Manufacturing Operator

Actalent; Cranbury Township (NJ); On-site; USD 33,000 - 36,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

401(k)

Job summary

Actalent is seeking a Manufacturing Operator in Cranbury, NJ, to operate pharmaceutical manufacturing equipment in a cGMP environment. This role involves batch record handling, equipment setup and cleaning, and strict adherence to regulatory, safety, and quality standards.

You will work in a growing CDMO with modern facilities and participate in development experiments and continuous improvement initiatives while supporting production demands and overtime as needed.

Qualifications

• Associates Degree and two years of experience in GMP pharmaceutical manufacturing or related field.
• Experience in a GMP or regulated pharmaceutical manufacturing environment, with QA/compliance familiarity.
• At least 1 year of experience with batch record review, QA operations, and line clearance activities.

Responsibilities

• Train on and understand all policies, procedures, SOPs, work instructions, and related documentation.
• Perform pharmaceutical manufacturing activities in a GMP environment following established processes and quality standards.
• Complete and maintain batch records and GDP in compliance with cGMP requirements.
• Set up, operate, and perform changeovers on lines to ensure readiness for production.
• Perform equipment set‑up, operation, and cleaning per SOPs and procedures.
• Use PPE and engineering controls to perform tasks safely and in compliance with safety policies.
• Conduct in‑process inspections and sampling, document results as required.
• Enter data and communicate via designated IT platforms and systems.
• Support developmental manufacturing experiments to aid process/product development.

Skills

GMP manufacturing

Batch records

Equipment operation

GDP knowledge

Education

Associate degree

Job description

Job Title: Manufacturing OperatorJob Description

The 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 Environment

This 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 & Location

This is a Contract position based out of Cranbury, NJ.

Pay and Benefits

The 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)

Application Deadline

This position is anticipated to close on Nov 13, 2026.

Workplace Type

This 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 [e-mail] 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.