Process Development Technician - II
Position Summary
We are seeking a Process Development Technician to support manufacturing and laboratory process development for a leading global pharmaceutical company.
In this role, you will work alongside engineers and scientists to develop, test, optimize, and validate manufacturing processes while ensuring compliance with quality, safety, and regulatory standards.
This is an excellent opportunity for someone with hands-on manufacturing or laboratory experience who enjoys troubleshooting equipment, analyzing process data, and contributing to continuous process improvements in a regulated environment.
Schedule: 3rd shift Monday-Friday 8pm-4:30am
Key Responsibilities
Support the development, optimization, and scale-up of manufacturing and laboratory processes.
Operate, calibrate, troubleshoot, and maintain process equipment and instrumentation.
Collect, analyze, and document process data to evaluate performance and identify improvement opportunities.
Develop and maintain Standard Operating Procedures (SOPs) and process documentation.
Assist with equipment and process validation activities, including IQ, OQ, and PQ protocols.
Collaborate with engineering, manufacturing, quality, and laboratory teams to achieve project goals and timelines.
Ensure compliance with GMP, safety, environmental, and quality standards.
Train operators and technicians on new or updated manufacturing processes and procedures.
Participate in continuous improvement initiatives to enhance process efficiency and reliability.
Qualifications
Required
0-4 years of experience in process development, manufacturing, laboratory support, or a related technical environment.
Strong mechanical aptitude and hands-on troubleshooting skills.
Experience operating and maintaining manufacturing or laboratory equipment.
Ability to interpret technical drawings, schematics, and process documentation.
Experience collecting and analyzing process data.
Strong problem-solving skills and attention to detail.
Excellent communication and teamwork abilities.
Preferred
Associate degree in Engineering Technology, Industrial Science, Manufacturing Technology, or a related technical field.
Experience working in a GMP, ISO, or other regulated manufacturing environment.
Familiarity with process validation activities (IQ/OQ/PQ).
Knowledge of Lean Manufacturing or continuous improvement methodologies is a plus.
Why Join This Opportunity?
Gain experience supporting projects at a world-renowned pharmaceutical company.
Work with experienced engineers and scientists on innovative manufacturing processes.
Build valuable experience in process development, validation, and regulated manufacturing.
Competitive hourly pay with overtime eligibility.