Currently I have an opening for a
Manufacturing Engineer located in
Frederick MD. Details for the position are as follows:
Job Description:- Complete required training to maintain technical skill, technical knowledge, and ensure compliance with cGMP requirements.
- Initiate deviation records in the Agile Quality Management System (QMS).
- Lead cross-function teams (Manufacturing, Quality, Facilities, MSAT, etc.) to perform root cause analysis of quality events.
- Collaborate with stakeholders to develop and manage Corrective and Preventive Actions (CAPA).
- Will perform technical writing, quality record management, owning and investigating deviations, implementing CAPAs, cell culture and aseptic processing
- Experience in cGMP or cell therapy manufacturing working with a Quality Management System (QMS).
- HS, Associates, or bachelor’s degree with relevant years of experience in GMP, Cell culture/upstream processing, and quality assurance.
Technical Information:- 12-month contract with the potential for extension or conversion to permanent
- $60-$68 hourly, depending on experience level
- Onsite, M-F, 8am-5pm
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Last updated on Oct 26, 2023