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TRS Staffing Solutions

TRS Staffing Solutions is hiring: Manufacturing Technician in Charleston

TRS Staffing Solutions, Charleston, SC, United States, 29408

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TRS Staffing Solutions provided pay range

This range is provided by TRS Staffing Solutions. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$24.00/hr - $38.00/hr

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Technical Recruiter at TRS Staffing Solutions, Engineering Recruitment Specialist (subsidiary of Fluor Corporation) with focused efforts in…

Location: Charleston, SC

Shifts:

2nd Shift | Monday – Friday | 3:00 PM – 11:30 PM [2 openings]

3rd Shift | Sunday – Thursday | 11:00 PM – 7:30 AM [2 openings]

Compensation: $24–$38/hour DOE + Shift Differential | Overtime possibilities

Benefits: Full Benefits Package | Paid Time Off | 401(k) | Relocation Assistance

Position Overview

We are seeking motivated and detail-oriented Manufacturing Technicians (Levels I–III) to join our growing team in Charleston, SC. In this role, you will support the production of pharmaceutical drug products (parenteral or solid dosage) for both commercial distribution and clinical trials.

You will operate manufacturing equipment, follow strict regulatory guidelines, and ensure compliance with current Good Manufacturing Practices (cGMPs).

This is a hands‑on role in a fast‑paced, highly regulated environment that requires precision, teamwork, and a commitment to quality.

Key Responsibilities

  • Operate manufacturing and material handling equipment in accordance with SOPs and cGMP standards.
  • Accurately document all activities in real‑time using controlled documentation systems.
  • Perform in‑process testing, weight checks, and basic calculations.
  • Clean and sanitize rooms, tools, and equipment to maintain a sterile environment.
  • Support cross‑functional manufacturing areas as needed.
  • Follow all safety protocols, including proper PPE gowning procedures.
  • Complete all required training in a timely and compliant manner.
  • Perform other duties as assigned.
  • Equipment and component preparation and sterilization
  • Compounding of sterile solutions
  • Aseptic filling operations
  • Capping and sealing processes

Qualifications

  • High school diploma or GED required; Associate’s or Bachelor’s degree preferred.
  • Minimum 1 year of experience in a GMP‑regulated environment (pharmaceutical, biotech, medical device, food services, or life sciences).
  • Strong verbal and written communication skills.
  • High attention to detail and organizational ability.
  • Basic troubleshooting and problem‑solving skills.
  • Ability to perform basic math and follow detailed written instructions.
  • Comfortable working with computers and digital documentation systems.
  • Familiarity with cGMP practices in an aseptic environment required.

Physical Requirements & Work Environment

  • Regularly required to stand, walk, reach, and use hands for extended periods.
  • Must be able to lift/move up to 25 lbs frequently and up to 50 lbs occasionally (with assistance).
  • Exposure to moving mechanical parts, airborne particles, and chemicals.
  • Use of PPE including safety glasses, gloves, respirators, and full-body coverings is mandatory.
  • May require working at heights or operating industrial vehicles.

Seniority level

Mid‑Senior level

Employment type

Full‑time

Job function

Manufacturing and Quality Assurance

Pharmaceutical Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

Tuition assistance

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