Pharmaceutical Manufacturing Technician II (DPI)
United Therapeutics Corporation
4 hours ago
On-site
Raleigh-Durham-Chapel Hill Area
Operations
Who you are
Pharmaceutical manufacturing professional with experience in upstream processes in a GMP environment. Handles raw materials, prepares and moves large-scale suspensions, and operates equipment such as tanks, mixers, and filtration systems. Maintains accuracy and compliance (weighing/dispensing materials and completing batch records), troubleshoots issues, collaborates on solutions, and takes process ownership to ensure upstream operations run seamlessly and support production of life-changing therapies.
Minimum Requirements
- H.S. Diploma or GED and 2+ years of relevant hands-on experience in a regulated production environment
- Strong cGMP documentation practices
- Experience with production equipment in a regulated industry
- Ability to navigate sophisticated HMI control systems on automated equipment
- Demonstrated ability to work effectively in a team
- Ability to work shifts to cover a 3-shift 5-day or 24/7 operation
- Strong verbal and written communication skills in English
- Basic computer skills
Preferred Qualifications
- Associate's Degree in a scientific discipline (or related field) and 2+ years relevant hands-on experience in a regulated production environment
- Knowledge of production equipment (e.g., spray dryers, product transfer equipment, isolator technology, filtration systems)
- Experience with process deviation investigations, CAPA, etc.
- Experience using test equipment (e.g., scales, balances, solids percentage testers, filter integrity testers)
Benefits
Eligible employees may participate in the Company’s comprehensive benefits suite, including medical/dental/vision/prescription coverage, employee wellness resources, savings plans (401k and ESPP), paid time off and paid parental leave benefits, disability benefits, and more.
Job Location
- On-site at the Durham, North Carolina location 100% of the time.
Pharmaceutical manufacturing professional with experience in upstream processes in a GMP environment. Handles raw materials, prepares and moves large-scale suspensions, and operates equipment such as tanks, mixers, and filtration systems. Maintains accuracy and compliance (weighing/dispensing materials and completing batch records), troubleshoots issues, collaborates on solutions, and takes process ownership to ensure upstream operations run seamlessly and support production of life-changing therapies.
Minimum Requirements
- H.S. Diploma or GED and 2+ years of relevant hands-on experience in a regulated production environment
- Strong cGMP documentation practices
- Experience with production equipment in a regulated industry
- Ability to navigate sophisticated HMI control systems on automated equipment
- Demonstrated ability to work effectively in a team
- Ability to work shifts to cover a 3-shift 5-day or 24/7 operation
- Strong verbal and written communication skills in English
- Basic computer skills
Preferred Qualifications
- Associate's Degree in a scientific discipline (or related field) and 2+ years relevant hands-on experience in a regulated production environment
- Knowledge of production equipment (e.g., spray dryers, product transfer equipment, isolator technology, filtration systems)
- Experience with process deviation investigations, CAPA, etc.
- Experience using test equipment (e.g., scales, balances, solids percentage testers, filter integrity testers)
Benefits
Eligible employees may participate in the Company’s comprehensive benefits suite, including medical/dental/vision/prescription coverage, employee wellness resources, savings plans (401k and ESPP), paid time off and paid parental leave benefits, disability benefits, and more.
Job Location
- On-site at the Durham, North Carolina location 100% of the time.