Global Project Manager, Companion Diagnostics

Davita Inc.; Tucson (AZ); Hybrid; USD 84,000 - 157,000; Full time

Job summary

A leading company in healthcare innovation seeks a Global Project Manager in Tucson, AZ. You will lead various projects from concept to completion, manage resources, and ensure optimized delivery of healthcare products. Required qualifications include a Bachelor's degree and substantial experience in project management within the medical field, particularly in diagnostics or biotech.

Qualifications

• 6 years of experience in project management in the diagnostic, medical device, pharmaceutical, or biotech industry.
• 1+ years in clinical biomarker or In Vitro Diagnostic development.
• Experience in a regulated industry (e.g. FDA, ISO 13485).

Responsibilities

• Own project structures for Assay product development including communication management and progress control.
• Drive integrated project plans allowing teams to work efficiently.
• Coach team members in project management methodologies.

Skills

Project Management

Agile Methodology

Communication Management

Risk Management

Education

Bachelor's degree

Master's degree

Job description

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That's what makes us Roche.

As part of the Project Management Chapter, the Global Project Manager (GPM) plays a key role in optimized product delivery and is 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 Global Project Manager 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.

The Opportunity:

• You will own project/program/product structures for Assay product development & product care activities including communication management, timelines, resource and budget plans, progress and cost control, and risk management.

• You will proactively own and drive integrated project plans including dependencies, resources and budgets allowing the teams to work efficiently and effectively.

• You will select project methodology and apply agile best practices as appropriate, including coaching and guiding teams in project methodology including agile practices (with Project/Program Leads or PMC management if appropriate).

• You will lead project team meetings and fosters knowledge sharing between project/product teams and sub-chapters to enhance project effectiveness and optimized delivery.

• You will work closely with Sub-Chapter Leads, Network Leads, Functional Partners, Finance, Portfolio Management, Analytics & Insights and other chapters to ensure an optimized project delivery.

• You will coach other members of the project/product team as well as peers in all key areas of Project Management expertise.

• You will support the development and implementation of key Portfolio and Project Management (PPM) functional initiatives.

Who You Are:
(Required)

• You hold a Bachelor's degreefrom an accredited institution

• You have6 years of experience in project management / engineering/ business in the diagnostic, medical device, pharmaceutical or biotech industry leading product development and product care projects.

• You have 1+ years of experience in clinical biomarker or In Vitro Diagnostic development, companion diagnostic development, analytical and clinical validations, regulatory submissions, instrument/systems development, or program management

• You have 1+ years of experience in a regulated industry (e.g. FDA 21 CFR part 820, ISO 13485, ISO 9001).
  

Preferred Qualifications:

• You have a Master's degree from an accredited institution along with 4 years of experience in project management / engineering/ business experience in the diagnostic, medical device, pharmaceutical or biotech industry leading product development and product care projects.

• You have 3+ years in clinical biomarker or In Vitro Diagnostic development, companion diagnostic development, analytical and clinical validations, regulatory submissions, instrument/systems development, or program management

This is an onsite/hybrid position aligning with Roche Diagnostics onsite requirements. This position is based in Tucson, AZ.

Relocation assistance is not available for this job posting.

The expected salary range for this position based on the primary location of Tucson, AZ is $84,500 - $157,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.

This position also qualifies for the benefits detailed at the link provided below.
Benefits

Who we are

A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let's build a healthier future, together.

Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.