Sr. Specialist Cell Therapy
- Category: Manufacturing
- Deadline: 01st March 20232023-03-01T00:00:00-0800
- Massachusetts
SR. SPECIALIST CELL THERAPY DEVENS, MA 100% Onsite. Required Skills:
- Bachelor's degree in a related field from an accredited college or university required.
- Minimum of 3 years relevant work experience required, preferably in the pharmaceutical, biotechnology, or cell therapy manufacturing industry.
- Strong project management and/or change management skills are helpful.
- Minimum of 1 year of experience with project coordination and cross-functional team leadership preferred.
- Minimum of 1 year of experience with the execution of electronic batch records required, experience supporting electronic batch record creation and testing preferred, preferably Syncade MES.
- Knowledge of Delta V or other process automation software desirable.
- Ability to use process historian and analyze data to assist troubleshooting.
- Computer System Validation (CSV) experience creating/running test scripts helpful but not required.
- Apply manufacturing process expertise and electronic batch record technical knowledge to own electronic batch record changes and the associated change controls.
- Own Electronic Batch Record (MES/Syncade) Functional specifications. Ensure consistent execution of recipe modifications and changes. Ensure adherence with governing documents related to change management.
- Works collaboratively with Manufacturing, Digital Plant, IT, Validation, Quality, and MS&T to ensure change initiatives are driven to closure and migrated to the production area in a timely manner.
- Owns the lifecycle of an electronic batch record change .
- Works with site functional teams, including manufacturing, engineering, warehouse, and quality assurance to gather user requirements for recipe development.
- Understanding of MES library objects. Use that understanding to direct changes to MES recipes and/or directly update the MES recipes utilized in Manufacturing.
- Develop documentation to support the qualification of the MES recipes, including test scripts and functional specifications.
- Execute testing of the recipes in the development environment to ensure functionality.
- Manage User Acceptance Testing process for recipe qualification.
- Provide technical support by troubleshooting and resolving MES issues to support manufacturing operations.
- Develop and deliver reports from reporting software.
- Able to use creative problem solving.
- Provides technical expertise to management and less experienced professionals.
- Perform other tasks as assigned.
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