JT783 – ASSOCIATE MANUFACTURING NS
Holly Springs, North Carolina, United States
Job Description
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:
Qualifications:
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.
Responsibilities:
- 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.
- Buffer and Media preparation and transfer. 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.
Qualifications:
- High school diploma / GED + 1 year of manufacturing and/or other regulated experience OR Associate's degree
- 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)
- Initial schedule will be Monday-Thursday or Tuesday -Friday, 10 hours days.
- 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.
Apply
Career Focus: Manufacturing
This role is part of a curated selection of life science opportunities featured on Xtalks. Employers may request edits or removal here.
Similar Jobs
Manufacturing Operations Associate – Union...
Overview Who we are: Dendreon is making the battle against cancer person...
Manufacturing Technician I/II/III
Life changing therapies. Global impact. Bridge to thousands of biopharma...
AFB International – Manufacturing Technician...
This opportunity is located within our AFB International business, the g...
Manufacturing Technician
About Neuralink: We are creating devices that enable a bi-directional in...