At Genomics England, the systems we run to sequence and store genomic data require cutting edge high-performance computing (HPC) solutions such as NVIDIA DGX for Machine Learning and FPGAs. Our hybrid compute platform supports the groundbreaking research and clinical applications we provide.
As a Senior Product Manager, you’ll be the facilitator of the suite of HPC platform products we offer. This is an opportunity for you to join us to combine your technical, communication, leadership, problem-framing, and problem-solving skills to take responsibility for the HPC products that will directly impact the advancement of genomic medicine.
As the Senior Product Manager, you will be responsible for HPC products throughout their lifecycle. You will work with service owners, other product managers across GEL products, and engineers to understand hosting and compute requirements and develop roadmaps for viable solutions. You’ll interact with HPC solution providers including AWS to identify viable solutions and lead your squad to deliver your roadmap. Your role will be pivotal in shaping the direction of multiple complex products, balancing technical excellence with strong business acumen.
Please note this role is based on a 12 month fixed term contract.
Everyday responsibilities include:
Skills and experience for success:
Essential:
Preferred:
Degree or experience in Bachelor's degree or Advanced degree in Computer Science, Engineering, or a related field.
Salary from £86,000
Being an integral part of such a meaningful mission is extremely rewarding in itself, but in order to support our people, we’re continually improving our benefits package. We pride ourselves on investing in our people and supporting them to achieve their career goals, as well as offering a benefits package including:
Genomics England is actively committed to providing and supporting an inclusive environment that promotes equity, diversity and inclusion best practice both within our community and in any other area where we have influence. We are proud of our diverse community where everyone can come to work and feel welcomed and treated with respect regardless of any disability, ethnicity, gender, gender identity, religion, sexual orientation, or social background.
Genomics England’s policies of non-discrimination and equity and will be applied fairly to all people, regardless of age, disability, gender identity or reassignment, marital or civil partnership status, being pregnant or recently becoming a parent, race, religion or beliefs, sex or sexual orientation, length of service, whether full or part-time or employed under a permanent or a fixed-term contract or any other relevant factor.
Genomics England does not tolerate any form of discrimination, harassment, victimisation or bullying at work. Such behaviour is contrary to our virtues, undermines our mission and core values and diminishes the dignity, respect and integrity of all parties.
Genomics England operates a blended working model as we know our people appreciate the flexibility. We expect most people to come into the office 2 times each month as a minimum. However, this will vary according to role and will be agreed with your team leader. There is no expectation that staff will return to the office full time unless they want to, however, some of our roles require you to be on site full time e.g., lab teams, reception team.
Our teams and squads have, and will continue to, reflect on what works best for them to work together successfully and have the freedom to design working patterns to suit, beyond the minimum. Our office locations are Canary Wharf, Cambridge and Leeds.
As part of our recruitment process, all successful candidates are subject to a Standard Disclosure and Barring Service (DBS) check. We therefore require applicants to disclose any previous offences at point of application, as some unspent convictions may mean we are unable to proceed with your application due to the nature of our work in healthcare.
Genomics England partners with the NHS to provide whole genome sequencing diagnostics. We also equip researchers to find the causes of disease and develop new treatments – with patients and participants at the heart of it all.Our mission is to continue refining, scaling, and evolving our ability to enable others to deliver genomic healthcare and conduct genomic research.We are accelerating our impact and working with patients, doctors, scientists, government and industry to improve genomic testing, and help researchers access the health data and technology they need to make new medical discoveries and create more effective, targeted medicines for everybody.The Participant Panel is made up of a diverse group of people who have consented for their data to be held in the National Genomic Research Library (NGRL). Approved researchers are allowed to access these samples, genomic data, and other associated health data via the Research Environment, a secure, cloud workspace which is sometimes compared to a ‘reading library’: research takes place within it, but the data cannot be taken away.The Panel advises the Genomics England Board and actively engages in decision-making across other committees and boards, playing a vital role in keeping participants’ interests at the heart of everything Genomics England does.The Participant Panel represents the interests of the thousands of people whose data is held by Genomics England. This includes the participants in the 100,000 Genomes Project, COVID-19 patients in the GenOMICC study, and NHS Genomic Medicine Service patients who choose to participate in ongoing research (via the NGRL). It will include others in the future (e.g. cancer cohorts in the UK’s Life Sciences Strategy).The Panel brings direct lived experience as patients or carers of people with rare conditions, COVID-19, or cancer. We work with Genomics England to ensure that the diverse voices of participants, patients and their families are heard and understood at all levels of the organisation. We demonstrate our impact by strategically influencing the decisions made within Genomics England about who uses our sequenced genomes and associated health data, and what they do with it; and by helping Genomics England to engage with patients, participants, their families and the wider public in mutually beneficial ways.
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