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Tuesday, November 2, 2010

Andover, MA - Sr. Process Validation Engineer

Job Description:
  • Provide engineering technical support related to installation, startup/commissioning, testing, and qualification of new process equipment and process related systems
  • The engineering contractor would support ongoing operations and projects at the Andover facility
  • Job requirements will involve process equipment system design, development and execution of startup documents and commissioning plans, troubleshooting of equipment, development and execution of the qualification activities, assisting maintenance, attending necessary meetings and training sessions
  • NO OVERTIME OR TRAVEL REQUIRED
  • AT THIS TIME, THE COMPANY DOES NOT FORESEE THESES ASSIGNMENTS GOING BEYOND JUNE 2011
  • IDEAL EDUCATION BACKGROUND TO BE IN MECHANICAL AND/OR CHEMICAL ENGINEERING
REQUIREMENTS:
  • MOST CRITICAL: EXPERIENCE IN A SIMILAR FACILITY; MECHANICAL DESIGN SKILLS; AUTOMATION EXPERIENCE; GMP BACKGROUND
  • Candidate should have a BS/MS in chemical or mechanical engineering or relevant discipline
  • Candidates must have a minimum of 5-10 years of experience with biopharmaceutical process systems executing design, commissioning, troubleshooting, and qualification activities
  • They must have a working knowledge of cGMP type systems and practices
  • Computer skills, ability to work across functional areas such as operations and maintenance are required to provide appropriate support
  • MS Office: Application Knowledge Required 4-7 years Advanced
  • Architecture or Facilities Management: Business Skills/Knowledge Required 4-7 years Advanced
  • Chemical: Industry Knowledge Required 4-7 years Advanced
  • Biopharmaceutical: Industry Knowledge Required 4-7 years Advanced
  • Good communication skills and written skills are needed
  • Availability to work off-shift as needed
SUBMIT RESUME to Resume@ABOUT-Consulting.com
Please Include Job Title and Location in the Subject Line of Your Email

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