Top 119 Production associate Jobs in Dunellen Nj

Operations Associate
Legend Biotech US —Raritan, NJ
- $59,168 - $77,658 a year
- Full-time
- Basic math
- Mid-level
- High school diploma or GED
Manufacturing Upstream Associate I/II
Kashiv BioSciences, LLC —Piscataway, NJ
- $30 - $38 an hour
- Overtime
- Microsoft Word
- High school diploma or GED
- Ability to lift 50 pounds
- Travel reimbursement
- Health savings account
Robotics Warehouse Associate
Amazon Warehouse —Edison, NJ
- $22.50 an hour
- Overtime
- 18 years or older
- Military encouraged
- Entry level
- Flextime
- On-the-job training
Production Associate - Builder/Material Handler
Cintas —Piscataway, NJ
- $19.25 - $24.08 an hour
- Full-time
- Background check
- 18 years or older
- Pass drug screening
- Profit sharing
- AD&D insurance
Picker (Warehouse Associate)
NetCost Market —South Plainfield, NJ
- $21 - $23 an hour
- Overtime
- Ability to walk for extended periods
- Forklift
- Warehouse experience
Quick Apply
Manufacturing Downstream Associate I/II
Kashiv BioSciences, LLC —Piscataway, NJ
- $30 - $38 an hour
- Overtime
- Microsoft Word
- Mid-level
- High school diploma or GED
- Travel reimbursement
- Health savings account
Production Associate
NIXON MEDICAL —Edison, NJ
- $18.50 an hour
- Full-time
- Ability to lift 50 pounds
- Ability to stand for extended periods
- Entry level
- Paid holidays
- Health insurance
Quick Apply
2d
IPQA Associate I
Ohm Laboratories Inc , USA —New Brunswick, NJ
- $30 - $37 an hour
- Monday to Friday
- Microsoft Excel
- Microsoft Outlook
- English
- Disability insurance
- Health insurance
Packaging Associate I
TailoredSearch —Plainfield, NJ
- $17.50 - $18.50 an hour
- Overtime
- High school diploma or GED
- Ability to lift 50 pounds
- 21 years or older
Quick Apply
12d
Quality Assurance Associate
Princeton BioMeditech Corporation —Middlesex County, NJ
- Mid-level
Post Harvest Associate
The QCC Group, LLC —Plainfield, NJ
- $17.50 an hour
- Weekends as needed
- Heavy lifting
- English
- US work authorization
- Health insurance
- Dental insurance
Quick Apply
Quality Control (QC) / Production Associate I (Chemist)
SOFIE —Somerset, NJ
- $24 - $28 an hour
- Weekends as needed
- Engineering
- High school diploma or GED
- Ability to lift 50 pounds
12d
Associate, Manufacturing (Helper)
US Pharma Lab —North Brunswick, NJ
- Extended hours
- No experience needed
- English
- High school diploma or GED
Production Associate
BERJE INCORPORATED —Carteret, NJ
- $22 - $24 an hour
- Ability to walk for extended periods
- High school diploma or GED
- Ability to lift 50 pounds
- Disability insurance
- Health insurance
Quick Apply
Quality Control Associate
Driscoll Foods —Wayne, NJ
- From $18 an hour
- Full-time
- Mid-level
- Ability to lift 50 pounds
- US work authorization
- Health insurance
- Dental insurance
Quick Apply
Associate Scientist, MSAT (Cell & Gene Therapy)
Legend Biotech US —Somerset, NJ
- $83,711 - $104,637 a year
- Full-time
- Mid-level
- Master's degree
- Bachelor's degree
Compliance Associate II
Ohm Laboratories Inc , USA —New Brunswick, NJ
- $74,000 - $82,500 a year
- Microsoft Excel
- Microsoft Outlook
- English
- Disability insurance
- Health insurance
Temp Conversion - Warehouse Associate - SUN-WED - 7:00 PM - 5:30 AM OB
ID Logistics —Somerset, NJ
- $19.50 an hour
- Temporary
- English
- Ob/Gyn
- Warehouse
- Disability insurance
- Health insurance
Associate Supervisor, Quality
Menasha Corporation & Companies —Edison, NJ
- $66,000 - $74,000 a year
- Full-time
- Microsoft Word
- Spanish
- Ability to walk for extended periods
- AD&D insurance
- Paid holidays
10d
Production Associate – 2nd Shift
Cytosorbents Medical Inc —Princeton, NJ
- $26 - $28 an hour
- Full-time
- Background check
- Basic math
- Mid-level
- Health insurance
- Paid time off
Quick Apply

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Operations Associate

Legend Biotech US -
Raritan, NJ

Apply Now

Job Details

Full-time
$59,168 - $77,658 a year

Qualifications

Laboratory procedures
Basic math
Sterile attire donning

Full Job Description

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life-threatening diseases. Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy through a portfolio of innovative technologies, including autologous, allogeneic, and in vivo cell therapy approaches. Our research spans chimeric antigen receptor T-cell (CAR-T), T-cell receptor (TCR-T), natural killer (NK) cell-based therapies, and other emerging platforms designed to transform the treatment of serious diseases. From our global network of research and development sites, we are committed to discovering and developing safe, effective, and cutting-edge therapies for patients worldwide.

Legend Biotech entered into a global collaboration agreement with Johnson & Johnson to jointly develop and commercialize CARVYKTI® (ciltacabtagene autoleucel; cilta-cel). Through this strategic partnership, we combine complementary expertise and capabilities to advance innovative immunotherapies for patients living with multiple myeloma.

Legend Biotech is seeking an Operations Associate (2nd Shift) as part of the Technical Operations team based in Raritan, NJ.

Role Overview

This position is responsible for performing manufacturing procedures and the execution of scheduled tasks within a CGMP environment. This position is responsible for quality and maintaining the highest standards in compliance within company policies, procedures, and all applicable regulations.

Key Responsibilities

Be part of the manufacturing operations team responsible for production of autologous CAR-T products for clinical and commercial operation in a controlled current Good Manufacturing Practice (cGMP) cleanroom environment.
Independently execute manufacturing or manufacturing-support processes according to standard operating procedures and current curriculum.
Execute manufacturing activities common to cell culturing, purification, aseptic processing, and cryopreservation using appropriate techniques.
Perform process unit operations according to standard operating procedures and batch records, and record production data and information in a clear, concise, format according to Good Documentation Practices (GDP).
Perform tasks on time in a manner consistent with quality systems and cGMP requirements.
Work in a team based, cross-functional environment to complete production tasks required by shift schedule.
Aid in the development of manufacturing processes including appropriate documentation.
Drive continuous improvement of manufacturing operations leveraging own observation as well as input of team members.
Handle human derived materials in containment areas.
Support schedule adjustments to meet production.
Accurately complete documentation in SOP's, logbooks and other GMP documents.
Demonstrate training progression through assigned curriculum.
Accountable for maintaining a working knowledge of basic cGMP requirements to ensure adherence to compliance policies and regulations
Wear the appropriate PPE when working in manufacturing and other hazardous working environments.
Proactively maintain a clean and safe work environment. Take necessary action to eliminate safety hazards and communicate to others any observed unsafe behaviors.
Ensure materials are available for production.
Job duties performed routinely require exposure to and handling of biological materials and hazardous chemicals
Distance visual acuity of at least 20/40 (Snellen) in both eyes without corrective lenses or visual acuity corrected to 20/40 (Snellen) or better with corrective lenses.
Color Perception both eyes 5 slides out of 8.
Report to work on-time and according to the shift schedule.
Perform other duties as assigned.
Attend departmental and other scheduled meetings.
Practice good interpersonal and communication skills.
Demonstrate positive team-oriented approach in the daily execution of procedures.
Promote and work within a team environment.
Learn new skills, procedures and processes as assigned by management and continue to develop professionally.
Support investigation efforts as required.
Responsible for audit preparation and participation.

Requirements

HS Diploma required with 3 – 5 Years Biotech/Pharmaceutical experience or equivalent industry experience // OR // Associates Degree required in Life Sciences or Manufacturing with 2 - 3 years of related experience // OR //Bachelors Degree required in Life Sciences with 0 - 2 years Biotech/Pharmaceutical experience or equivalent industry experience.
Interpret a variety of instructions furnished in written, oral, diagram or schedule form.
Follow instructions.
Solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.
Add, subtract, multiply and divide in all units of measure, using whole numbers, common factions, and decimals.
Knowledge and ability to operate manufacturing, manufacturing-support and lab equipment.
Knowledge of Process Excellence Tools
Possesses solid knowledge of routine and non-routine testing and sampling methods, techniques and related equipment.
Needs to be mobile and able to independently transport themselves between various sites/locations, as dictated by the essential functions and responsibilities of the position.
Is frequently required to communicate with coworkers.
While performing the duties of this job, the employee is regularly required to stand; walk; climb, bend and stoop; and reach with hands and arms.
Ability to lift 25 lbs.
Needs to perform gowning procedures to work in manufacturing core.

#Li-RN1

#Li-Onsite

Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.

Work Authorization & Employment Eligibility

Applicants must be authorized to work in the United States. As part of our commitment to maintaining a lawful workforce and ensuring compliance with federal employment regulations, we participate in the E-Verify program. If you are selected for employment, you will be required to complete the Form I-9 process, and your employment eligibility will be verified through E-Verify in accordance with applicable federal law. We are committed to providing a fair, transparent, and welcoming hiring experience for all candidates.

EEO Statement

It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances.

Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company.

For information related to our privacy notice, please review: Legend Biotech Privacy Notice.

Apply Now

Refine Your Search

production associate jobs in dunellen nj

Operations Associate

Manufacturing Upstream Associate I/II

Robotics Warehouse Associate

Production Associate - Builder/Material Handler

Picker (Warehouse Associate)

Manufacturing Downstream Associate I/II

Production Associate

IPQA Associate I

Packaging Associate I

Quality Assurance Associate

Post Harvest Associate

Quality Control (QC) / Production Associate I (Chemist)

Associate, Manufacturing (Helper)

Production Associate

Quality Control Associate

Associate Scientist, MSAT (Cell & Gene Therapy)

Compliance Associate II

Temp Conversion - Warehouse Associate - SUN-WED - 7:00 PM - 5:30 AM OB

Associate Supervisor, Quality

Production Associate – 2nd Shift

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