Validation Engineer
Millipore Corporation

Job Info

At MilliporeSigma, as one of our Validation Engineers working within a GMP/GLP contract pharmaceutical test environment, you will be providing validation support to operational departments per schedules and work requests. You will support site and departmental projects as required and coordinate with other support departments such as Facilities, Lab System Administrators, Calibration, and Safety. Key functions include: Implementation, periodic review, and revalidation of various Controlled Temperature Units and Analytical SystemsCompleting and maintaining Work Requests, Asset Records, and Schedules accurately and completely within the Asset Management SystemWorking to local and global validation and quality proceduresWorking alongside vendors and system owners on complex systems which include Computerized System Validation elements

Who you are:

Minimum Qualifications:

Bachelor's Degree in a scientific discipline (i.e. Biology, Chemistry, Biochemistry etc.) or engineering discipline (i.e. Computer Engineering, Information Technology Engineering, Mechanical Engineering, etc.), 1+ years' pharmaceutical industry experience or equipment and/or computerized system validation experienceORAssociates Degree in a scientific discipline (i.e. Biology, Chemistry, Biochemistry etc.) or engineering discipline (i.e. Computer Engineering, Information Technology Engineering, Mechanical Engineering, etc.)4+ years' experience in pharmaceutical industry

Preferred Qualifications:

Adaptable with a positive attitude who values customer support and learning new skillsTaking ownership while motivating key stakeholders to ensure project successExperienced with Microsoft Office programs (Word, Excel, Power Point, Teams) RSREMD