Current Opportunities at A&J include:

VALIDATION ENGINEER

REFERENCE ID: AJVE2010-1

DUTIES: Evaluate and analyze various manufacturing processes. Design equipment and develop processes for manufacturing, utilizing principles and technology of chemistry and engineering. Conduct research to develop new and improved manufacturing processes. Prepare piping & instrumentation diagrams (P&IDS), feasibility reports to carry chemical processes. Analyze operating procedures and equipment and machinery functions to reduce time and cost. Generate validation documents for equipment, utilities, cleaning and process. Develop development study protocols. Coordinate resources to support project activities. Develop and maintain procedures, specifications and drawings. Develop standard operating procedures in compliance with current good manufacturing practices (CGMPS) and applicable FDA and EU guidelines. Prepare Site Validation Master Plans. Develop GAP Analysis Reports to harmonize overall operational and qualification procedures. Please include the Reference ID on your application/resume.

REQUIREMENTS: Master’s degree or its equivalent in Pharmaceutical Engineering or Chemical Engineering

HOURS: Monday through Friday 9:00am To 5:00pm

LOCATION: A&J Consulting Engineering Services, 164 Brighton Road, Clifton, NJ 07012

Interested candidates must Fax their resumes to: (973) 777.5528