Manufacturing Supervisor

Agilent Technologies

About The Position

The Manufacturing Supervisor establishes functional business plans and technical project objectives to meet the production organization's short- and long-term goals. In this role, you will be leading employees and/or production departments responsible for manufacturing oligonucleotides and API, and design/ implementation of production area processes. This also entails directing and handling resources to implement tactical plans and department programs/projects for business.

Requirements

Bachelor’s or Master’s Degree or equivalent plus directly relevant experience
1+ years of experience as a manager, supervisor and/or lead individual contributor in an FDA regulated GMP facility; 2+ years will be helpful
Demonstrated leadership in a chemical/manufacturing production environment
Experience drafting, reviewing, and completing SOP's, Change Controls, Non-Conformance Records, CAPA's and KPI's
Demonstrated ability to lead and drive the execution of processes, projects, and tactical initiatives
Emergency Response Team training and participation strongly preferred

Nice To Haves

2+ years of CDMO experience a plus
CQV experience a plus

Responsibilities

Develops and implements solutions to department issues, coordinates day-to-day manufacturing operations, and ensures all SOPs, safety procedures, and administrative tasks are performed on time and accurately by all direct reports.
Works closely with Manufacturing Manager to increase safety, quality and efficiency by making and tracking metrics and leading cross-department initiatives to drive site improvements.
Consistently demonstrates and upholds Agilent Core Values.
Understands Agilent's overall mission and be able to deliver that message and results.
Provide guidance and mentorship
Work in cross-functional teams for continuous site improvement, and assist in interviewing, hiring and onboarding process for the Manufacturing department