Title: Manufacturing Associate
Location: Oklahoma City, OK
Shift: 1st or 3rd | Mon-Fri
Rate: $24-25/hr.+ benefits
We are currently recruiting for multiple Manufacturing Associates for a contract development and manufacturing organization (CDMO) specializing in the production of biologics, particularly for the early-stage development of new drugs.
Job Responsibilities:
- GMP Manufacturing: Executing and monitoring cell culture-based processes, ensuring compliance with GMP guidelines.
- Cell Culture Techniques: Performing routine tasks like media preparation, cell inoculation, and bioreactor operation.
- Quality Assurance: Collaborating with QC and QA teams to maintain product quality and regulatory compliance.
- Troubleshooting: Identifying and resolving process deviations.
- Documentation: Maintaining accurate and complete batch records.
- Technology Transfer: Contributing to process improvement initiatives.
- Training: Assisting in training junior team members and developing SOPs.
- Safety: Maintaining a clean and organized work environment and following safety protocols.
Job Requirements/Qualifications:
- Bachelor's degree in a relevant scientific field.
- 2-5 years of experience in GMP manufacturing, with a focus on cell culture.
- Knowledge of bioreactor operations, aseptic techniques, and upstream processing.
- Familiarity with regulatory requirements (FDA, EMA).
- Problem-solving and analytical skills.
- Effective communication and teamwork.
- Attention to detail and documentation.
Additional Job Details:
- Competitive Salary and Benefits Package
- Overall, the Manufacturing Associate position requires a highly skilled individual with a strong background in cell culture and GMP manufacturing.
- The role involves a combination of technical expertise, problem-solving skills, and a commitment to quality and compliance.
- M-F; Flexible to work day or night shift
