturing), Part 820 (device QSR), and EU Annex 1 sterile manufacturing requirements.

2. Aseptic Manufacturing Oversight

o Provide on-floor quality support for aseptic filling operations of glass vials and prefilled syringes.

o Perform aseptic technique observation, media fill support, and personnel qualification oversight.

o Review and assess cleanroom classification, environmental monitoring, and process simulations.

o Verify compliance of gowning, cleaning, and disinfection practices per EU Annex 1 and FDA expectations.

3. Process & Equipment Support

o Support validation and qualification of aseptic filling lines, isolators, RABS, cleanrooms, utilities, and associated equipment.

o Participate in FAT, SAT, IQ/OQ/PQ and technical transfers for sterile manufacturing lines.

o Ensure equipment, packaging, and container-closure systems for glass vials and prefilled syringes meet USP <1207> container closure integrity testing (CCIT) requirements.

o Conduct risk assessments (FMEA, HACCP, risk-based approach per ICH Q9/Q10).

4. Investigations & Continuous Improvement

o Lead and support root cause investigations for deviations, OOS/OOT, and complaints related to aseptic operations and packaging.

o Develop and track CAPAs to ensure timely and effective implementation.

o Monitor process performance and quality trends to identify opportunities for improvement.

o Drive implementation of quality by design (QbD) and continuous improvement initiatives in aseptic processes.

5. Documentation & Regulatory Support

o Ensure accurate, complete, and contemporaneous documentation in compliance with data integrity principles (ALCOA+).

o Support preparation for regulatory inspections (FDA, EMA, Notified Body, MHRA, etc.).

o Assist in responding to inspection findings and regulatory queries.

o Prepare quality reports, metrics, and risk assessments for management review.

6. Continuous Improvement:

o Drive continuous improvement initiatives through lean manufacturing principles and Six Sigma methodologies.

o Lead quality improvement projects, collaborating with teams to enhance product quality, reduce waste, and improve operational efficiency.

POSITION QUALIFICATIONS

EDUCATION/EXPERIENCE:

· Bachelor’s or master’s degree in pharmacy, Microbiology, Biotechnology, Chemical Engineering, or related Life Sciences/Engineering field.

· 5+ years of experience in aseptic pharmaceutical or medical device manufacturing, with direct involvement in glass vial and/or prefilled syringe filling operations.

· Strong understanding of cGMP, FDA 21 CFR Parts 210/211/820, EU Annex 1, ISO 13485.

· Experience with validation, aseptic process simulations, cleanroom classification, and CCIT.

· Prior exposure to combination product regulations is highly desirable.

Skills & Competencies:

o Strong knowledge of aseptic techniques, sterile barrier systems, and contamination control strategies.

o Familiarity with quality risk management, statistical data analysis, and process capability tools.

o Excellent technical writing and communication skills.

o Strong problem-solving and root cause analysis skills.

o Ability to work in a dynamic, fast paced, and highly regulated environment.

Physical Requirements:

o Primarily site-based with routine presence in classified cleanroom environments.

o Ability to stand for up to 8 hours per day.

Frequent sitting, standing, walking, reading written documents and use of computer monitor screen, talking, writing, listening

o May require gowning certification for Grade A/B aseptic areas.

o Occasional travel for supplier audits, training, or regulatory inspections.

Pay: $45.00 per hour

Work Location: In person

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Refine Your Search

supplier quality engineer jobs in new jersey

Quality Engineer

Quality Packaging Engineer

Quality Associate -- Vendor Quality Management

Quality Engineer

Specialist, Quality Engineer

QA Associate VQM

Associate Director, Audit Strategy and Vendor Quality

Quality Engineer I

Program Quality Engineering Manager

QUALITY ENGINEER

Supplier Excellence Engineer

Product Quality Engineer

Quality Engineer III

Quality Engineer

ENGINEER, QUALITY (AIRCRAFT)

Supplier Quality Engineer

Supplier Quality Associate Manager

Quality Auditor - Pharma/Food/Med Device

CQV Engineer II

Quality Engineer

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