Sr. Validation Engineer/Validation Specialist
Validation Technologies, Inc - San Diego, CA

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Direct-Hire/Full-Time

Strategic career opportunity to join a dynamic team of technical experts! Validation Technologies, Inc. ( VTI ) i s currently looking to identify several exceptionally talented Validation Engineering Professionals to complete our Biotech team in the greater San Diego, CA area. **Level/Title of position contingent on experience and expertise**

We are most interested in hiring motivated individuals who are excited about getting to the next level in their career with a desire to find a permanent "home" within our well-established global organization! These are high-impact and strategic roles within our successful company.

Validation Technologies, Inc. ( VTI ) strives to maintain and inspire professional excellence by providing Commissioning, Qualification, Automation, IT and Validation Services to the Pharmaceutical, Biotechnology, Biologics, Medical Devices and Lifesciences 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.

Responsibilities:
The Validation Engineer Will:
Join a dynamic CQV (commissioning, qualification and validation) team responsible for supporting, implementing, managing and executing high-profile Biotech/Biopharmaceutical capital projects
Have a passion for providing insight and direction pertaining to various validation and qualification activities on behalf of our organization
Have a desire to be a hands-on member of our high-caliber validation team responsible for writing, performing and executing IQ/OQ/PQ validation protocols/documentation for various activities related to validation/qualification in cGMP/FDA regulated environment; such as Process Validation, Cleaning Validation,Sterilization Validation, Equipment Validation, Equipment Qualification, Automation, Clean Utilities, Process Equipment, Purification, Temperature Mapping, etc.

Qualifications:
2-8 years of hands-on industry experience in cGMP/Biotech/FDA regulated industries
Bachelor’s degree or higher in Engineering, Life Sciences or related discipline (Engineering, Chemical Engineering, Chemistry, Biology, etc.), preferred
Recent and relevant experience related to one or more of the following (but not limited to):
Validation- Process Validation; Cleaning Validation; Sterilization Validation; Equipment Validation; Automation Validation; Critical Utility Systems; Temperature Mapping/ Kaye Validators/ Controlled Temperature Units/ Freezers/Data Loggers; Validation Master Plans (VMP); DeltaV, etc.

Qualification- IQ/OQ/PQ protocol development/writing/execution; Automation/Controls/G& Facilities; Utilities/HVAC; Process Equipment; Final Reports, etc.
Have working knowledge of cGMP/FDA regulations and experience in a biotech/ aseptic manufacturing environment
Proficiency in Microsoft Office including Word, Excel, PowerPoint, MS Project, Visio, 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
Must have strong ability to organize and manage multiple tasks in a fast-paced, but exciting environment

Validation Technologies Offers:
As one of the leading global Commissioning, Qualification, Automation, 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.

Validation Technologies, Inc - 12 months ago - save job - block