Process Control Shift Supervisor

THE RITEDOSE CORPORATION•Columbia, SC

1d•Onsite

About The Position

The Process Control Shift Supervisor will be responsible for the execution and completion of tasks performed by the PC Inspectors. The Process Control Shift Supervisor will manage the PC Inspectors to ensure the proper inspection and documentation of filling and/or packaging, line clearance, fill volume checks, and physical inspections of bulk and finished product. Also responsible for all training required of the PC Inspector position.

Requirements

A minimum of three years’ experience in regulated manufacturing industry preferably within Process Control or a similar Quality Department.
High School Diploma or GED
Ability to handle multiple priorities; lead and participate in daily operational activities
Ability to work flexible work schedules
Ability to manage multiple tasks concurrently
Ability to establish, prioritize and implement tasks with minimal supervision
Ability to lead others to accomplish company and departmental goals and objectives
Strong oral and written communication skills
Ability to lead and develop a team-oriented working relationship within the operation

Nice To Haves

Leadership experience also preferred.

Responsibilities

Coordinate vacation and shift coverage for special projects for the PC Inspectors on the shift.
Continuous review of proper batch record documentation of all inspection activities performed within the shift.
Coordinate PC Inspector activities on shift to support production efficiency.
Communicate and coordinate interdepartmentally as needed to ensure schedule adherence.
Point of contact for deviations or atypical events.
Coordinate and correct actions and returning the line to production.
Review/approve inspections in LIMS and release product in ERP system.
Conduct, investigate, and/or assist the PC Manager with investigations, incidents, deviations, and completion of required stability testing.
Support and assist with PC Inspector duties as demand and scheduling dictate.
Assist with Freeweigh system administration for new users or troubleshooting user /password issues.
Review of lab documentation for accuracy and adherence to cGMP documentation standards.
Provide feedback to Management for continuous improvement efforts within the department.
Follow Standard Operating Procedures, safety, health, and cGMP Guidelines.