Jobs in the United States

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PRODUCT DEVELOPMENT TEST TECHNICIAN
Vybond
Franklin, KY
The Product Development Test Technician is responsible for executing laboratory testing and preparing lab-scale samples to support research, new product development, product improvement,…
Added 1 min ago
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ATD MIHL Equipment Development Engineer
Intel Corporation
AZ
- $99,030 to $188,890 USD / year
Join Intel's Packaging Module Development team as a Packaging Module Development Engineer and contribute to advancing innovative assembly and packaging technologies. In this role, you will…
Added 1 min ago
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GPU Software Architect
Intel Corporation
CA
- $233,990 to $330,340 USD / year
As a Principal Engineer specializing in GPU Software Architecture, you will lead the design and development of cutting-edge software solutions for Intel GPUs. In this role, you will…
Added 2 mins ago
Associate Structural Engineer (Buildings)
WSP
New York, NY · NY
WSP is currently initiating a search for an Associate Structural Engineer for our New York, NY office. Be involved in projects with our Property and Buildings Team and be a part of a…
Added 3 mins ago
Instructor - HVAC Building Management and Maintenance (Northlands)
Erie Community College
United States
PROFESSIONAL DEVELOPMENT – Regular internal professional development events and offerings, funding available for conferences and travel, participation in seminar offerings, business and…
Added 6 mins ago
Principal Engineer I - System Design / Architecture Engineering
Toyota
Liberty, NC
…Department is seeking a highly motivated Infrastructure / Platform Engineer to support the implementation, reliability, and operational excellence of infrastructure and platform…
Added 6 mins ago
Production Engineer
Toyota
Georgetown, KY
The primary responsibility of this role is to ensure vehicle/process integrity through systems development and process management within the Unit Weld or Plastics shops.
Added 7 mins ago
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Principal Validation Engineer
Pfizer, Inc.
MA
- $124,400 to $207,400 USD / year
The Principal Validation Engineer under Andover Site Technical Services (STS) is the principal owner of the Pfizer (PGS) Andover site validation program and master plan. The incumbent is…
Added 8 mins ago
Senior Spacecraft Operations Engineer II- Secret Clearance
Rocket Lab Corporation
Long Beach, CA
…Moon and Mars, working with partners including NASA, the Space Development Agency, and the U.S. Space Force. Whether it’s a single high-performance spacecraft, constellation, or the…
Added 9 mins ago
Specialist, Engineering
Merck Sharp & Dohme LLC
PA
…production and/or final formulation and filling operations. This engineer will be a member of the Technical Services Deviation Management team in the Live Virus Vaccine Manufacturing…
Added 10 mins ago
Business Operations Analyst - Strategy
AFL
Duncan, SC
…and approved information sources, coordinates the response process, and prepares clear, accurate, and appropriately detailed…
Added 11 mins ago
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Construction Project Manager
TEKsystems
Indianapolis, IN
- $90,000 to $120,000 USD / year
Serve as the primary point of contact for clients throughout the design-build process.
Added 11 mins ago
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Construction PM
TEKsystems
Columbus, OH
- $90,000 to $120,000 USD / year
…This individual will oversee all phases of the design-build process, serving as the primary point of contact for clients while coordinating internal teams, subcontractors, and stakeholders…
Added 11 mins ago
Embedded C++ Software Engineer (5808) (Broomfield, CO) (Abil to obtain Secret)
Outside Analytics
Broomfield, CO
The remote sensing world is expanding and we’re building our team to grow with it. We are seeking an Embedded Software Engineer with a strong background in C++ to join our small, dynamic,…
Added 19 mins ago
Senior Software Engineer Technical Remediation & Enablement
Citi
NY · New York
The Applications Development Technology Lead Analyst is a senior level position responsible for establishing and implementing new or revised application systems and programs in coordination…
Added 20 mins ago
Mechanical Engineer III
JLABHCM20
Newport News
…technical oversight of the contractor through the fabrication process. Give effective presentations to various audiences, write convincing proposals and reports with all necessary backup…
Added 22 mins ago
Electrical Superintendent - Solar - Louisiana
Black & Veatch Family of Companies
Bogalusa, LA
Assists the Construction Engineer in the compilation or answering of Contractor Information Requests.
Added 22 mins ago
Product Development Engineer - Heat Exchanger Core Engineer
Ford Global
Dearborn, MI
Product Development uses design thinking & user experience methods to deliver breakthrough products and services that delight our customers. We bring innovative, exciting, and sustainable…
Added 22 mins ago
Product Development Engineer - Evaporator & Blower Assembly (HVAC) Core Engineer
Ford Global
Dearborn, MI
Product Development uses design thinking & user experience methods to deliver breakthrough products and services that delight our customers. We bring innovative, exciting, and sustainable…
Added 22 mins ago
Customer Identity Platform Engineer
Ford Global
Remote, United States
The Customer Identity Platform Engineer will contribute to the engineering, development, and 24/7 support of identity and access management highly available solutions for the customer…
Added 22 mins ago
Quality Systems Engineer II, (Quality, Day Shift Mon-Fri)
Panasonic North America
Sparks, NV
The Quality Systems Engineer Level 2 support / lead the development, implementation, maintenance, and continual improvement of the Quality Management System (QMS) in compliance with ISO…
Added 22 mins ago
Physicist/Scientist, Doctorate Degree, New College Grad (Spring 2027)
Applied Materials, Inc
Santa Clara, CA
Collaborate closely with experimental teams to guide process development and interpret new experimental results
Added 23 mins ago
Project Engineer
Aerotek
Menlo Park, CA
Job Title: Project EngineerJob DescriptionThe Project Engineer plans, organizes, and manages all document control and distribution processes for the Planning, Design & Construction (PD&C)…
Added 23 mins ago
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Maintenance Engineer
Aerotek
Plymouth, MN
- $34 to $42 USD / hour
Job Title: Maintenance Mechanic1st shift ($34-$42/HR)Job DescriptionThe Maintenance Engineer supervises and performs a wide range of maintenance activities, including predictive…
Added 25 mins ago
PRODUCT DEVELOPMENT TEST TECHNICIAN
VYBOND SPECIALTY ADHESIVES LLC
Franklin, KY
The Product Development Test Technician is responsible for executing laboratory testing and preparing lab-scale samples to support research, new product development, product improvement,…

Actalent

Manufacturing Operator

Cranbury, NJ, United States

$24 to $26 USD / hour

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Job details

Pay: $24 to $26 USD / hour
Experience: At least 1 year of experience with batch record review, QA operations, and line clearance activities.
Posting language: English
Posted: Oct 30, 2026

Original job description

Job Title: Manufacturing OperatorJob DescriptionThe Manufacturing Operator works under direct supervision to operate pharmaceutical manufacturing equipment in a cGMP environment to produce clinical supplies and support development experiments. This role involves hands-on work with batch records, equipment set-up and cleaning, and adherence to strict regulatory, safety, and quality standards. The position offers the opportunity to contribute to a rapidly growing contract manufacturing organization with a brand-new facility, modern equipment, and multiple new products in the pipeline.

Responsibilities

Train on and fully understand all applicable policies and procedures, including regulatory requirements, safety guidelines, standard operating procedures (SOPs), work instructions, and related documentation.
Perform pharmaceutical manufacturing activities in a GMP or regulated manufacturing environment, following established processes and quality standards.
Complete and maintain batch records and Good Documentation Practices (GDP) accurately, legibly, and in compliance with cGMP requirements.
Set up, operate, and perform changeovers on manufacturing and packaging lines, ensuring proper configuration and readiness for production.
Perform pharmaceutical equipment and room set-up, operation, and cleaning in accordance with SOPs and cleaning procedures.
Use appropriate personal safety equipment and engineering controls to perform all tasks safely and in compliance with safety policies.
Conduct in-process inspections and sampling to verify product quality and process performance, documenting results as required.
Use designated IT platforms and computer systems for data entry, documentation, and communication related to manufacturing activities.
Perform developmental manufacturing experiments under the direction of a formulation specialist or process engineer, supporting process and product development.
Support investigational and quality systems activities, including assisting with deviation investigations, corrective actions, and continuous improvement initiatives.
Assist maintenance personnel in performing preventive maintenance activities, troubleshooting, and repair of manufacturing equipment as needed.
Participate actively in continuous improvement activities by making suggestions for process, safety, and efficiency enhancements.
Carry out duties in compliance with all applicable federal and state regulations, as well as all company and site policies and procedures.
Remain current in professional knowledge and industry trends relevant to pharmaceutical manufacturing and cGMP requirements.
Learn new skills, procedures, and processes as needed to support changing production and development needs.
Perform other duties as required to support manufacturing operations and departmental objectives.
Be available for overtime as needed to meet production schedules and operational demands.

Essential Skills

Associates Degree and two (2) years of experience in GMP pharmaceutical manufacturing, research and development (R&D), or pharmaceutical equipment manufacturing.
Experience in a GMP or regulated pharmaceutical manufacturing environment, including familiarity with QA and compliance requirements.
At least 1 year of experience with batch record review, QA operations, and line clearance activities.
Hands-on experience as a manufacturing operator or packaging technician in a pharmaceutical or CDMO GMP setting.
Demonstrated experience with production, chemical processing, equipment operation, and adherence to SOPs in a pharmaceutical context.
Strong knowledge of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).
Ability to read and interpret documents such as SOPs, manuals, batch records, work instructions, and specifications.
Legible handwriting and the ability to complete documentation accurately and clearly.
Ability to communicate clearly both in writing and orally with colleagues and supervisors.
Basic mathematical skills, including addition, subtraction, fractions, percentages, ratios, and proportions, and the ability to apply these concepts to practical work situations.
Ability to identify simple and moderate problems related to job functions and apply deductive and inductive reasoning to resolve them.
Ability to perform repetitive tasks while maintaining required speed, accuracy, and attention to detail without loss of production.
Ability to work effectively with others in a team environment.

Additional Skills & Qualifications

Degree in a scientific discipline or chemical engineering is strongly preferred.
Experience in a CDMO (contract development and manufacturing organization) environment is highly desirable.
Familiarity with pharmaceutical manufacturing processes and equipment beyond basic training.
Successful completion of regulatory and job-specific training requirements, including safety and cGMP training.
Proficiency with computer applications for data entry and word processing, including the ability to enter data accurately into software systems.
Ability to work with and be proficient in email systems and IT platforms used for communication and documentation.
Demonstrated willingness to learn new skills, procedures, and processes to support evolving business needs.
Ability to make constructive suggestions for process, safety, and quality improvements.
Comfort working with quality systems and supporting investigational activities related to deviations, nonconformances, or process improvements.

Work EnvironmentThis role is based in a contract manufacturing organization focused on pharmaceutical products, operating in a modern, brand-new facility equipped with up-to-date manufacturing and processing equipment. The environment is fully cGMP-compliant and regulated, with a strong emphasis on quality, safety, and adherence to documented procedures. Employees handle and evaluate various samples and products under controlled conditions and work closely with quality and compliance functions. The position follows a first-shift schedule, typically from 7:00 a.m. to 3:30 p.m., with overtime available as needed to meet production demands. Work involves routine use of personal protective equipment and engineering controls, repetitive tasks requiring sustained attention to detail, and collaboration within a team-oriented setting. The organization is growing rapidly, with significant recent expansion, multiple new products being introduced, and a culture that encourages continuous improvement, professional development, and staying current with industry trends. Job Type & LocationThis is a Contract position based out of Cranbury, NJ. Pay and BenefitsThe pay range for this position is $24.00 - $26.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits

available for this temporary role may include the following:

Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave) Job Type & LocationThis is a Contract position based out of Cranbury, NJ. Application DeadlineThis position is anticipated to close on Nov 13, 2026. Workplace TypeThis is a fully onsite position in Cranbury,NJ.About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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