Top 61 Chemical engineer Jobs in New York, Ny

Quality Engineer
Interact Engineering LLC —Whippany, NJ
- $45 an hour
- Temporary
- 5 years
- Mid-level
- Master's degree
Quick Apply
Manufacturing Engineer
Fortira Inc —Pearl River, NY
- $28 - $32 an hour
- Weekends as needed
- Bachelor's degree
- In-person
- Communication skills
Quick Apply
5d
Product Development Engineer (Chemical)
KLA —Totowa, NJ
- $106,000 - $180,200 a year
- Full-time
- Doctoral degree
- Master's degree
- Analysis skills
- Employee stock purchase plan
- Paid holidays
6d
Assistant Engineer (Environmental) / Engineer Trainee - NY HELPS
State of New York - Environmental Conservation, Department of —Long Island City, NY
- $70,951 - $111,621 a year
- Overtime
- Background check
- Construction site
- Driver's License
- Paid holidays
- Dental insurance
Quality Chemical Engineer
KLA —Totowa, NJ
- $60,400 - $102,700 a year
- Part-time
- Mid-level
- Bachelor's degree
- Travel
- Employee stock purchase plan
- Paid holidays
Chemical Product Engineer ( Process|Tool)
KLA —Totowa, NJ
- $85,600 - $145,500 a year
- Full-time
- Mid-level
- Master's degree
- Bachelor's degree
- Employee stock purchase plan
- Paid holidays
Area Engineer
Agency DEPT OF ENVIRONMENT PROTECTION —New York, NY
- $62,407 - $169,806 a year
- Full-time
- Civil engineering
- 6 years
- Mid-level
- Loan forgiveness
Biologics Process Development Scientific Lead
Merck —Rahway, NJ
- $210,400 - $331,100 a year
- Full-time
- Bachelor of Science
- 11+ years
- Bachelor's degree
- Paid holidays
- Health insurance
Senior Medical Device Research and Development Engineer
Cresilon, Inc. —Brooklyn, NY
- $60,000 - $160,000 a year
- Full-time
- Microsoft Word
- Anatomy knowledge
- 5 years
- Paid holidays
- Disability insurance
Quick Apply
Product Development Engineer (Analytical Hardware)
KLA —Totowa, NJ
- $85,600 - $145,500 a year
- Full-time
- Master's degree
- Analysis skills
- Bachelor's degree
- Employee stock purchase plan
- Paid holidays
Senior Scientist, Engineering, Crystallization Lab (Onsite)
Merck —Rahway, NJ
- $117,000 - $184,200 a year
- Full-time
- 5 years
- Bachelor of Science
- Analysis skills
- Paid holidays
- Health insurance
Research Scholar (Part-time)
New York University —Brooklyn, NY
- $26.37 an hour
- Part-time
- Bachelor of Science
- Mid-level
- University
Associate Principal Scientist, Downstream Process Development
Merck —Rahway, NJ
- $142,400 - $224,100 a year
- Full-time
- Bachelor of Science
- 3 years
- Master's degree
- Paid holidays
- Health insurance
13d
Process Improvement Engineer II (NYC)
Victoria's Secret —New York, NY
- $88,200 - $117,285 a year
- Full-time
- Mid-level
- Travel
- Organizational skills
Post Doctoral Associate Positions
New York University —Brooklyn, NY
- $90,000 a year
- University
- Doctor of Philosophy
- US work authorization
BOB-Administrative Engineer (NM)
Agency DEPARTMENT OF TRANSPORTATION —New York, NY
- $62,407 - $169,806 a year
- Weekends as needed
- Management
- Mid-level
- Master's degree
- Loan forgiveness
Associate Principal Scientist Engineer, Drug and Device Combination Products (Onsite)
Merck —Rahway, NJ
- $142,400 - $224,100 a year
- Full-time
- 7 years
- Master's degree
- Doctor of Philosophy
- Paid holidays
- Health insurance
Wastewater Process Engineer
CREW Carbon —Brooklyn, NY
- $85,000 - $130,000 a year
- Full-time
- 5 years
- Office
- Master's degree
- Health insurance
- 401(k)
Quick Apply
5d
Lead Value Engineer - Energy
Celonis —New York, NY
- $157,000 - $212,000 a year
- Full-time
- Hybrid work
- 7 years
- Oracle
- Computer Science
- Paid time off
- Parental leave
Post Doctoral Associate
New York University —Brooklyn, NY
- $78,000 - $85,000 a year
- University
- Doctor of Philosophy
- US work authorization

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chemical engineer jobs near new york, ny

Quality Engineer

Interact Engineering LLC
Whippany, NJ

Quick Apply

Job Details

Temporary | Full-time
$45 an hour

Qualifications

Chemical Engineering
Drug regulation
Master's degree
Manufacturing facility experience
Bachelor's degree
Medical device manufacturing facility experience
Pharmaceutical company experience
Cleanroom experience
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

Quick Apply

Refine Your Search

chemical engineer jobs in new york, ny

Quality Engineer

Manufacturing Engineer

Product Development Engineer (Chemical)

Assistant Engineer (Environmental) / Engineer Trainee - NY HELPS

Quality Chemical Engineer

Chemical Product Engineer ( Process|Tool)

Area Engineer

Biologics Process Development Scientific Lead

Senior Medical Device Research and Development Engineer

Product Development Engineer (Analytical Hardware)

Senior Scientist, Engineering, Crystallization Lab (Onsite)

Research Scholar (Part-time)

Associate Principal Scientist, Downstream Process Development

Process Improvement Engineer II (NYC)

Post Doctoral Associate Positions

BOB-Administrative Engineer (NM)

Associate Principal Scientist Engineer, Drug and Device Combination Products (Onsite)

Wastewater Process Engineer

Lead Value Engineer - Energy

Post Doctoral Associate

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