Technical Writer

TechDigital Group; Summit (NJ); On-site; USD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a Supply Chain Specialist to drive investigations and improve compliance in their operations. This role involves collaborating with various departments to ensure business requirements are met and developing training materials for the Infinity System. The ideal candidate will have a background in pharmaceutical manufacturing, with strong technical writing skills and experience in project coordination. Join a dynamic team where your contributions will enhance operational efficiency and compliance, making a significant impact in a fast-paced environment.

Qualifications

• 2 years of relevant work experience in pharmaceutical manufacturing preferred.
• Experience in project coordination and technical writing is a plus.

Responsibilities

• Drive investigation of deviations in Supply Chain by collaborating with peers.
• Develop and maintain technical training material for Infinity System.

Skills

Technical Writing

Project Coordination

Cross-Functional Team Leadership

Supply Chain Management

Quality Assurance

Education

Bachelor's Degree in a Related Field

Job description

Responsibilities

1. Drive investigation of Deviations in Supply Chain by collaborating with peers and internal customers (e.g., Manufacturing, Quality Control, Quality Assurance, IT, Warehouse, and Manufacturing Shared Services).
2. Translate and/or write technical business requirements which are compliant, efficient, and effective in QMS.
3. Coordinate meetings and presentations with leadership/peers and internal customers to ensure business requirements are met for any Supply Chain activities.
4. Develop and maintain technical training material and provide training to users for Infinity System in Supply Chain/Warehouse.
5. Collaborate with Scheduling, ERP, Warehouse and other Supply Chain functions to continuously improve and find effective ways to maintain compliance through work practice, standard operating procedures and work instructions.
6. Understand manufacturing processes and the implementation within the Quality systems at site.

Skills and Experience

1. Bachelor's degree in a related field from an accredited college or university preferred.
2. An equivalent combination of education, experience and training may substitute.
3. 2 years relevant work experience required, preferably in a pharmaceutical manufacturing environment including technical writing or Quality/Supply Chain role.
4. A year of experience with project coordination and cross-functional team leadership preferred.