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Actalent Technical Writer in Bedford, Massachusetts

If interested, please apply and send your resume to marcmill@actalentservices.com

Top Skills' Details:

Technical Writing

cGMP

OOS Investigations

Root Cause Analysis

Product Quality Complaints

SOP

Description:

Collaborate with manufacturing, plant services, engineering to ensure timely documentation, root cause analysis, and QA closure of Stage II OOS investigations and OOT investigations

• Work directly on technical investigations relating to product quality complaints

• Participate in other quality investigations and risk assessments as requested to perform review of documents, processes, testing, etc.

• Author/revise standard operating procedures (SOPs) and batch records, as required

Additional Skills & Qualifications:

2- 4 years of pharmaceutical manufacturing experience

Familiarity with regulatory/compliance environment

Knowledge of cGMPs

Experience with manufacture of radiopharmaceuticals preferred

About Actalent:

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

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