Top 67 Manufacturing specialist Jobs in Raritan Nj

Manufacturing Support Services Specialist
Cellares —Bridgewater, NJ
- $28 - $38 an hour
- Full-time
- Mid-level
- Forklift
- Analysis skills
Cell Therapy Manufacturing Specialist
Cellares —Bridgewater, NJ
- $20 - $45 an hour
- Full-time
- Mid-level
- Analysis skills
- Bachelor's degree
- Health insurance
- Dental insurance
QA Product Complaint Specialist
Insmed Incorporated —Bridgewater, NJ
- $81,000 - $103,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Engineering
- Employee stock purchase plan
- Disability insurance
Continuous Improvement & Lean Expert – Container Assembly
INNIO —Trenton, NJ
- Engineering
- Mid-level
- Communication skills
Quick Apply
Quality Specialist
MRP Solutions —Township of Franklin, NJ
- $24 - $26 an hour
- Full-time
- Mid-level
- Ability to climb stairs
- Analysis skills
Quick Apply
5d
Consumer Electronics Specialist – Testing & Sales
Paymore Matawan —Matawan, NJ
- $20 - $22 an hour
- Full-time
- Computer literacy
- Research
- Windows
Quick Apply
Validation Specialist -- Aseptic Operations
Interact Engineering LLC —Whippany, NJ
- $45 an hour
- Temporary
- Microsoft Excel
- Microsoft Outlook
- Engineering
Quick Apply
7d
Graphic Designer / Large Format Print & Sign Production Specialist
Signs By Tomorrow —Iselin, NJ
- $25 - $36 an hour
- 8 hour shift
- Hybrid work
- Mid-level
- Assembly
- Ability to lift 50 pounds
- Health insurance
- Dental insurance
Quick Apply
5d
Senior Quality Specialist (Document Control and Record Management)
Insmed Incorporated —Bridgewater, NJ
- $100,000 - $126,500 a year
- Full-time
- Hybrid work
- Office
- 3 years
- Bachelor's degree
- Employee stock purchase plan
- Disability insurance
13d
Quality Assurance Specialist-Junior
Stellar IT Solutions LLC —Bridgewater, NJ
- $35 - $42 an hour
- Microsoft Excel
- Writing skills
- English
Quick Apply
QA Shop Floor Specialist II
Legend Biotech US —Raritan, NJ
- $96,267 - $126,351 a year
- Weekends as needed
- Basic math
- Mid-level
- Microsoft Office
Quick Apply
Specialist, Documentation
USPL NUTRITIONALS LLC —North Brunswick, NJ
- $65,000 - $75,000 a year
- Full-time
- Writing skills
- English
- Mid-level
- AD&D insurance
- Paid holidays
Quick Apply
QA Stability Specialist
Amneal Pharmaceuticals —Branchburg Township, NJ
- $60,000 - $85,000 a year
- Full-time
- Bachelor of Science
- Microsoft Office
- 3 years
- Health insurance
- 401(k) matching
Manufacturing Quality Assurance (MQA) Specialist I, II, & III
Kashiv BioSciences, LLC —Piscataway, NJ
- $70,000 - $95,000 a year
- Full-time
- English
- Mid-level
- Continuous improvement
- Travel reimbursement
- Health savings account
Manufacturing QMS Specialist
Kashiv BioSciences, LLC —Piscataway, NJ
- $70,000 - $100,000 a year
- Full-time
- Microsoft Word
- 5 years
- Computer literacy
- Travel reimbursement
- Health savings account
Specialist, Documentation
US Pharma Lab —North Brunswick, NJ
- Full-time
- Writing skills
- English
- Mid-level
- AD&D insurance
- Paid holidays
Senior Quality Validation Specialist
Cellares —Bridgewater, NJ
- $90,000 - $210,000 a year
- Full-time
- Senior level
- 2 years
- Commercial
- Health insurance
- Dental insurance
Quality Systems Specialist
Katalyst Healthcares & Life Sciences —Branchburg, NJ
- Contract
- 5 years
- Senior level
Quick Apply
Associate Specialist, Value Stream Cryo Operations
Bristol-Myers Squibb —Summit, NJ
- $31.90 - $38.65 an hour
- Weekends as needed
- Hybrid work
- Ability to walk for extended periods
- Basic math
- No experience needed
- Paid holidays
- Disability insurance
5d
Quality Assurance (QA) Specialist I, II, & III
Kashiv BioSciences, LLC —Piscataway, NJ
- $70,000 - $95,000 a year
- Full-time
- English
- Mid-level
- Warehouse
- Travel reimbursement
- Health savings account

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Manufacturing Support Services Specialist

Cellares
Bridgewater, NJ

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Job Details

Full-time
$28 - $38 an hour

Qualifications

Biotechnology
Safety training program participation as safety practice
Manufacturing standard operating procedures
Manufacturing facility experience
Quality assurance standard operating procedures
Laboratory standard operating procedures
Safety standard operating procedures
Factory experience
Standard operating procedures (SOPs)
Standard operating procedures drafting
Pharmaceutical manufacturing facility experience

Full Job Description

Position Summary

Night Shift: 6 PM- 6 AM

We are seeking an innovative and highly motivated Manufacturing Support Services Specialist to join our Operations team who will contribute to the manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day warehouse operations. This is a hands-on position that will train in the Manufacturing and Warehouse Team.

Candidates should enjoy working in a fast-paced, mission-driven environment and be prepared to tackle a broad selection of challenges as the company grows.

Responsibilities

Perform routine procedures following written instructions (SOPs, batch records, solution documents, protocols, etc.)
Execute basic manufacturing processes in a GMP environment, e.g., buffer or media preparation, usage of controlled rate freezers, and LN2 tanks
Support sample management and transport using LIMS
Support Warehouse team with receiving of inbound consumables, labeling, and put-away using SAP and label printers
Operate a forklift to accomplish warehouse duties
Supports the maintenance and supply of warehouse storage
Perform routine clean room and laboratory activities, including ordering of consumables and PPE items, cleaning, restocking, and equipment qualification/maintenance
Operate in a controlled GMP environment and perform gowning as per procedure
Complete required training and ensure compliance with established internal and external control procedures
Responsible for revising and originating production records and standard operating procedures
Initiate and support the closure of Deviation Reports and CAPAs
Train and mentor new manufacturing support services associates on procedures, aseptic techniques, equipment, and troubleshooting skills
Review in-process and completed documents for accuracy and to make sure batch records are turned in to area management within the specified days of completion
Provide user feedback to engineering and process teams, support with requirements gathering and review
Work with Quality Control, Facilities, Materials Management, Quality Assurance, and Validation to complete assignments
Other duties as assigned

Requirements

Bachelor’s Degree or a diploma in a scientific or related field is preferred
1-2 years of experience within the biotech/biopharma industry in cGMP Operations, preferably within cell and gene therapy
Must know and follow job safety procedures, attend required health and safety training, proactively promote safety at work, and promptly report actual and potential accidents and injuries.
Must comply with the safety policies of the company and site
Ability to lift 30 pounds
Adherence to cGMPs is required at all times during the manufacturing of Cell Therapy products
SAP and LIMS experience is preferred
Proficiency in Drug Product-related process equipment
Must have experience following protocols, SOPs, and/or GMP documentation
Excellent verbal, written, presentation, and interpersonal skills
Strong analytical and problem-solving skills
Self-motivated and passionate about advancing the field of cell therapy
Self-awareness, integrity, authenticity, and a growth mindset
Desire to be part of a rapidly evolving organization, with compelling technology, and take products and processes to the next level

$28 - $38 an hour

This is Cellares

Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company’s Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares’ Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.

The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing.

Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Apply Now

Refine Your Search

manufacturing specialist jobs in raritan nj

Manufacturing Support Services Specialist

Cell Therapy Manufacturing Specialist

QA Product Complaint Specialist

Continuous Improvement & Lean Expert – Container Assembly

Quality Specialist

Consumer Electronics Specialist – Testing & Sales

Validation Specialist -- Aseptic Operations

Graphic Designer / Large Format Print & Sign Production Specialist

Senior Quality Specialist (Document Control and Record Management)

Quality Assurance Specialist-Junior

QA Shop Floor Specialist II

Specialist, Documentation

QA Stability Specialist

Manufacturing Quality Assurance (MQA) Specialist I, II, & III

Manufacturing QMS Specialist

Specialist, Documentation

Senior Quality Validation Specialist

Quality Systems Specialist

Associate Specialist, Value Stream Cryo Operations

Quality Assurance (QA) Specialist I, II, & III

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