Global Project Manager - Personalized Healthcare
Company: SQA Solution
Location: Tucson
Posted on: February 16, 2026
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Job Description:
Job Description Job Description Type : Contract, W2 only
Duration : 12 months Location : Tucson, AZ (hybrid - 2 days/week
on-site) Pay : $ 58/-$62/hr max, DOE, all-inclusive Please note
that at this time we are unable to sponsor employment authorization
(both new and transfer) Description: The Global Project Manager
(GPM) plays a key role in optimized product delivery, accountable
for all project management aspects of various projects from simple
to complex in nature. Drives the project/product from the original
concept through completion by developing and directing detailed
work plans, schedules, project estimates, spending, resource plans,
and status reports. As a trusted advisor, the GPM translates and
drives projects into products and enables the organization to use
energy and time effectively and efficiently while quickly
responding to changing business needs across the portfolio.
Responsibilities: Drive the delivery of innovative Companion
Diagnostics projects, working with both internal project
stakeholders as well as external Pharma partners. Own
project/program/product structures for product development and
product care activities, including communication management,
timelines, resource and budget plans, progress, and cost control.
Create, coordinate, and maintain integrated project plans,
including dependencies, resources, and budgets, allowing teams to
work efficiently and effectively. Be accountable for quality
implementation in complex projects in the following areas: project
risk management, critical path analysis, scenario creation and
analysis, budget analysis, and robust planning. Proactively
identify gaps, potential bottlenecks or delays, challenge
assumptions, and propose innovative options to close gaps and get
complex projects back on track while communicating issues
proactively to stakeholders. Consistently execute project
management processes, including guiding and managing preparation
for milestone reviews, capacity reviews (cQCR, SCR & fQCR), etc.,
as applicable, and may lead improvement initiatives. Select project
methodology and apply Agile methods as appropriate, including
coaching and guiding teams in project methodology, including Agile
practices (with Project/Program Leads or PMC management if
appropriate). Lead meetings and foster knowledge sharing between
project/product teams to enhance project effectiveness and
optimized delivery. Establish, measure and report Key Performance
Indicators (KPIs), standard metrics, Objectives and Key Results
(OKRs) or Outcome Based Planning (OBPs) key results for projects,
enabling teams and functions to measure and improve quality,
efficiency, and effectiveness. Act as a trusted advisor with a 360
view on all levels to advise and support the project/product teams
as well as the broader organization in holistic planning, project
risk management, scenario creation as well as critical path
analysis, with the aim to ensure optimized value delivery. Be the
single point of contact and control for project and program data
collected from the functions. Act as Agile Program Manager as
defined by Scaled Agile Framework (SAFe) where applicable.
Requirements: Bachelor's degree in science, engineering or business
related fields. 4 years of project management experience in the
diagnostic, medical device, health science, pharmaceutical or
biotech industry leading complex new, product development and
product care projects. Project management experience in other
regulated industries will also be considered. Demonstrated
experience using Planisware, MS-Office, G-Suite and know-how of
project management tools such as Trello, LucidChart, Smartsheet,
Jira, Azure DevOps, etc. 1 year of experience in clinical biomarker
or In Vitro Diagnostic development, companion diagnostic
development, analytical and clinical validations and regulatory
submissions or instrument development and program management
(preferred). 1 year of experience in a regulated industry (e.g. FDA
21 CFR part 820, ISO 13485, ISO 9001) Experience driving the
delivery of high-complex product development projects, from
conceptualization to commercialization. Knowledge of relevant
Design Control and/or Phased Development processes. Knowledge of
healthcare quality, risk, and/or regulatory compliance. PMP
Certification and SAFe Certification (preferred). We are an Equal
Opportunity employer and welcome talent across all aspects of
background, orientation, origin, and identity in an inclusive and
non-discriminatory way. Applicants receive consideration without
bias and based on the relevant qualifications, talents, skills,
experiences, and business needs
Keywords: SQA Solution, Maricopa , Global Project Manager - Personalized Healthcare, Executive , Tucson, Arizona
