Formulation Technician II (12hr days or 12hr nights; 2-2-3 rotation schedule)

Thermo Fisher Scientific•Greenville, NC
•Onsite

About The Position

As part of Thermo Fisher Scientific, the Formulation Technician II helps produce sterile injectable pharmaceutical products and addresses moderate-scale problems using analysis and critical thinking. The role follows written and verbal instructions to manufacture products in accordance with industry guidelines and regulations. It is based in Greenville, North Carolina, in the DPD division, with full-time day or night shifts from 6 a.m. to 6 p.m. or 6 p.m. to 6 a.m. on a 2-2-3 rotating schedule. The position involves working in an aseptic filling area and performing manufacturing activities such as cleaning, line changeovers, parts preparation, filter integrity testing, operation of parts washers, autoclaves and a filling isolator, tray loading and unloading, and material handling. The technician also troubleshoots equipment alarms and records production activities in batch records, logbooks and controlled forms. Work is conducted in a cleanroom and requires gowning and personal protective equipment. The environment may include cold rooms and freezers, changing hot and cold temperatures, loud equipment, and hazardous or toxic materials.

Requirements

  • High school diploma or equivalent.
  • At least 1 year of work experience in manufacturing, operations, production, a laboratory setting or a related field.
  • Ability to work effectively in a team, follow standard operating procedures and perform repetitive duties.
  • Basic math skills.
  • Good verbal and written communication skills.
  • Attention to detail while maintaining product quality.
  • Ability to meet the physical and environmental requirements, including lifting, standing and moving about, and wearing required gowning and personal protective equipment.

Nice To Haves

  • Experience in a cGMP environment.

Responsibilities

  • Manufacture pharmaceutical products in accordance with area SOPs and current cGMP requirements.
  • Verify and document production activities in batch records, logbooks and controlled forms.
  • Perform tasks in an aseptic filling area, including cleaning cGMP areas, line changeovers, parts preparation, filter integrity testing, tray loading and unloading, and material handling.
  • Operate parts washers, autoclaves and the filling isolator.
  • Troubleshoot equipment alarms.
  • Follow written and verbal instructions and applicable safety and quality requirements.
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