Assistant Process Engineer

Integrated Resources, Inc ( IRI ) · Devens, Massachusetts

FULL TIME

Job Description

Description: 50% onsite required

Work Schedule: Mon-Fri (normal business hours)

The Senior Specialist, MS&T Validation provides process validation support to the Devens Cell Therapy Facility (CTF). The Senior Specialist participates in facility, process, and aseptic validation activities, including support of the Aseptic Process Simulation Program and implementation of process lifecycle management changes.

Job Responsibilities

Responsible for oversight of CTF Process Validation activities including, but not limited to Aseptic Process Simulations/ Validations (Client/APV), and other Lifecycle Management changes.

Prepares written protocols/reports/summaries supporting validation studies.

Ensures safe and compliant cGMP operations, maintains permanent inspection readiness.

This position reports to the Associate Director of Manufacturing Science and Technology Validation.

Specific Knowledge, Skills, Abilities

Experience in cGMP’s and multi-national biopharmaceutical/cell therapy regulations

Excellent verbal/written communication skills

Education/Experience/ Licenses/Certifications

Knowledge of science generally attained through studies resulting in a Bachelor’s degree in science, engineering, biochemistry or related discipline, is required

A minimum of 2 years’ experience in biopharmaceutical operations, or its equivalent is required.

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Company	Integrated Resources, Inc ( IRI )
Location	Devens, Massachusetts
Type	FULL TIME
Niche	Full-time

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Assistant Process Engineer

Job Description

This position reports to the Associate Director of Manufacturing Science and Technology Validation.Specific Knowledge, Skills, Abilities

This position reports to the Associate Director of Manufacturing Science and Technology Validation.

Specific Knowledge, Skills, Abilities