Formulation Technician II (3rd Shift)

Position Title: Formulation Technician II (3rd shift)
Work Location: Swiftwater PA 18370
Assignment Duration: 12 Months
Work Arrangement: Onsite
Shift Timings: 10PM to 6:30AM

Position Summary:
* The Formulation Department's role is to aseptically fill vaccines (syringes and vials). Included in this process is extensive preparation, cleaning rooms, cleaning equipment and material movement.
* The daily activities can include vial and syringe handling (wiping large boxes and moving large boxes), loading/unloading production supplies.

Background & Context:
This role supports vaccine manufacturing in a highly regulated aseptic environment following FDA guidelines.

Key Responsibilities:
* Aseptically fill vaccines (syringes and vials) including extensive preparation, cleaning rooms, cleaning equipment and material movement.
* Perform vial and syringe handling (wiping large boxes and moving large boxes), loading/unloading production supplies.
* Maintain extensive documentation while following strict Standard Operating Procedures (SOP's), Standard Work Instructions (SWI) and FDA guidelines.
* Maintain good housekeeping of work area and public spaces.
* Perform aseptic cleanings including preparation of disinfection solution, lifting 2-4 gallons of water, stretching to clean machines and ceilings while wearing additional PPE.
* Track own training and only perform tasks qualified for.
* Work safely, adhere to all personal protective equipment requirements, and follow reliability/flexibility expectations including possible overtime, weekends, and holidays.

Qualification & Experience:
* Lift a minimum of 30 pounds, and be able to push and pull a minimum of 50 pounds.
* Good reading and writing skills. Documentation is critical and a cGMP requirement.
* Ability to follow Standard Operating Procedures and Standard Work Instructions.
* Able to stand for long periods of time and perform all physical requirements including reaching, twisting, bending, squatting, and repetitive motion.
* Passing all exams and qualification tests (cGMP test and training modules).
* Basic computer skills.
* Must produce high quality work and work under tight deadlines while adhering to compliance rules and regulations.
* Able to work in an ever changing, semi-fast paced environment.