FUJIFILM Diosynth Biotechnologies · 2 days ago
QA Specialist, LMS
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BiotechnologyHealth Care
Insider Connection @FUJIFILM Diosynth Biotechnologies
Responsibilities
Performs administrative side of ComplianceWire (serve as Administrator)
Updates Learning Management Systems and processes to address general questions regarding learning techniques
Assigns training to users, performs quarterly audit of training system to ensure training is aligned with role and curricula
Assists with continual development of education program
Collaborates alongside team to work with Area Management/Leadership to define training needs, goals and ensure they align with company
Collaborates alongside team to develop overall training metrics
Collaborates with other Fujifilm Diosynth Biotechnologies sites to gain alignment and efficiency
Other duties, as assigned
Qualification
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Required
High School Diploma or GED with 6 years’ experience in a cGMP manufacturing operation and/or Quality oversight, in an FDA regulated facility OR
Bachelor’s degree with 2 years’ experience in a cGMP manufacturing operation and/or Quality oversight, in an FDA regulated facility OR
Master’s degree with no previous cGMP experience
Learning Management Software (LMS) experience
Proficient in MS Office suite
Preferred
2-3 years’ experience cGMP manufacturing operation facility
Experience on at least 1 – 2 greenfield projects
Experience with training content creation (SOPs, eLearnings, Classroom training, OJTs)
MasterControl experience
ComplianceWire Administrator experience
Working knowledge of Smartsheet software
Training and/or familiarity with Quality Risk Management principles
Experience delivering training and information relating to education program
Company
FUJIFILM Diosynth Biotechnologies
Fujifilm Diosynth Biotechn, contract development & manufacturing provider for preclinical, clinical and commercial biologics manufacturing.
Funding
Current Stage
Late StageLeadership Team
Recent News
Wake County Government (.gov)
2024-05-24
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