Specialist Manufacturing - Drug Development

GTT•Thousand Oaks, CA

8d•Onsite

About The Position

This role serves as an aseptic processing technical resource supporting 24/7 drug product manufacturing. The position will begin on a Monday–Friday, 8:00 AM – 5:00 PM schedule and transition to a Wednesday–Sunday, 8:00 AM – 5:00 PM schedule once 24/7 operations commence in 2027. The role is fully onsite.

Requirements

Drug product manufacturing experience
Aseptic compliance / contamination control knowledge
Outstanding communication skills
Doctorate degree; OR Master's degree and 2 years of experience; OR Bachelor's degree and 4 years of experience; OR Associate's degree and 8 years of experience; OR High school diploma / GED and 10 years of experience
Experience in drug product manufacturing (required — no drug product manufacturing experience is a disqualifying red flag)
Experience with aseptic compliance and/or contamination control in a manufacturing environment

Responsibilities

Support continuous improvement initiatives that strengthen aseptic compliance, process robustness, and operational efficiency.
Revise controlled documents, including SOPs, work instructions, and related records, to support process changes and improvements.
Own aseptic-related deviations.
Support the 24/7 Ways of Working Lead to evaluate 1 year of aseptic call log data from the floor and identify recurring trends, root causes, and improvement opportunities.
Develop clear metrics, summaries, and actionable outputs that convert operational data into decisions, priorities, and follow-up actions.
Establish and maintain a cyclic process for gathering information, addressing challenges, implementing improvements, and assessing effectiveness.
Provide on-the-floor support during aseptic operations.