Senior Validation Engineers Job

Job Duties: Responsible for validation execution and documentation. Review and approve vendor validation protocols for technical accuracy and compliance. Execute validation protocols, write validation reports, and prepare validation protocols where applicable. Responsible for utility and equipment qualification execution, and represent QA role in utility, equipment, process and assay validation planning and execution. Participate in software validation as required. Interact with functional departments to ensure compliance in validation activities, and interface with contractors in validation activities. Other duties & responsibilities as determined by management. The position reports to the Sr. QC Manager and is ideally suited for a professional with extensive technical knowledge, and a proven track record of developing and carrying out validation processes.

Requirements: Minimum of a Bachelor’s in Molecular Biology, Biochemistry, Microbiology, mechanical engineering, or related life science field plus minimum three (3) years experience as Validation Engineer, Validation Consultant, Quality Consultant, or closely related in biopharmaceutical or biologics industry. Specific Experience: Three (3) years hands on experience in facility, utility, equipment, instrument validation. Must be familiar with GMP operational principles and documentation as evidenced by three (3) years of experience. Must be able to work independently, be self-motivated, and results oriented, as evidenced by three (3) years of experience.

Job Offer in Pennington, NJ for ProBio Inc. Send cover letter, CV, salary requirements and references to ProBio, Attn: HR-1, 311 Pennington Rocky Hill Rd., Bldg 9, Pennington, NJ 27560