Process Validation Engineer

Please send the resumes to careers@starkassociatesllc.com or

Contact: +1 848-300-0022

Job Title: Process Validation Engineer

Location: Rahway, NJ

Duration: Long Term

Responsibilities

• The automation process engineer will be responsible for day-to-day operations support activities, in a GMP environment, including but not limited to the following technologies:

• Delta V DCS, Siemens PLC, Allen Bradly PLC and other related technologies.

• Responsibilities include troubleshooting issues, identifying trends, process monitoring, system administration, update documentation, querying data, operator training and participating in deviation investigations.

• Must be able to communicate clearly (oral and in writing) and frequently with operations and other support groups.

• Engineers are also expected to provide off-site weekend/evening automation phone or on-site support.

• Candidate will also be responsible for designing, implementing, testing, and closing-out change controls for automation related corrective actions and continuous improvement initiatives.

• Education Minimum Requirement:

• Bachelor Degree in Engineering, Computer Science, Electrical, Chemical, Mechanical or equivalent with 2+ years of relevant experience within pharmaceutical industry.

• Knowledge of cGMP’s and multi-national biopharmaceutical regulations.

• Possess strong verbal/written communication skills.

• Ability to think strategically and to translate strategy into actions