Manufacturing Technician - cGMP Ops & Process Improvement

Clutch Canada; United States; On-site; USD 42,000 - 64,000; Full time

Job summary

Liquidia is seeking a hands-on Manufacturing Technician in Morrisville, NC, onsite. The role supports production and R&D by running manufacturing equipment, providing feedback to engineering and scientific staff on process performance, and contributing to process improvement.

Ideal candidates have a strong documentation skill set, mechanical aptitude, and experience in a cGMP manufacturing setting, with flexibility for first and second shifts.

Qualifications

• B.S. degree with 0-2 years of manufacturing operations experience, Associate's degree with 2-5 years, or 5-8 years of manufacturing experience.
• Hands-on experience in operation of manufacturing equipment or instrumentation.
• Strong mechanical aptitude with proven record of equipment troubleshooting and upkeep.
• Experience with fluid coatings, UV curable materials, printing or related technologies a plus.
• Ability to work cross-functionally with Quality Assurance, Quality Control, Engineering, Maintenance, and other support groups.

Responsibilities

• Follow SOPs and Master Batch Records while running manufacturing equipment to support commercial manufacturing schedule.
• Support in troubleshooting equipment issues, and investigations for deviations and CAPAs.
• Document all production activities in appropriate room and equipment logbooks.
• Interact cross-functionally with Quality Assurance, Quality Control, Engineering, Maintenance, and other support groups.
• Maintain detailed laboratory notebooks and preparation of batch records.
• Adhere to GLP and GMP guidelines as required to maintain a compliant, safe and clean work environment.

Skills

Documentation

Technical skills

Troubleshooting

Education

B.S. degree

Associate's degree

Job description

Liquidia is seeking a hands-on Manufacturing Technician in Morrisville, NC, onsite. The role supports production and R&D by running manufacturing equipment, providing feedback to engineering and scientific staff on process performance, and contributing to process improvement.

Ideal candidates have a strong documentation skill set, mechanical aptitude, and experience in a cGMP manufacturing setting, with flexibility for first and second shifts.