Manufacturing Operator Actalent East Windsor, NJ

• On-Site Apply Visionary Operations Data Entry Innovation Mathematics Hand Writing Process Safety Pharmaceuticals Word Processing Experimentation Quality Assurance State Regulations Process Development Process Engineering Equipment Operation Inductive Reasoning Chemical Engineering Operational Databases Packaging And Labeling Regulatory Requirements Product Quality (QA/QC) Research And Development Engineering Design Process Verbal Communication Skills Training Records Management Standard Operating Procedure Good Manufacturing Practices Good Documentation Practices Pharmaceutical Manufacturing Personal Protective Equipment Continuous Improvement Process Troubleshooting (Problem Solving) Continuous Quality Improvement (CQI) Current Good Manufacturing Practices (cGMPS) At least 2 years STARs-friendly $54,080 - $62,400 / yr Posted yesterday This role is

STARs-friendly:

Skilled Through Alternative Routes. 73 % STARs in role.

Description:

Job Title:

Manufacturing Operator Job Description This role is responsible for operating pharmaceutical manufacturing equipment in a regulated GMP environment to produce clinical supplies and support development experiments. The manufacturing operator follows established procedures, maintains high-quality documentation, and works closely with quality, maintenance, and development teams to ensure safe, compliant, and efficient production. Responsibilities Train on and 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 other regulated manufacturing environment, adhering to batch records and Good Documentation Practices (GDP). Set up, operate, change over, and clean pharmaceutical manufacturing equipment and rooms according to SOPs and work instructions. Execute line setup and line clearance activities to ensure equipment and work areas are properly prepared and documented before production. Perform in-process inspections and sampling to verify product quality and process performance, documenting results accurately and in a timely manner. Use appropriate personal safety equipment and engineering controls to protect personnel, products, and equipment. Operate within an IT platform to enter, review, and track production data and related documentation. Perform developmental manufacturing experiments under the direction of a formulation specialist or process engineer to support process development and optimization. Support investigational and quality systems activities, including deviation support, corrective actions, and continuous quality improvement initiatives. Assist maintenance personnel with preventive maintenance activities, basic troubleshooting, and repair support for manufacturing equipment. Participate in continuous improvement activities by making suggestions for process, safety, or efficiency enhancements and by adopting new skills and procedures. Carry out all duties in compliance with applicable federal and state regulations, guidelines, and internal company and site policies. Remain current with industry trends and professional best practices relevant to pharmaceutical manufacturing and GMP operations. Complete required regulatory and job-specific training and maintain training records in good standing. Perform repetitive tasks while maintaining production speed, accuracy, and attention to detail. Work effectively as part of a team, collaborating with colleagues in production, quality, engineering, and other functions. Be available for additional duties as required and for overtime as needed to meet production and project timelines. Essential Skills Associates degree and at least 2 years of experience in GMP pharmaceutical manufacturing, research and development, or pharmaceutical equipment manufacturing. Experience working in a GMP or regulated manufacturing environment with a strong understanding of compliance and quality expectations. Hands-on experience with batch records and Good Documentation Practices (GDP), including batch record review and accurate documentation of manufacturing activities. At least 2 years of experience in batch record review, quality assurance operations, and line clearance activities. Pharmaceutical or contract development and manufacturing organization (CDMO) GMP experience in production or chemical manufacturing involving equipment operation and SOP-driven processes. Knowledge of current Good Manufacturing Practices (cGMP) and familiarity with pharmaceutical manufacturing processes. Experience as a manufacturing operator or packaging technician in a regulated environment. Ability to read and interpret SOPs, manuals, batch records, work instructions, and specifications. Clear written and oral communication skills, including legible handwriting and the ability to document work accurately. Basic mathematical skills, including addition, subtraction, fractions, percentages, ratios, and proportions, and the ability to apply these concepts to practical manufacturing tasks. Ability to identify simple to moderate problems related to job functions and apply deductive and inductive reasoning to reach sound conclusions. Proficiency with computer applications for data entry, word processing, and email communication. Ability to perform repetitive tasks while maintaining high levels of accuracy, speed, and attention to detail. Ability to work collaboratively in a team environment and support shared production and quality goals. Additional Skills & Qualifications Degree in a scientific discipline or chemical engineering is strongly preferred. Familiarity with pharmaceutical manufacturing equipment and processes, including room and equipment setup, operation, and cleaning. Experience working around quality assurance and compliance requirements, including exposure to investigational and quality systems activities. Demonstrated ability to successfully complete regulatory and job-specific training requirements. Comfort working within IT platforms to enter and manage production data and documentation. Willingness to learn new skills, procedures, and processes and to contribute ideas for continuous improvement. Ability to remain current with professional and industry trends relevant to pharmaceutical manufacturing. Flexibility to support overtime or additional responsibilities as production needs evolve. Strong attention to safety, including consistent use of personal protective equipment and adherence to engineering controls. Job Type & Location This is a Contract to Hire position based out of East Windsor, NJ. Pay and Benefits The pay range for this position is $26.00 - $30.00/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) Workplace Type This is a fully onsite position in East Windsor,NJ. Application Deadline This position is anticipated to close on Oct 5, 2026. 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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JP-006313383