Supply Chain Technical Writer II

About the role

Join a top-tier global pharma leader in Branchburg, NJ, as a Supply Chain Technical Writer II. This 6-month extendable contract role offers an excellent opportunity to drive manufacturing excellence, facilitate CAPA closures, and streamline critical GMP documentation within a dynamic supply chain environment. Position located in Somerville, New Jersey. Contract type, 9 am–5 pm work hours, bachelor’s degree required.

Responsibilities

• Partner with Supply Chain SMEs to author, revise, and manage GMP documentation, including SOPs, work instructions, specifications, and Change Controls.
• Facilitate CAPA closures and actively participate in Operations-related process improvement initiatives.
• Develop standardized document formatting and content structures to ensure logical organization while minimizing gaps and duplication.
• Collaborate with Quality and Supply Chain teams to ensure all documentation meets or exceeds compliance expectations.
• Compile supporting change management documentation and follow up with reviewers and approvers to meet project timelines.

Qualifications

Required:

• Bachelor's degree in a scientific discipline or 5+ years of equivalent experience.
• 3-6 years of relevant experience in a pharmaceutical manufacturing environment.
• Demonstrated experience authoring and revising GMP documentation and managing change controls.
• Proficiency in Microsoft Office applications (Word, Excel, Access, PowerPoint).

Preferred:

• Experience with advanced document management applications and process improvement techniques.
• Strong cross-functional communication and meeting facilitation skills.

Skills

• SOP Development
• Good Manufacturing Practices (GMP)
• Corrective and Preventive Actions (CAPA)
• Clinical Supply Chain Risk Mitigation

Benefits

Randstad offers a comprehensive benefits package, including medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

Schedule

Standard work hours: 9 am to 5 pm.