High Value Production Operator

West Pharmaceutical Services•Kinston, NC

1d•Onsite

About The Position

To work as a team member to process High Value Products (HVP) through the HVP process with minimal assistance from management or engineering. Team members must have the ability to work with other team members in a cell concept rotating through multiple job functions throughout the day, following a playbook for optimal performance. Team members must be able to perform job functions with a full gown/goggles in which no skin is visible within the area for multiple hours at a time. Ideal candidates are quick thinking and confident to ensure consistent processing and foresight to know the next task required. It is the responsibility of this individual to ensure that product/customer specifications are followed always. Ideal candidates have previous cGMP experience and have the knowledge of how to operate within a classified clean room.

Requirements

High School Diploma or GED required.
No minimum experience required.

Nice To Haves

2+ years in cGMP environment or relevant work experience preferred.
Preferred candidate will have experience working in or processing in a controlled clean room and have knowledge of cGMP requirements for controlled environments.
Must possess an acute attention to detail and be willing and able to work in a team environment.
Make good decisions within authorized job responsibilities.

Responsibilities

Strictly adhere to all requirements pertaining to gowning for entry into classified clean room areas.
Candidates must be able to pass gowning qualifications to enter classified clean rooms.
Accurately maintain all required documentation and paperwork to ensure lot traceability.
Operate pharma wash equipment and oversee processes within classified clean rooms such as pre-staging, staging, loading, unloading and final packaging, per cGMP standards.
Strict adherence to product/customer specifications.
Ensure that weight/count equipment is set up accurately and within calibration.
Correctly sample product for QA inspections and pre-delivery samples in cGMP manner.
Keep equipment and work area in clean and orderly condition.
Operate Envision system correctly according to all applicable procedures.
Operate steam sterilization process including but not limited to start functions such as loading, unloading and packaging.
Input and log data correctly for the Autoclave process when needed.
Perform all positive pressure and cleaning requirements for all classified cleanrooms associated with the HVP Processing department.
Alert the Area Manager to conditions that may prevent meeting production and quality expectations.
Operate PC, printers and scanners as required.
Performs other duties as assigned based on business needs.
Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.

Benefits

Generous Paid Time Off (PTO)
Flexible vacation, personal, and holiday leave
Opportunities for professional growth through training programs
Tuition assistance
Leadership development
Skill-certification initiatives
Performance-based bonuses
Service recognition
Employee appreciation initiatives
Volunteer opportunities through West without Borders initiative and other charitable programs