What are the responsibilities and job description for the MCS Manufacturing Associate NS position at BioPharma Consulting JAD Group?
We are seeking a Manufacturing Associate for the Night shift. In this role, you will be integral to supporting development, clinical, and launch activities within our cutting-edge manufacturing environment. Under general supervision, the Manufacturing Associate will perform operations as outlined in Standard Operating Procedures (SOPs) while adhering to Good Manufacturing Practices (GMP).
Key Responsibilities
Basic Qualifications
Key Responsibilities
- Execute hands-on operations including setup, cleaning, and sanitization of manufacturing equipment
- Prepare buffers and media in accordance with defined manufacturing procedures (MPs) and SOPs
- Strictly follow GMP documents (SOPs, MPs) ensuring safety and compliance
- Monitor critical processes and troubleshoot basic equipment issues as necessary
- Conduct in-process sampling and operate various analytical equipment
- Maintain a clean and organized workspace in compliance with safety standards
- Work in a cleanroom environment, utilizing personal protective equipment (PPE) appropriately
- Initiate quality reports and assist in drafting and revising SOPs and other essential documentation
- Identify and implement process improvements for increased efficiency
- Review documentation for compliance, including equipment logs and batch records
- Carry out physical tasks required for production operations including lifting, pushing, and standing for extended periods
- Strong mechanical aptitude and experience troubleshooting machinery
- Knowledge of GMP and regulatory requirements relevant to pharmaceutical manufacturing
- Familiarity with analytical techniques and lab practices associated with biopharmaceutical production
- Ability to engage in technical writing and documentation
- Proficiency in using process control systems
- Strong team player with the ability to communicate effectively with colleagues
- Able to work in a fast-paced environment with shifting priorities
Basic Qualifications
- Bachelor's degree OR
- Associate's degree and 4 years of experience OR
- High school diploma/GED and 6 years of experience
- Background in Biological Sciences or Engineering
- Prior experience in a regulated manufacturing environment
- Understanding of purification processes and biomanufacturing
