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Technical Writer

Newark Metro Area, NJ

Post Date: 08/07/2018 Job ID: JN -082018-22240 Job Type: Scientific
Essential Functions:

1) Technical Writing Responsibilities:
a. Draft, revise, review route and approve Standard Operating Procedures, Work Practices, Forms, and other type of GMP documentation deliverables.
b. Responsible for routing document deliverables through the Document Management system.
c. May assist with writing deviations, CAPAs, Change Controls.
d. Facilitate periodic reviews of SOPs.
2) Tracking Responsibilities
a. Keeps a log of documents and their states, including types, owner, reviewers, due dates, etc.
b. Follows up with team members and cross functional team members to encourage timely review and approval.
3) Promotes and provides excellent customer service and support
a. Regularly reviews, prioritizes and promptly responds to customer equipment maintenance, repair and support requests.
b. Provides technical support and guidance on calibration and maintenance issues. Interfaces with customers to ensure expectations are being met.
c. Maintains a positive relationship with all the members of the Equipment Commissioning & Qualification department and site customers while promoting a positive team environment.
4) Training and Compliance Wire Administration
a. Act as Department Administrator for Compliance Wire
b. Add, remove and update user information
c. Run monthly reports on user training status
5) Record Retention (RR)
a. Act as RR Notification Recipient for group
b. Ensure all department employees are trained on RR
c. Interface with all employees to ensure compliance to RR
d. Maintain accurate documentation of program completion
e. Maintain up to date RR binders

Microsoft Office Suite Word, Excel, PowerPoint and Outlook with extensive background in database systems. Basic user skills for Excel and PowerPoint are acceptable and they'll use Excel for tracking information. Innate ability to learn new software, such as corporate intranet and enterprise business.
Understands and works with all components related to web pages, i.e., web parts, lists, pages, libraries, permissions, content and forms
Strong working knowledge in computer training systems
Working knowledge of enterprise business systems such as Oracle or SAP preferred but not required.
Strong written and verbal communication skills. Highly proficient at writing well
formulated emails and notifications. Ability to effectively communicate with employees, contractors and vendors. Experience with technical writing and document development / generation.
Excellent interpersonal skills with experience dealing with a diverse workforce.
Strong multi
tasking ability in conjunction with proven organizational skills. Ability to organize assigned tasks in a high paced environment and concurrently monitor tasks / assignments with others that may impact timely completion. Ability to effectively manage multiple tasks and activities simultaneously
Familiarity with FDA and EU environments and associated compliance regulations


Professional Knowledge
Problem Solving
Team Player / Building Relationships
Customer Focus
Action and detail oriented
Active Listening

Education & Experience:

AA / AS degree or acceptable combination of education and practical experience
Minimum 5 years of Facilities/maintenance/engineering project coordinating / planning experience, preferably in a biotech environment.

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