Technical Writer - Scientific-I

ID# DCNJ30616

dinaliC is an international consulting firm specialized in projects for numerous industries. We are dedicated to provide contract and permanent opportunities for skilled professionals in their area or areas of expertise


The Technical Writer will be responsible for supporting the Quality Operations function by processing change orders for controlled document, process and equipment validation and qualification activities according to established standards and company procedures. 

Key responsibilities include, but are not limited to: Processes changes for new documents, process changes and introduction of new laboratory equipment. Responsible for coordinating commissioning activities of new laboratory equipment. Follows company procedure to safely decommission obsolete laboratory equipments. 

Reviews change documents for accuracy and consistency with other documents. Analyzes controlled documents for inconsistencies, gaps or errors to drive process quality improvement and compliance with company SOPs. Provides support to validation and qualification projects. Technical Writer is responsible of re-engineering documents to meet current specifications and good documentation practices. Responsible for creating controlled documents for new laboratory equipments. Demonstrates ability to use GMP ‘good documentation practices’. Technical writer identifies and updates affected documents prior to obsolete a controlled document. 

Supports process improvement activities. Verifies change implementation and closure of completed change orders. Processes validation and verification protocols and reports for laboratory equipments as necessary, while company established guidelines and procedures. Creates and Submits IT self services. Responsible for developing and delivering awareness training to associates. 

Daily responsibilities: Writing change order for controlled documents. Defining the change plans to implement change orders. Defining changes and description for documents. Meets with supervisor to give updates on changes in process. Negotiates content of changes with users, and implements changes using electronic documentation system.

Position Details:

Medical Device


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