Permanent Job Location: 91 Glenn Street, Lawrence, Massachusetts 01843.

POSITION DUTIES: Coordinate with the engineering group to carry out the design, automation, commissioning, and start-up of various processes, systems and facilities, including working in the full range of biotech/pharma project phase execution including all design phases, construction, startup, CQV, and project hand-over activities. Utilize engineering, vendor, and client specifications to generate and execute test protocols for process systems, process equipment and utility systems following client procedures and good documentation practices. Generate final and summary reports for executed test protocols. Provide technical and compliance input into project execution strategies to ensure regulatory requirements are met. Generate and support higher level project documentation as required such as masterplans, schedules, and summary reports.

Position requires Bachelor’s or foreign equivalent degree in Engineering field and a minimum of 5 years of experience in validation engineering in the biotech, pharmaceutical, or medical device industry, with experience to include writing and executing commissioning, verification, and validation protocols and reports, applying ASTM standards, utilizing manufacturing process equipment including CIP/COP systems, filtration skids, chromatography, fermentors, bioreactors, sterilization, and lyophilization equipment, testing equipment, and Kaye Validators and Dataloggers software.

How to Appy: Send resumes to HR, Attn: Kara Butterly, Trinity Consultants, Inc., 12700 Park Central Drive, Suite 600, Dallas, TX 75251.

Benefits: Trinity Consultants, Inc. offers competitive salary and benefit packages including medical, dental and vision coverage, 401(k) with employer matching, and other attractive incentives. Career development is encouraged through continuing education and participation in professional organizations.