An established Biotech/Pharma firm based in the Greater Los Angeles area is currently seeking a driven Technical Writer with familiarity with cGMPs, SOPs and data migration activities. You will be working with a driven team that oversees their facilities as they make a transition to a new CMMS. They are looking to bring someone on to grow within their teams and seeking to start this with an initial 6 month contract with opportunity to hire.
- Write and revise documentation, SOPs, equipment specifications and checklists
-Responsible for the development of calibration and maintenance procedures for critical systems via an emphasis on risk assessment
-Collaborate with Quality Assurance and facilitate investigations related to mechanical or process deviation of equipment
-Read schematics and diagrams as well as protocols and other written materials
- Bachelor's Degree (Preferred) in engineering or sciences related field
- Familiarity with cGMPs, SOPs & documentation standards
- Minimum of 4 years of directly related experience with instrumentation, electrical systems, mechanical processes preferably in a pharma/biotech/medical device or other related field
-eagerness to collaborate and grow within a team
They are looking to bring someone on the team for an initial 6 months with a high possibility of converting to permanent depending on the quality of work! If you are interested in the Technical Writer role, then please don't wait to apply!