(CW) Training Associate (TEMPORARY) at BioMarin. Hybrid role based in Novato; onsite 2 days per week (Tuesdays or Wednesdays plus another on-site day).
Responsibilities
Administration of the Learning Management System (LMS) to ensure seamless customer experience for users in BioMarin manufacturing and manufacturing support groups
Provision of training reports in support of audit and inspection
Leading or assisting department projects as needed
LMS Administrative Requests: Building training curricula in association with the customer department/group
Supporting project on migrating to paperless credit system
Processing of training assignment requests, including curricula and user group creation and modification
Processing node structure changes and the associated re-grouping of personnel
Entering training record data for non-LMS driven activities
Integrating multiple types of e-Learning training modules into the LMS
Creation, editing and archive of documentation as directed by department management
Creation and delivery of custom reports as requested
Maintain and update training database
Participate in internal and external audits and inspections
Review documents (SOPs) and TNAs, provide feedback on the contents, and assess training needs for new and revised procedures
Supporting department logistics as needed
Deliver training as applicable
Interact with customers across manufacturing and support groups to address technical support inquiries
Train on administrator tools on ad-hoc and planned basis
Guide/educate customers in the design of curricula and their implementation in the LMS to maximize efficiency and consistency
Support department logistics as needed
Identify and recommend process improvements
Lead or support improvement projects for training systems or programs
Qualifications
Required: Administration of the LMS (ComplianceWire, Veeva, SAP etc.)
Required: Application of data integrity best practices in a corporate environment
Required: Use of web-based database software applications
Required: Effective customer service across all levels of business
Preferred: 2-4 years in a regulated environment supporting highly technical processes
Preferred: 4-6 years of experience in professional training
Preferred: Excellent written and verbal communication skills
Preferred: Ability to comprehend technical information related to equipment, process and regulatory expectations
Preferred: Familiarity with Biotech, Pharmaceutical and/or Medical Device Industry
Preferred: Microsoft Office Suite β Excel, Outlook, SharePoint, Visio, Word
Education
Bachelorβs Degree in technical discipline preferred (biological sciences preferred, but not required)