Industry X – MES Pharmasuite Specialist
| Company | Accenture |
|---|---|
| Location | Boston, MA, USA, Seattle, WA, USA, Houston, TX, USA, Des Moines, IA, USA, Nashville, TN, USA, San Francisco, CA, USA, Austin, TX, USA, Detroit, MI, USA, Cleveland, OH, USA, Bentonville, AR, USA, Los Angeles, CA, USA, Tampa, FL, USA, Livingston, NJ, USA, Miami, FL, USA, Dallas, TX, USA, Raleigh, NC, USA, Philadelphia, PA, USA, Chicago, IL, USA, Charlotte, NC, USA, St. Louis, MO, USA, Arlington, VA, USA, Milwaukee, WI, USA, Carmel, IN, USA, Beaverton, OR, USA, Pittsburgh, PA, USA, Sacramento, CA, USA, Walnut Creek, CA, USA, Albany, NY, USA, Scottsdale, AZ, USA, Columbus, OH, USA, Hartford, CT, USA, Oklahoma City, OK, USA, New York, NY, USA, Minneapolis, MN, USA, Denver, CO, USA, Mountain View, CA, USA, Atlanta, GA, USA, San Diego, CA, USA, St. Petersburg, FL, USA, Cincinnati, OH, USA, Overland Park, KS, USA |
| Salary | $28.41 – $94.23 |
| Type | Full-Time |
| Degrees | Bachelor’s |
| Experience Level | Junior, Mid Level |
Requirements
- A minimum of 1 year of experience with Rockwell FactoryTalk PharmaSuite (FTPS) MES solutions in a highly automated Life Sciences manufacturing environment
- Bachelor’s Degree or equivalent (minimum 3 years work experience). If Associate’s Degree, must have equivalent minimum 6 years work experience
Responsibilities
- Lead in the design, development, documentation, and implementation of Manufacturing Execution Systems (MES)
- Design/Author/Develop/Configure Electronic Batch Records (EBR)
- Implement MES solutions and integrate with ERP and control equipment
- Documentation of MES configuration and validation of EBRs
- Provide organization oversight for complex systems involving the development of MES
- Work closely with business management and users to strategically define the needs and design solutions that add value
- Partner with business clients and delivery teams to determine appropriate solutions
- Direct the activities of team in the above tasks
- Document and analyze the information needs of the business and ensure appropriate solutions are delivered
- Gather user requirements in relation to controlling and recording manufacturing activities
- Respond to requests for client proposals
- Manage and develop client relationships
- Global System Implementation
- Manage medium-small teams and/or projects
Preferred Qualifications
- Knowledge of FDA and GMP guidelines
- Understanding of Life Sciences validation processes
- Working knowledge of software Development Life Cycle (SDLC) and support methodologies
- Strong written and oral communication skills
- Ability to work in a team-oriented, collaborative environment
- Ability to facilitate meetings and follow up with resulting action items