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Engineer II

Job

NewAgeSys Inc

West Point, PA (In Person)

Full-Time

Posted 4 days ago (Updated 2 days ago) • Actively hiring

Expires 7/23/2026

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Job Description

Req#
MSD1JP00003249
Req Number:
MSD1JP00003249
Req Title:
Engineer II
Client:
A Major Pharma Company
Work Address:
West Point, PA
Req Release Date:
06/18/2026
Duration:
12 months Hours a week: 40 Hours Position Summary
Responsibilities:
Supports deviations, including assessment of product impact and determination of root cause and corrective/preventative actions, assists in writing of investigations as well as quality incidents. Authors, supports, updates, and/or leads documentation updates such as SOPs, batch records, change control documents, technical protocols, validation documents and other GMP documentation. Supports equipment and facility projects for the Sterile Supply areas. Supports continuous improvement projects that increase compliance, reduce cost, and/or simplify/standardize the process. Examines complex issues from diverse perspectives (safety, compliance, automation, equipment, process, and people) to best understand and resolve the root cause. Designs, conducts, and/or reviews and approves experimental protocols as needed. Provides on-the-floor support of complex operational and technical (process/equipment) issues. Completes and/or leads projects to improve the performance of our Company processes, including investigation and execution of Corrective/Preventative Actions (CAPAs); projects aimed at improving Right-First-Time performance or preventing/reducing deviations; and projects that seek to improve efficiency, reduce cost, or increase compliance. Supports team safety, environmental, and compliance objectives. Manages project timelines to ensure key compliance and customer due dates are met; escalates any potential delays and develop remediation plans when possible. Partners effectively with Operations, Quality, Planning, project teams, Automation, Maintenance, and external vendors.
Qualifications:
Education:
B.S. or B.A. in Engineering, Sciences, or related discipline. 2-4 yrs experience (combination of co-op/Real world acceptable).
Required Experience and Skills:
Strong Technical Writing Skills, Highly developed communication, leadership and teamwork skills. Ability to manage projects/work to schedule/deadlines.
Preferred Experience and Skills:
Deviation Management Investigation. Experience in biologics, vaccine, or bulk sterile manufacturing facilities. Change Control experience. Experience in root cause analysis. Experience in manufacturing environment. Ability to meet quick pace/hard deadlines. Any previous SAP and/or Power BI experience beneficial