Manufacturing Associate
Listed on 2026-09-12
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Manufacturing / Production
Pharmaceutical Manufacturing, Validation Engineer, Quality Engineering, Manufacturing & Industrial Operations
Pay Rate Low: 18.00 | Pay Rate High: 20.00
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: 18-20/hr.
If you are detail-oriented, eager to contribute to high-quality manufacturing processes, and excited about making an impact in the pharmaceutical industry
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.
- 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
- 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.
- Experience with equipment and cleaning validation.
- Proficiency in data analysis and visualization tools.
- Strong technical writing skills for documenting manufacturing processes and validation reports.
- 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.
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