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Production Operator

Job in Chantilly, Fairfax County, Virginia, 22021, USA
Listing for: National Society of Professional Surveyors
Full Time position
Listed on 2026-03-07
Job specializations:
  • Manufacturing / Production
    Manufacturing Production, Operations Engineer, Quality Engineering, Production Associate / Production Line
Salary/Wage Range or Industry Benchmark: 60000 USD Yearly USD 60000.00 YEAR
Job Description & How to Apply Below

Position Title

Production Operator I - III (Solid Dosage/OSD Manufacturing)

Location

Chantilly, VA

Job Type
  • Manufacturing Job Type: Full-time
Shift Availability
  • 1st Shift: 7:00 am - 3:30 pm EST
  • 2nd Shift: 3:00 pm - 11:30 pm EST
  • Training:
    Must be available for training from 8:30 am - 5:00 pm EST for one month.
Job Summary

The Production Operator is responsible for tasks associated with drug product processing, ensuring adherence to current Good Manufacturing Practices (cGMPs), customer specifications, and Standard Operating Procedures (SOPs). Tasks may vary in complexity, scope, and sequence, and the role requires recognizing issues to improve efficiency, throughput, and quality. Operators manage production schedules and contribute to troubleshooting process issues, ensuring safe, efficient operations.

Key Responsibilities Production
  • Operate pharmaceutical production machinery, following procedures for manufacturing activities such as weighing, blending, dispensing, mixing, granulating, drying, compressing, and encapsulating.
  • Adhere to SOPs to ensure material purity and proper equipment usage.
  • Verify materials against Product s, QC release tags, and Batch Production Records.
  • Clean and perform machine changeovers, conduct in-process product quality checks, and document results accurately.
  • Follow assigned schedules and participate in debriefs to address any production issues.
Documentation
  • Maintain accurate documentation of manufacturing processes in batch records, logbooks, and protocols.
  • Complete and attach verification tickets, updating status boards as needed.
Continuous Improvement
  • Assist in troubleshooting, participate in improvement projects, and address deviations with the supervisor.
Safety & Compliance
  • Comply with all cGMP, SOP, policy, and safety requirements.
  • Participate in safety meetings and maintain a clean, organized work area.
Training
  • Fulfill all training requirements, including machine-specific training.
Teamwork & Collaboration
  • Share knowledge with team members, contributing to the overall success of projects and initiatives.
Requirements Trainee - Level I Operator
  • High school diploma, GED, or Associate Degree.
  • 1-3 years of experience in a physically demanding environment.
  • Proficiency in English (verbal and written).
Level II Operator (OSD/Solid Dose Manufacturing Experience Required)
  • High school diploma, GED, or Associate Degree.
  • 3-7 years of experience in OSD pharmaceutical manufacturing.
  • Forklift certification may be required for specific roles.
Level III Operator (OSD/Solid Dose Manufacturing Experience Required)
  • High school diploma, GED, or Associate Degree.
  • 7+ years of pharmaceutical manufacturing experience, with relevant certification or demonstrated proficiency.
Required Knowledge & Skills For Levels II & III
  • Experience in solid dose manufacturing (OSD) and equipment operation.
  • Proficiency in areas like Compression, Granulation, Encapsulation, Coating, etc.
  • Familiarity with FDA regulations, GMP, Lean Manufacturing, and Six Sigma principles.
  • Basic math, reading, and problem-solving skills.
  • Ability to participate in Continuous Improvement projects.
Physical Requirements
  • Ability to stand for extended periods, lift at least 50 pounds, climb ladders, wear a respirator, and all required PPE (safety glasses, earplugs, safety shoes).

Apply if you’re eager to contribute to high-quality production in a regulated environment with opportunities for growth.

Send us an email to  and tell me why you’re interested.

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