What are the responsibilities and job description for the Manufacturing QMS Specialist position at Global Life Science Hub?
Global Life Science Hub is excited to collaborate with an innovative biopharmaceutical company leading advancements in cutting-edge drug delivery technologies. Following two recent FDA approvals, they are gearing up for substantial growth. By 2025, they will launch new internal manufacturing facilities that will triple their production capacity as they seek their 3rd approval.
To support the next growth phase, we are seeking a Manufacturing QMS Specialist who will be responsible for writing and reviewing deviations, change controls, investigation reports, batch records, SOPs, CAPA etc. This position requires technical expertise in upstream and downstream process of biologics (Cytokines, monoclonal antibodies manufacturing)
Responsibilities:
Global Life Science Hub is a specialized Life Science headhunting firm. We place professionals across the United States and Europe for various Biotechnology, Pharmaceutical, and CDMO companies, ranging from small start-ups to large global organizations.
If you're interested, please apply below. If this position doesn't suit you, visit our website for more vacancies - www.glshub.com
To support the next growth phase, we are seeking a Manufacturing QMS Specialist who will be responsible for writing and reviewing deviations, change controls, investigation reports, batch records, SOPs, CAPA etc. This position requires technical expertise in upstream and downstream process of biologics (Cytokines, monoclonal antibodies manufacturing)
Responsibilities:
- Responsible to support manufacturing team with all kinds of documentation
- Documentation includes reviewing executed batch records (both Upstream department and Downstream batch record)
- Responsible for filing change controls, deviation, CAPA for manufacturing department
- For all critical / major investigation, will have to use investigation tools like 5why or 6M method
- Attend daily meetings with both upstream and downstream process to get all the documentation requirement for the day
- Meet weekly with QA to avoid any delay in the QMS closure
- Author batch records, SOPs and associated forms / formats required for manufacturing process
- Responsible for requesting / submitting all GMP documents to QA
- Support manufacturing process during critical campaign
- 10% wet lab work
- Performs other functions as required or assigned
- Complies with all company policies and standards
- A Minimum BA or BS in Biological Sciences or related technical field is required
- At least 3 years of experience in Biopharmaceuticals
- Knowledge in USP and DSP process
- Experience working with Biologics is strongly preferred
Global Life Science Hub is a specialized Life Science headhunting firm. We place professionals across the United States and Europe for various Biotechnology, Pharmaceutical, and CDMO companies, ranging from small start-ups to large global organizations.
If you're interested, please apply below. If this position doesn't suit you, visit our website for more vacancies - www.glshub.com
