Our client, a renowned leader in biotechnology, is revolutionizing the use of living cells to create groundbreaking biologic medicines. As a guiding force in the biotech industry, they set the bar for innovation and advancement.

We are seeking a Manufacturing Associate to join our dynamic team and support GMP drug substance manufacturing and validation activities. This individual will play a crucial role in manufacturing operations, ensuring compliance with industry standards while contributing to process optimization and data analysis.

Location: Raleigh/Apex, NC
Contract to Hire
Pay: 19-21/hr.

Key Responsibilities

• Execute manufacturing operations and support activities on the production floor.
• Perform GMP and non-GMP production runs (small- and large-scale).
• Handle material preparation, equipment setup, and cleaning validation in compliance with GMP guidelines.
• Assist in process validation and technical support for manufacturing activities.
• Collect and analyze data related to manufacturing performance and validation.
• Support documentation processes, including batch records and deviation reports.
• Collaborate with cross-functional teams (Engineering, Process Development, and Quality Assurance) to optimize manufacturing workflows.
• Contribute to continuous improvement efforts and best practices in drug substance manufacturing.

Education & Experience Options:

• High School Diploma/GED + 4 years of relevant work experience
• Associate’s Degree + 2 years of relevant work experience
• Bachelor’s Degree + 6 months of relevant work experience

Required Skills:

• Hands-on experience in GMP technical support, validation, engineering, or process development.
• Knowledge of drug substance manufacturing processes.
• Exposure to project management and process improvement initiatives.

Preferred Skills:

• Experience with equipment and cleaning validation.
• Proficiency in data analysis and visualization tools.
• Strong technical writing skills for documenting manufacturing processes and validation reports.

Why Join Us?
🌟 Opportunity to work on cutting-edge drug manufacturing processes.
🌟 Hands-on experience in a regulated GMP environment.
🌟 Collaborative, growth-focused team with opportunities for career advancement.

If you are detail-oriented, eager to contribute to high-quality manufacturing processes, and excited about making an impact in the pharmaceutical industry, we encourage you to apply!

**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**

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