Jobs in the United States

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LAW ENFORCEMENT INVESTIGATOR II - 43001782
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MIAMI, FL
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Summer 2027 UCD Reporting and Analytics Undergraduate Intern
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Remote, United States
…presentations using team-approved analytical and reporting…
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(Remote) Corporate Development Sales Associate
N. Harris Computer Corporation - USA
Remote, United States
- $65,000 to $80,000 USD / year
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Lube Technician
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Follow Meineke's standard operating procedures and safety guidelines while handling tools, equipment, and vehicle systems.
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HR Coordinator
IAVI
Jersey City, NJ · New York, NY · San Diego, CA
- $25 to $30 USD / hour
Proficiency with Microsoft Office and comfort learning HR systems, digital tools, and AI-enabled productivity tools.
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Commercial Cleaner - Laurel & Catonsville
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Using ServiceMaster products and tools to ensure spotless results.
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Commercial Cleaner - Cockeysville/Lutherville
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Senior Product Manager – Prediction Markets & US Sports Data
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New York, NY
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Talent Acquisition Operations Intern - Spring 2027
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Actalent

Quality Operator

Portage, IN, United States

$20 USD / hour

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Job details

Pay: $20 USD / hour
Posting language: English
Posted: Nov 9, 2026

Original job description

Job Title: Quality Operator 2nd ShiftJob DescriptionThe Quality Operator on 2nd shift (MondayFriday, 4:00 p.m. to 12:00 a.m.) sets up, operates, adjusts, and changes over packaging line equipment in a regulated pharmaceutical manufacturing environment. This role ensures continuous packaging operations by supplying materials, monitoring product quality attributes, performing in-process checks, and accurately documenting results in accordance with Good Manufacturing Practices (GMP). The Quality Operator also performs minor mechanical adjustments, participates in cleaning and validation activities, and supports cross-functional trials to maintain high standards of product quality and operational efficiency.Responsibilities

Set up, adjust, operate, and perform changeovers on packaging machinery to support continuous production runs.
Start packaging equipment and closely observe operations to detect mechanical or operational malfunctions.
Stop equipment when issues arise and promptly report malfunctions to the Production Supervisor or appropriate personnel.
Analyze mechanical or operational problems, determine root causes, and take appropriate corrective actions within defined procedures.
Test and verify equipment performance after changeovers to ensure quality operation before returning to production.
Monitor and inspect product during packaging to confirm it meets all specifications and quality standards.
Measure and track product variables and attributes throughout the production run to ensure designated parameters are maintained.
Document in-process testing results, batch progress, and equipment activities accurately and on time in the Packaging Batch Record and other GMP documentation.
Comply with all internal policies and procedures, as well as applicable FDA, DEA, OSHA, and other regulatory requirements.
Maintain a clean, organized, and safe work area, following all housekeeping and safety guidelines.
Perform required facility and equipment cleaning in accordance with the master cleaning schedule and cleanroom requirements.
Assist with equipment and process validation efforts, including setup, execution support, and documentation as needed.
Support Research and Development, Manufacturing Technology, and engineering teams during trials and studies on the packaging line.
Collaborate effectively with production, quality, and other team members to meet production, quality, and safety goals.
Use computer/PLC-controlled systems to input and monitor machine settings, track performance, and support troubleshooting activities.

Additional Skills & Qualifications

Associates degree or equivalent from a two-year college or technical school is acceptable.
Experience in the sciences is preferred, particularly for candidates interested in progressing into quality or laboratory roles over time.
Experience in a manufacturing, production, or general labor environment is beneficial.
Previous exposure to GMP, FDA-regulated, or pharmaceutical manufacturing environments is an advantage.
Strong people skills and the ability to work effectively within a tight-knit, collaborative team.
Demonstrated ability to prioritize tasks, stay organized, and maintain high accuracy in a fast-paced setting.
Interest in learning pharmaceutical industry regulations and best practices, with a desire to grow into roles in QA, manufacturing quality assurance, or laboratory/office functions.
Comfort working with computer-based systems and automated equipment in a production setting.
Ability to identify recurring equipment issues and communicate insights to management to support continuous improvement.

Job Type & LocationThis is a Contract to Hire position based out of Portage, IN. Pay and BenefitsThe pay range for this position is $20.00 - $20.00/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 to Hire position based out of Portage, IN. Application DeadlineThis position is anticipated to close on Nov 23, 2026. Workplace TypeThis is a fully onsite position in Portage,IN.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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More about this job

Skills

Good manufacturing practices
Packaging
Documentation
Housekeeping
Brush the equipment
Cleaning
Research
PLC
Troubleshooting
Pharmaceutical processes
Prioritization
Pharmaceutical industry
Quality assurance
Process improvement

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