Development Service Technician

The Development Service Technician will be responsible for the disassembly, cleaning, and storing process equipment. The Development Service Technician will collaborate with the Manufacturing team and scientists for any urgent cleaning needs - rooms and equipment.

About the role

• Understanding specific cleaning agents used to clean equipment and manufacturing suites.
• Cleaning of equipment per specific details in Work Instructions.
• Absolutely ensure all cleaning activities are documented in equipment and room logbooks, accurately and compliant with SOPs and FDA cGMP guidelines.
• Disassembly of dirty equipment before and during cleaning.
• Assembly of cleaned equipment parts, per Work Instructions.
• Aid with setups and changeovers with adherence to SOPs and safety requirements.
• Attendance at morning Tier meeting to understand and follow up on daily room and equipment cleaning needs.
• All other duties as assigned.

Responsibilities

• Understand specific cleaning agents used to clean equipment and manufacturing suites.
• Clean equipment per specific details in Work Instructions.
• Absolutely ensure all cleaning activities are documented in equipment and room logbooks, accurately and compliant with SOPs and FDA cGMP guidelines.
• Disassemble dirty equipment before and during cleaning.
• Assemble cleaned equipment parts, per Work Instructions.
• Aid with setups and changeovers with adherence to SOPs and safety requirements.
• Attend morning Tier meeting to understand and follow up on daily room and equipment cleaning needs.
• Perform all other duties as assigned.

Requirements

• High school diploma or equivalent.
• At least 1 year of manufacturing experience or completion of Grads2Work Program or BioWorks certificate program.
• Ability to lift 50 lbs unassisted, and push and pull in excess of 100 lbs.
• Majority of work day is performed while standing and walking.
• Requires the use of hands for simple grasping and fine manipulations.
• Occasionally bend, stoop, twist, and have full range of motion in upper and lower extremities.
• Exposure to hazardous chemicals, other active chemical ingredients, dust, fumes, gases, skin and respiratory irritants, moving machinery parts, and damp, humid and wet environments.
• Must be able to use a variety of tools, equipment, and machinery.
• Employment is contingent upon being able to complete a medical evaluation with satisfactory results.

Qualifications

• High school diploma or equivalent.
• At least 1 year of manufacturing experience or completion of Grads2Work Program or BioWorks certificate program.
• Ability to lift 50 lbs unassisted, and push and pull in excess of 100 lbs.
• Majority of work day is performed while standing and walking.
• Requires the use of hands for simple grasping and fine manipulations.
• Occasionally bend, stoop, twist, and have full range of motion in upper and lower extremities.
• Exposure to hazardous chemicals, other active chemical ingredients, dust, fumes, gases, skin and respiratory irritants, moving machinery parts, and damp, humid and wet environments.
• Must be able to use a variety of tools, equipment, and machinery.
• Employment is contingent upon being able to complete a medical evaluation with satisfactory results.

Skills

• Understanding specific cleaning agents used to clean equipment and manufacturing suites.
• Cleaning of equipment per specific details in Work Instructions.
• Documenting cleaning activities in equipment and room logbooks.
• Disassembly of dirty equipment.
• Assembly of cleaned equipment parts.
• Aiding with setups and changeovers.
• Attendance at morning Tier meetings.

Benefits

• Competitive medical benefits and 401K.
• 152 hours of PTO + 8 Paid Holidays.
• Dynamic, fast-paced work environment.
• Opportunity to work on Continuous Improvement Processes.

Pay

• Details about pay are not specified in the job posting.

Schedule

• Shift: Monday - Friday 3 pm - 11:30 pm.

Company Information

Catalent’s Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development.