QC Technician

Actalent, Inc.; Greenville (NC); On-site; USD 28,000 - 36,000; Full time

Job description

Job Title: QC Technologist

Job Description

A successful candidate will perform Environmental Monitoring tasks in support of Steriles production within classified areas. The individual is encouraged to follow the company’s core values: integrity, innovation, intensity, and involvement. The job requires knowledge of aseptic gowning and working in cleanrooms to monitor areas where sterile products are filled and manufactured. Typical shift hours are 6 PM to 6 AM on a 2-2-3 rotating schedule.

• Perform analyses including instrumental and automated methods using prescribed procedures and techniques.
• Generate valid data, report results on appropriate database compared to established specifications while adhering to GMPs.
• Compare laboratory results with specifications for acceptability and determine if repetition or OOS is required.
• Maintain equipment and troubleshoot instrumentation problems, procedural problems, or production problems.
• Review and understand SOPs and analytical procedures as needed.
• Schedule activities to meet target dates for customer needs.
• Follow all job-related safety and other training requirements.
• Perform tasks as assigned by area supervision or designee.
• Able to withstand extended periods of standing and/or walking and bending.

• High school diploma including laboratory work in a science discipline. An associate's degree in a science-related field, preferably Biology, is preferred.
• 1 year related experience preferred performing lab bench work including utilizing instrumentation and reporting data.
• Knowledge of aseptic techniques.
• Knowledge of MS Excel and Word and familiarity with using each program.
• Excellent problem-solving and critical thinking skills.
• Organization and detailed planning skills.
• Strong attention to detail and ability to follow standard procedures.
• Good knowledge of quality and regulatory requirements in the pharmaceutical industry, including pharmaceutical GMPs.
• Good interpersonal and communication skills (both oral and written).
• Ability to apply mathematical operations.

• Relevant post-secondary educational courses.
• Ability to thrive in a fast-paced, constantly evolving environment.

This position primarily focuses on production line support and involves extended periods of standing, walking, stooping, kneeling, squatting, and crouching. The role requires the ability to lift, carry, and/or move weights of 25-50 pounds, and occasionally push or pull 50-100+ pounds. Dexterity in arms, hands, and fingers is necessary, including the ability to grasp and type for prolonged periods. Visual acuity is required for using a keyboard, computer monitor, operating equipment, and reading materials. The position also requires the ability to sit, reach with hands and arms, talk, and hear for extended periods. Ordinary ambulatory skills and physical coordination are needed to move about the environmental lab.

Job Type & Location

This is a Contract position based out of Greenville, NC.

Pay & Benefits

The pay range for this position is $23.00 - $23.00/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.

• 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)

Workplace Type

This is a fully onsite position in Greenville,NC.

Application Deadline

This position is anticipated to close on Apr 4, 2025.

Equal Opportunity Employer 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 [e-mail] for other accommodation options.