US Citizen and Green Card and a contract role

Need to be flexible with the shifts AM to PM

Description:

Typical Day:

These responsibilities include some of the following:

* Demonstrate company Values – Patient Focus, Transparency, Respect, and Integrity – in every interaction, in every work task, and with every responsibility of the job role.

* Live company's Expectations of Courage, Accountability, Development, and Teamwork to achieve high performing behaviors in the workplace.

* With good documentation and data integrity practices, safely and compliantly completes and documents daily manufacturing tasks per standard operating procedures, batch document instructions, and logbooks.

* Proactively work with senior staff to achieve competency in production operations.

* Supports in cross-functional activities, such as engineering actions, validation actions and Tech Transfer actions, including proactive safety and compliance input prior to execution.

* Primarily these activities are within the production suite but sometimes require out-of-suite or off-site work (i.e. FAT support).

* Monitors equipment and critical process parameters and escalate any issues or abnormalities and participating in the resulting troubleshooting activities.

* Strives to maintain a high level of competency with current and emerging digital platforms (SAP, EBR, AR/VR, etc).

* By learning the production schedule and assessing it daily, proactively ensures all processing equipment and necessary materials are adequate and available to set the team up for success.

· Transparently participates in investigations that are the result of safety or compliance issues.

Education Requirements:

• BS/BA degree, with cGMP manufacturing experience.

• OR an Associate’s degree from Montgomery county community college in Biotechnology or related technical field with cGMP manufacturing experience.

• OR High School degree, 1+ years of cGMP manufacturing experience.

• Open to any other scientific background education or experience.