JT578 - ASSOCIATE MANUFACTURING
- Completes work in accordance with established cGMP procedures and policies ( Standard Operating Procedures [SOPs], Manufacturing Procedures [MPs], Job Hazard Analysis [JHAs], Code of Federal Regulations [CFR]) with strict adherence to safety and compliance.
- Ensure proper gowning and aseptic techniques are always followed.
- Perform hands-on operation including set-up, cleaning, sanitization, monitoring of equipment and assigned area .
- Weigh and dispense of materials to be used in the preparation of Buffers and Medias.
- Complete washroom activities: cleaning equipment, small to large scale, use in production activities.
- Run and monitor critical process per assigned procedures.
- Perform documentation for assigned function (i.e., equipment logs, EBRs )
- Maintain an organized, clean, and workable space.
- High school diploma / GED + 1 year of manufacturing and/or other regulated experience
- Experience in a regulated industry such as biotechnology or pharmaceutical
- Basic understanding of GMP principles
- Strong verbal and written communication skills
- Proficient Microsoft Office skills
- Ability to follow detailed work instructions ( SOPs )
- Work Hours: 10-hours per day (Monday-Thursday or Tuesday -Friday).
- The schedule will transition to shifts (rotating 2-2-3, 12 hour shifts) upon completion of startup activities and as business needs dictate.
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
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