Pharmaceutical Manufacturing Technician - 2nd Shift
Job
Overview
United States, North Charleston, South Carolina
- QA/QC
- Permanent
You are subscribed to our push notifications, but not currently for jobs like this.
Would you like to receive notifications for jobs like this as well?
Great news! You are subscribed to receive alerts for jobs similar to this one.
Location: Charleston, South Carolina
Shift: 2nd Shift | Monday – Friday | 3:00 PM – 11:30 PM
Compensation: $24–$38/hour + Shift Differential | Overtime Available
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
- 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 preferred.
- 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.
TRS Staffing Solutions are an equal opportunities employer, and we welcome you to provide OFCCP data voluntarily here
We are an equal opportunity employer. All qualified individuals will receive consideration for employment without regard to race; color; age; sex; sexual orientation; gender identity; religion; national origin; disability; veteran status; genetic information; or any other criteria protected by governing law.
Sign-up for Job Alerts
Our latest jobs
Negotiable
United States, North Charleston, South Carolina
Negotiable
United States, North Charleston, South Carolina
Negotiable
United States, North Charleston, South Carolina
Negotiable
United States, Ada, Oklahoma
PLN 20000
Poland, Gliwice, Slaskie
Negotiable
Denmark, Kulndborg , Capital Region
Negotiable
Netherlands, Regio Noord-Holland, Noord-Holland
Negotiable
Netherlands, regio Noord-Holland, Noord-Holland
Negotiable
United States, Greenville, South Carolina
Negotiable
Denmark, , Zealand Region
Our insights
.jpg)
