
MES (Manufacturing Execution System) Engineer
- Philadelphia, PA
- Permanent
- Full-time
- Perform general engineering tasks related to MES, as delegated by the system owner (IT Manager), such as Recipe Authoring, Equipment Tracking configuration, administration-level configuration updates, report configuration (Crystal Reports), data mining (SQL query authoring), etc.
- Assist team with operational activities (e.g. end-user support, break-fix) for all aspects of MES system (Electronic Batch Record/Recipe Authoring, Equipment Tracking/Workflows, Order/Inventory Management, interface to external systems/instruments, etc.) - on-call support required.
- Act as technical resource for major MES projects (EBR authoring and deployment)
- Knowledge of pharmaceutical business processes, Part 11 data integrity, infrastructure, architecture, and technology to support business supporting manufacturing.
- Partner with business teams, learn business processes and drive continuous improvement initiatives to provide operational efficiencies and cost reductions.
- Must adhere to Iovance Biotherapeutics' core values, policies, procedures, and business ethics.
- Perform miscellaneous duties as assigned.
- Travel requirements less than 10%
- On-site at Philadelphia manufacturing facility
- 2-4 years of hands-on experience and exposure working in biotech/pharma information technology and/or consulting for the pharmaceutical industry.
- A minimum of 1 year of experience performing Recipe Authoring within Emerson Syncade MES.
- Bachelor's degree required, preferably in Computer Science, Engineering, Chemical/Biomedical Engineering, or similar field of study
- Experience in pharmaceutical and/or medical device industries.
- Strong understanding of CRF 21 Part 11, Annex 11, cGMP, GAMP5
- Experience implementing and administering MES (Emerson Syncade)
- Familiarity with the back-end design, operation and the supporting database structure of Syncade MES is a plus.
- Experience configuring interfaces between MES and external systems (ERP, LIMS, BMRAM, etc) and instruments (cell counters, scales, etc) is a plus
- Experience with Iovance's additional systems including ERP (NetSuite), Building Management and Environmental Monitoring (Siemens Desigo), LIMS (Labvantage) and CMMS (Blue Mountain) is a plus.
- Experience with Computer System Validation (CSV) is highly preferred.
- Experience with cell and gene therapy/biologics manufacturing preferred.
- Strong interpersonal, presentation and communication skills.
- Possesses sense of urgency; identifies challenges and problems and takes the initiative to identify solutions.
- Can work as an effective team resource as well as independently.
- Must be able to remain in a stationary position standing or sitting for prolonged periods of time.
- Must be able to move about inside an office and exert up to 10 pounds of force occasionally or a negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects.
- Must have visual acuity to perform activities such as: preparing and analyzing data and figures, viewing a computer screen, and extensive reading.
- This position requires repetitive motion, substantial movements (motions) of the wrist, hands, and/or fingers.
- Must be able to communicate with others to exchange information.