Manufacturing Technician (2nd Shift)

Kindeva Drug Delivery•Lexington, KY
•Onsite

About The Position

Kindeva Drug Delivery is hiring a Manufacturing Technician to support the manufacture of prescription nasal spray medications at its Lexington facility. The role involves operating and monitoring manufacturing equipment and processes, preparing equipment and production rooms, maintaining accurate GMP documentation, supporting team training and validation activities, and helping maintain and improve manufacturing operations. The position is on-site and scheduled for second shift, 3:00 PM–1:30 AM, Monday through Thursday and every other Friday. The work environment may involve exposure to highly potent chemical compounds, hazardous materials, and toxic or controlled substances. Employees must comply with PPE requirements, safe work methods, site safety procedures, and established practices that protect personnel and product quality.

Requirements

  • High school diploma or GED.
  • Previous experience in a GMP-regulated manufacturing environment.
  • Ability to follow SOPs and accurately complete GMP manufacturing documentation, including batch records and logbooks.
  • Strong communication and interpersonal skills and ability to work effectively in a team environment.
  • Ability to meet applicable requirements for working with controlled substances.
  • Regularly handle materials and supplies, use computers for extended periods, communicate by telephone and electronically, and stand and walk for extended periods.
  • Occasionally lift and/or move up to 25 pounds and use proper lifting techniques.
  • Adequate vision to read and execute documentation and perform job tasks compliantly and safely.
  • Remain aware of workplace hazards and follow site safety procedures.
  • Adhere to stringent PPE requirements and established safe work methods in an environment with potential exposure to highly potent chemical compounds, hazardous materials, and toxic or controlled substances.

Nice To Haves

  • Pharmaceutical manufacturing experience.
  • Experience with sterilization processes or aseptic techniques.

Responsibilities

  • Follow batch records to operate, monitor, and control equipment and process parameters during manufacturing.
  • Complete training and follow Standard Operating Procedures (SOPs) to clean, sanitize, and prepare process equipment and production rooms for manufacturing.
  • Accurately complete required Good Manufacturing Practice (GMP) documentation.
  • Maintain assigned manufacturing areas in accordance with 5S principles.
  • Assist with training and onboarding other manufacturing team members.
  • Assist with execution of validation protocols for manufacturing and support equipment.
  • Participate in routine preventive maintenance on facilities and equipment.
  • Identify and escalate equipment or process issues affecting manufacturing operations.
  • Recommend manufacturing process or facility improvements and cost-saving opportunities.
  • Perform other duties as assigned by management.
  • Follow site safety procedures and required PPE and safe-work practices.
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