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Documentation Specialist - Fremont, United States - Aequor Inc
Description
Documentation Specialist III
Location: Fremont, CA/Remote
Duration: 6+ Months
The US Biopharma E&T (Engineering & Technology) Department is seeking a service partner to support revisions to our Facility and Engineering Drawings and Documentation database. These drawings are very critical to the site for design and maintenance activities. The drawings are maintained electronically in our CAD (Computer Aided Design) database. The department has a fluctuating amount of CAD work in support, driven by facility changes (CapEx projects), ranging from a few hours per week, to 40-60 hours at peak demand. Engaging an external partner with the necessary technical capabilities would allow the organization to address demand flexibly.
The business is located in Fremont, CA, and engages in the manufacture of biologic medicines, governed under FDA, EMA and other regulations.
Work Description
Perform requested updates to Engineering Drawings
Make changes to engineering drawings using AutoDesk AutoCAD or other drafting/modeling programs, to the specifications of the drawing project or redline documents.
Maintain drawings in the BI Engineering Drawing Management System (EDMS)
Download, upload, update, start/complete tasks and otherwise maintain drawings and data in the BI EDMS system. (Specifically, Siemens COMOS)
Maintains and Completes Work Orders in BI's task management system (MAXIMO)
Work Order tracking at BI is accomplished via the Maximo application and requires some manual input.
Complete requested work in a timely manner
Work will typically be expected to be completed within a regular schedule, but may include rushed/ time sensitive requests, which will require immediate attention and turnaround.
Maintain Open communication with BI Engineering Documentation
A weekly meeting may be conducted to assign workload to the service provider, as well as address task-related questions.
BI Intellectual property
Drawings may contain BI intellectual property and therefore must be treated as such. All BI files must be kept in a secure file system and may not be disseminated to unapproved individuals or organizations.
Requirements
Maintenance of a BI network account
Continuous on-time completion of all assigned training
Computing Equipment
Service provider must maintain one or more BI-issued personal computers
Collaboration
Service provider must collaborate within the confines of the BI communication channels only (e.g., BI email, MS Teams, Engineering Document Management System, etc.)
Works under minimal technical supervision from BI
Work location
The majority of the work is expected to be able to be performed remotely. On-site visits may be required on an ad-hoc basis, on same-day notice.
Task Management
Work tasks may be communicated at any time during the week
Work hours
Collaborative work must be performed in Pacific Time zone between the hours of 8am to 5pm
Service provider must be in proximity of the US Biopharma site in Fremont, CA
Ability to travel to site on same-day notice
Training
Vendor personnel furnished with a BI computer account and equipment must complete all assigned training in the BI LOS (Learning One Source system) by the due date for compliance.
Expert knowledge in AutoCAD and design
Site facility knowledge
Experience in GMP manufacturing facilities
An ability to read, understand and modify Engineering drawings, including P&ID's
Bachelor's Degree in Engineering
Three to five years of experience in related Life Science industry
Good knowledge and understanding of biopharmaceutical industry and AutoCAD experience
