Task Description
The incumbent is extremely detailed oriented with exceptional paperwork abilities. The incumbent will end up being skilled and proficient at a lot of or all system operations in their location, frequently leading the execution of treatments, and carries out most functions with very little guidance.
- Performs production processing actions and/or making assistance activities, keeping track of the procedure versus the batch record and control system. Might coordinate or lead procedure actions as asked for
- Documents/Records and Evaluations cGMP information and details (consisting of paperwork of variances) for processing actions and/or devices activities, following standard procedure. Modifies or produces files as advised. Secret paperwork consists of batch records, SLRs, and devices logbooks.
- Actively takes part in training activities, handling their specific training strategy. Trains other partners as needed.
- Performs recognition procedures with very little supervision/direction of others.
Credentials
- High School Diploma or comparable
- Targeted biopharmaceutical training (Bioworks or comparable) and/or associated basic training likewise chosen.
- Comprehensive oriented with exceptional paperwork abilities
- Runs in a safe way in order to prevent injury to self and others
- Strong peer and group management abilities.
- Versatile to altering requirements and needs, comfy browsing in an altering environment
- Comfy with uncertainty; rapidly comprehends the requirements based upon the circumstance at hand
- Affecting and leading a favorable mindset throughout group
- Capability to interact plainly and efficiently to all levels of the company
- Capability to communicate with others in an expert and polite way in accordance with Biogen’s Core Behaviors
- Capable to work a 12-hour shift, both day shift or graveyard shift
Extra Info
The Production Partner carries out and records everyday production operations in a cGMP environment that includes operation of procedure devices, execution of recognition procedures, developing/ modifying cGMP files and other tasks.
