Title: Quality Control Technician I
Location: Swiftwater, PA
Duration: 12 Months+ Possible Extension
Schedule: M-F 8:00am-4:30pm EST- 1st Shift
Pay Range: $24- $26/hr
Manager Note: The candidate must pass an eye exam and receive vaccinations to be eligible for this position.
Description:

• This position supports the execution of routine testing in the Quality Control Microbiology laboratory while strictly adhering to site work instructions, Federal Regulations, cGMP, and Client policies and procedures.
• This position requires the individual to perform routine testing as scheduled to support production, method validation as well as the stability program, and completing the required documentation.

Job Responsibilities:

• Knowledge of general Microbiological techniques including aseptic processing and culturing of both bacterial and viral isolates.
• Activities include assisting with maintaining safety and compliance of the laboratory work area; Performing cleaning of laboratories, equipment, and ancillary areas as required.
• Attending/Contributing to scheduled team meetings, department, and safety meetings.
• This position requires proficiency and understanding of the theory related to processes, assays, and equipment as well as the ability to identify issues/trends.
• Develop a working knowledge of appropriate compendia and/or regulatory guidance.
• Participation in various and assigned phases of Quality Control testing
• Duties may include (but are not limited to): Visual Evaluation of vials, syringes, plates, bottles, and canisters.
• Setup and breakdown of equipment.
• Documentation, waste disposal, cleaning of laboratories, and all other activities as assigned.
• The candidate must pass an eye exam and receive vaccinations to be eligible for this position.

Requirements:

• Bachelor’s Degree in Microbiology or Biological Sciences with 1-2 years of experience.
• Prior Quality Control experiences are desirable.
• Knowledge of microbiological techniques and experience with tissue culture, sterility, or bioburden is preferred.
• Exceptional attention to detail and strong writing skills are crucial.
• The individual must be familiar with cGMP guidelines.
• The candidate must be able to work in a team environment.