As part of the initial startup team, you’ll play a key role in commissioning, qualifying, and validating new equipment and systems
Job Summary
As part of the initial startup team, you’ll play a key role in commissioning, qualifying, and validating new equipment and systems.
This role offers a unique opportunity to help establish the foundation of a world-class manufacturing operation and contribute to building and training future team members.
We value employees who can quickly learn on the job, proactively anticipate and resolve manufacturing or delivery challenges, and consistently uphold the highest standards of quality.
Matching Summary
As part of the initial startup team, you’ll play a key role in commissioning, qualifying, and validating new equipment and systems.
Salary
Base: $39.65 - $61.96/hr; Bonus/Equity: eligibility for bonus, stock; Benefits: eligibility for benefits
Skills & Requirements
Must-have
GMP-regulated environment
commissioning, qualification, and validation
operate and maintain lab instruments
write and revise SOPs
troubleshoot critical process equipment
Nice-to-have
proactively anticipate and resolve challenges
thrives in dynamic environments
building and training future team members
familiarity with oligonucleotide synthesis
Key Requirements
Associate's or Bachelor’s degree in scientific or technical field, or equivalent experience
4+ years of experience in pharmaceutical or GMP manufacturing
Experience in chemical processing facility/PSM regulated environments/ clean room environments, or FDA-regulated manufacturing highly desired