Staff Program Manager, Software

1 Month ago • 8 Years + • Program Management • $126,800 PA - $190,200 PA

Job Summary

Job Description

As a Staff Program Manager, Software, you will lead and coordinate the development of Research Use Only (RUO) and In Vitro Diagnostic (IVD) Software Products. You will manage complex projects, ensuring timely and budget-conscious completion. You will develop project plans, manage resources, and collaborate with teams to define requirements and address risks. You will also monitor project progress and ensure compliance with relevant regulatory standards. The role involves optimizing project management processes and staying updated with industry trends, including agile software development and cloud computing.
Must have:
  • 8+ years of software product development project leading experience.
  • 4+ years of experience in ISO 13485 regulated environment.
  • Experience leading core teams.
  • Experience with Scaled Agile Framework and/or quarterly planning.
Good to have:
  • Familiar with Medical Device Manufacturing and Design Controls.
  • Business training such as an MBA degree, business certificate, or equivalent.
  • Experience in the genomics industry is highly preferred.
  • Software development/programming experience.
  • Experience integrating deliverables spanning host software, web/cloud, embedded software, and hardware deliveries
Perks:
  • Access to genomics sequencing.
  • Family planning.
  • Health/dental/vision.
  • Retirement benefits.
  • Paid time off.

Job Details

What if the work you did every day could impact the lives of people you know? Or all of humanity?

At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients.

Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible.

Position Summary:

We are seeking a highly skilled and experienced Staff Program Manager to lead and coordinate the development of Research Use Only (RUO) and In Vitro Diagnostic (IVD) Software Products. The successful candidate will be responsible for managing complex projects, ensuring their successful delivery, and collaborating with cross-functional teams to drive innovation in the field of Genomic Analysis. This role offers the unique opportunity to lead a core team in the development of interpretation and analytics products in both the cloud and in the lab (on device).  You will interface with other technology teams and senior leadership to establish scope, schedule, and cost as well as communicating status, issues and risks. 

Responsibilities:

  • Lead a cross-functional leadership team (a.k.a. Core Team) in successfully delivering program commitments.
  • Lead and manage the planning, execution, and delivery of complex RUO and IVD Software Products so they are completed on time, within scope and within budget.
  • Develop comprehensive project plans, timelines, resource management and budgets.
  • Collaborate with software development teams to define project requirements and deliverables.
  • Identify potential risks and issues. Develop and implement effective mitigation strategies. Proactively address challenges to maintain compliance and product quality.
  • Foster effective communication and collaboration among team members and stakeholders.
  • Monitor project progress and report on key performance indicators.
  • Ensure that all IVD software development activities comply with relevant regulatory standards as well as all RUO software development activities comply with the industry standards.
  • Stay up to date with industry trends and emerging technologies, including agile software development and cloud computing.
  • Organize software development activities involving Agile/Scrum methodologies at the team level and a phase-gate lifecycle approach at the enterprise level.
  • Continuously define and optimize software project management and development processes, methodologies, and tools to improve organizational efficiency and effectiveness.
  • Determine resource needs for each project to ensure efficient project execution

Requirements:

  • 8 or more years of experience leading complex software product development projects.
  • 4 or more years of experience leading software product development in an ISO 13485 regulated environment.
  • Experience leading core teams.
  • Experience with Scaled Agile Framework and/or quarterly planning processes.
  • Familiarity with Jira for SW program management
  • In depth knowledge in product development processes with experience following traditional project management methodologies as well as agile software development methodologies. (i.e. phase gate, waterfall etc.).
  • Able to communicate effectively and able to present with confidence, clarity, and focus across all levels of the organization including senior leadership.
  • Demonstrated business judgement navigating complex program challenges to deliver enterprise-scale software successfully according to contract.
  • Demonstrated success championing and delivering improvements to the software development and program management processes of a growing organization.

Preferred Skills & Experience:

  • Familiar with Medical Device Manufacturing and Design Controls for the development of medical devices such as 21CFR820, ISO 13485, and ISO 14971.
  • Business training such as an MBA degree, business certificate, or equivalent
  • Experience in the genomics industry is highly preferred
  • Software development/programming experience.
  • Experience integrating deliverables spanning host software, web/cloud, embedded software, and hardware deliveries
  • Preferred Certifications: PMI PMP, Scrum Master, Scrum Product Owner, SAFe Program Consultant (SPC)

Experience/Education:

  • Typically requires a minimum of 8 years of related experience with a Bachelor’s degree in Computer Science, Math, Engineering, Science, or a related technical discipline; or 6 years and a Master’s degree or better.

#LI-HYBRID

The estimated base salary range for the Staff Program Manager, Software role based in the United States of America is: $126,800 - $190,200. Should the level or location of the role change during the hiring process, the applicable base pay range may be updated accordingly. Compensation decisions are dependent on several factors including, but not limited to, an individual’s qualifications, location where the role is to be performed, internal equity, and alignment with market data. Additionally, all employees are eligible for one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package. We offer a wide range of benefits as innovative as our work, including access to genomics sequencing, family planning, health/dental/vision, retirement benefits, and paid time off.


We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, Illumina has always prioritized openness, collaboration, and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility. We are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. Illumina conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local, state, and federal laws. Background check results may potentially result in the withdrawal of a conditional offer of employment. The background check process and any decisions made as a result shall be made in accordance with all applicable local, state, and federal laws. Illumina prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process, please contact accommodations@illumina.com. To learn more, visit: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf. The position will be posted until a final candidate is selected or the requisition has a sufficient number of qualified applicants. This role is not eligible for visa sponsorship.

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About The Company

At Illumina, our goal is to apply innovative technologies and revolutionary assays to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. These studies will help make the realization of personalized medicine possible. With such rapid advances in technology taking place, it is mission critical to have solutions that are not only innovative, but flexible, scalable, and complete with industry-leading support and service. As a global company that places high value on collaborative interactions, rapid delivery of solutions, and prioritizing the needs of its customers, we strive to meet this challenge. Illumina’s innovative, array-based solutions for DNA, RNA, and protein analysis serve as tools for disease research, drug development, and the development of molecular tests in the clinic.



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