Manufacturing Associate

Our client, a renowned leader in biotechnology, is adding a Manufacturing Associate to their team in Wake County, NC! This role is responsible for supporting the manufacturing cleaning validation team in carrying out cleaning and sterilization validation tasks.

Shift: 8 am-5 pm (Mon-Fri)

Pay: Starting at $18/hr

Type: 12-month contract (possibility of extension or conversion)

Responsibilities

• Develop validation protocols and reports related to cleaning and sterilization validation.
• Ensure timely review and closure of executed cleaning validation protocols.
• Prepare necessary solutions to support validation activities (e.g., riboflavin).
• Support the manufacturing cleaning validation process by ensuring protocol samples are collected and tested within the required timeframe.
• Create and update GMP manufacturing documents, including SOPs, FORMS, and protocols.
  
  

Requirements

• High school diploma or GED with 4 years of experience in GMP Technical Support, Validation, GMP operations, Engineering, or Process Development.
• Technical knowledge of drug substance manufacturing and a comprehensive understanding of related support functions.
• Experience in project management or project support.
• Preferred experience in equipment and cleaning validation.
• Strong data analysis and/or data visualization skills.
• Experience in technical writing.
  
  

This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

INDBH