Location: Greater Phoenix, Arizona
Extraordinary opportunity to join a dynamic team of technical experts! Validation Technologies, Inc. ( VTI ) is currently looking to identify several exceptional Senior-Level Validation Engineers to complete our Biopharma team in the greater Phoenix, Arizona area. **Level/Title of position contingent on experience and expertise**
These are high-impact and strategic roles within our global organization. One in which a great deal of success will be determined by the Sr. Packaging Validation Engineer/Project Manager's ability to lead and execute our high-profile validation projects for some of the most prestigious Biopharmaceutical organizations in the world!
Validation Technologies, Inc. ( VTI ) strives to maintain and inspire professional excellence by providing Commissioning, Qualification, IT and Validation Services to the Pharmaceutical, Biotechnology, Biologics and Medical Devices Industries. VTI offers professional development, training, competitive compensation, excellent benefits, 401K plus a stimulating and collaborative work environment. We are committed to providing exciting career opportunities in a work environment that values trust, respect, openness, teamwork, creative talent, enthusiasm and diligence.
The Senior Validation Engineer/Project Manager Will:
Join a dynamic Validation team responsible for supporting, implementing, managing and executing high-profile Biopharmaceutical validation projects
Have a passion for providing expertise and direction pertaining to various validation and qualification activities on behalf of entire VTI organization
Have desire to be hands-on key member of high-caliber Validation team responsible for validating (IQ, OQ, PQ, and PV) 3 fill/packaging lines and packaging equipment
The level, compensation and title of position will be contingent on one’s level of experience and expertise
2-15+ years of relevant industry experience in cGMP/Biotech/Pharmaceutical/FDA regulated industries
Bachelor’s degree or higher in Engineering, Life Sciences or related discipline
Recent and relevant experience related to the validation/qualification of one or more of the following : Pharmaceutical packaging processes; Packaging Equipment; Fill Line/Filling; Packaging Lines; Process Validation; Validation Master Plans (VMP); Protocol execution; IQ, OQ, PQ, PV (IOQ) protocol development; Final reports, etc.
Have working knowledge of cGMP/FDA regulations
Proficiency in Microsoft Office including Word, Excel, PowerPoint, MS Project, etc.
Strong interpersonal and communication aptitude, coupled with a high propensity for attention to detail as well as self-motivated initiative
Exceptional technical writing, review and analytical skills in addition to strong verbal communication and presentation skills
Validation Technologies Offers:
As one of the leading global Commissioning, Qualification, IT and Validation Services organizations, VTI is always looking for innovative, talented and experienced technical professionals for our multinational and global offices. We offer some of the best salary and benefit packages in the industry for our full-time/permanent employees as well as competitive hourly pay for our contractors.