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Job Description

A Life Science company based in San Diego, CA is seeking a Principal Technical Project Manager to join their team. Leads cross-functional teams to address business systems needs/issues. Plans and directs the analysis of complex business problems to be solved with automated systems. Provides technical leadership in identifying, recommending and evaluating systems and procedures that are cost-effective and meet user requirements. Plans and leads unit integration and acceptance testing; and may create specifications for systems to meet business requirements. Provides consultation to users in the area of automated systems.

We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to Human Resources Request Form (https://airtable.com/app21VjYyxLDIX0ez/shrOg4IQS1J6dRiMo) . The EEOC "Know Your Rights" Poster is available here (https://www.eeoc.gov/sites/default/files/2023-06/22-088\_EEOC\_KnowYourRights6.12ScreenRdr.pdf) .

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Skills and Requirements

Bachelors Degree in computer science, IT or related field and 8+ years of relevant experience OR masters degree in computer science, IT or related field and 6+ years of relevant experience

Project Management Certification highly preferred

8+ years of Technical Project management experience (working in a pharmaceutical company with exposure to FDA regulations preferred)

Experience managing technical implementation projects in support of business applications

Experience with cloud-based softwares/platforms (Veeva, ServiceNow, NetSuite)

o Familiarity of Veeva and its support functions including: clinical, quality, safety& regulatory

Experience with ERP

Experience with Microsoft applications technologies such as MS SQL Server, Oracle, JAVA, Visual Basic, MS Access, MS Project, IIS, Internet Explorer, and

Experience with Advanced Web technologies such as HTML, XML, SGML, Dynamic HTML, JavaScript, VBScript, and Internet Database Programming.

Experience supporting validated systems/validation applications for regulatory purposes in a biotech/pharmaceutical company.

Strong understanding of Technical projects with familiarity of web application technology, electronic document management systems, electronic publishing systems for regulatory filings, and exposure in database technologies and data null

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion,sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military oruniformed service member status, or any other status or characteristic protected by applicable laws, regulations, andordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to [email protected].