Production Operator

Scientific Search; Chantilly (VA); On-site; USD 40,000 - 60,000; Full time

Job summary

A prominent staffing agency in Virginia is looking for a Production Operator I - III in OSD Manufacturing. The role involves operating production machinery, adhering to standard operating procedures, and ensuring compliance with Good Manufacturing Practices (cGMP). Candidates should have relevant experience depending on the level, with opportunities for growth in this highly regulated environment. A high school diploma or equivalent is required, along with physical capability for handling production tasks.

Qualifications

• Must have a high school diploma or equivalent.
• 1-3 years of experience in a physically demanding environment.
• Experience in solid dose manufacturing and relevant certification for Levels II & III.

Responsibilities

• Operate and monitor pharmaceutical production machinery.
• Adhere to SOPs and ensure material purity.
• Maintain documentation of manufacturing processes.

Skills

Attention to detail

Proficiency in English (verbal and written)

Basic math skills

Education

High school diploma, GED, or Associate Degree

Tools

Pharmaceutical production machinery

Forklift (if applicable)

Job description

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

Location

Chantilly, VA

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

• 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 ID Labels, 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 [e-mail] and tell me why you’re interested.