Industry X-MES PAS-X Consultant
| 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, Miami, FL, USA, Morristown, NJ, USA, Irvine, CA, USA, Dallas, TX, USA, Raleigh, NC, USA, Redmond, WA, 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, Kirkland, WA, USA, Albany, NY, USA, Reston, VA, 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 2 years of experience with Körber PAS-X 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 Körber PAS-X 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
- Work closely with business management and users to strategically define the needs and design solutions that add value
- Document and analyze the information needs of the business and ensure appropriate solutions are delivered according to GxP standards
- Respond to requests for client proposals
- Manage and develop client relationships
Preferred Qualifications
- Knowledge of FDA and GMP guidelines
- 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
- Understanding of Life Sciences validation processes
- Working knowledge of software Development Life Cycle (SDLC) and support methodologies