Sr. Manufacturing Technician - 2nd Shift

Liquidia Corporation; Morrisville (NC); On-site; USD 42,000 - 66,000; Full time

Benefits offered by this job

Medical

Dental

Vision

STD

LTD

401(k)

ESPP

Job summary

Liquidia Corporation is seeking a hands-on Manufacturing Technician to operate and monitor manufacturing equipment, support production and R&D, and provide feedback for process improvements. The role emphasizes adherence to SOPs, Master Batch Records, and cGMP standards, while collaborating with engineering, QA, QC, and maintenance to ensure safe, high-quality production.

The ideal candidate will bring strong documentation, troubleshooting skills, and the ability to balance multiple tasks in a

Qualifications

• The candidate should be highly detail-oriented with excellent documentation skills.
• Strong troubleshooting abilities and mechanical aptitude.
• Ability to work in a cGMP/GLP manufacturing environment.
• Ability to collaborate cross-functionally with QA, engineering, and maintenance.

Responsibilities

• Follow SOPs and Master Batch Records while running manufacturing equipment to support commercial scheduling.
• Troubleshoot equipment issues and investigate deviations and CAPAs.
• Document all production activities in appropriate room and equipment logbooks.
• Multitask and adapt to changing priorities.
• Interact cross-functionally with QA, QC, Engineering, Maintenance, and other support groups.
• Maintain focus on safety, quality, and cGMP compliance.
• Participate in training activities and manage own training plan.
• Collect samples for in-process testing and complete test and inspection activities.
• Monitor the manufacturing process, record run parameters, and adjust as necessary within the process window.
• Support manufacturing runs including material handling, inventory management, equipment cleaning, and scheduling.
• Apply hands-on process development experience and equipment upkeep to support operations.
• Support manufacturing operations in sample preparation and testing.
• Maintain detailed laboratory notebooks and batch records.
• Perform experiments with guidance from engineering and scientific staff.
• Adhere to GLP and GMP guidelines to maintain a compliant, safe, and clean environment.
• All other duties as assigned.

Job description

Liquidia is deeply passionate and committed to the discovery, engineering, and development required to bring novel therapies to patients who need them most, and to the healthcare providers who care for them. Our current drive is toward improving the treatment of pulmonary hypertension (PH). We will continue to combine our proprietary, innovative PRINT® Technology with new and established medications, offering the potential for both better precision and improved clinical outcomes. Our team members include some of the industry’s top scientists, clinicians, business strategists, engineers, and pharmaceutical executives. We work together to help people lead longer, healthier, and happier lives.

Job Summary

We are looking for a hands-on and experienced Manufacturing Technician. In this role, you will perform routine running of manufacturing equipment to support production and R&D efforts. Furthermore, you will provide feedback to engineering and scientific staff on process performance and ideas for process improvement.

Job Responsibilities

• Responsible for following SOP’s and Master Batch Records while running manufacturing equipment to support commercial manufacturing schedule
• Support in troubleshooting equipment issues, and investigations for deviations and CAPA’s
• Document all production activities in appropriate room and equipment logbooks
• Flexibility to multitask and adjust to varying priorities.
• Interact cross functionally with Quality Assurance, Quality Control, Engineering, Maintenance, and other support groups.
• Attention to detail with focus on safety, quality, and cGMP’s
• Actively participates in training activities, and managing their own training plan.
• Collect samples for in-process testing and complete test and inspection activities
• Monitor the manufacturing process, recording observations and key run parameters as needed, and adjusting the process as necessary within the defined process window
• Provide support to manufacturing runs including material handling, inventory management, equipment cleaning and scheduling of routine runs
• Apply hands-on experience with process development, equipment upkeep, and troubleshooting
• Apply hands‑on experience to support manufacturing operations in sample preparation and testing
• Maintain detailed laboratory notebooks and preparation of batch records
• Perform experimentation with guidance from the engineering and scientific staff
• Adhere to GLP and GMP guidelines as required to maintain a compliant, safe and clean work environment.
• All other duties as assigned

Job Requirements

• The desired candidate should be highly detailed with exceptional documentation skills, technical skills, and troubleshooting skills.
• The candidate should also be able to work in a cGMP commercial manufacturing operations.
• 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 as part of a cross functional team with manufacturing, research and development, analytical and biology staff
• B.S. degree with 0‑2 year’s of manufacturing operations experience, Associate’s degree with 2‑5 years’ manufacturing experience, or 5‑8 years of manufacturing experience.
• Must be willing to work first and second shift

Liquidia offers a competitive compensation package as well as a comprehensive benefits package that includes Medical, Dental, Vision, STD, LTD, 401(k) Savings Retirement Plan, ESPP, and more!

Liquidia is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Reasonable accommodation may be made to enable qualified individuals with disabilities to perform the essential functions of this position.