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Sr Bioinformatics Scientist

As a global leader in healthcare, Roche Diagnostics offers a broad portfolio of products, tools and services that help in the prevention, diagnosis and management of diseases like HPV, HIV, hepatitis and diabetes as well as other medical conditions, such as fertility and blood coagulation. These products and services are used by researchers, physicians, patients, hospitals and laboratories worldwide to help improve people's lives.

We are seeking a talented and motivated Senior Bioinformatics Scientist, who will be an integral member of the Sequencing team contributing to the support and development of ground-breaking next-generation sequencing (NGS) products. As a member of Roche’s Sequencing and Life Science (SLS), Scientific Support and Applications team you will apply your expertise in NGS data analysis to support on-market products and perform primary- & secondary-level troubleshooting and Support requests for internal and external customers. You will also serve as a functional expert and support to field application scientists in pre-sales and customer engaging activities proving the necessary technical support in identifying & selecting the best solution that fulfills the customer needs.

To be successful and thrive in this role you will have the ability to work in a fast-paced team environment, interacting with bioinformaticians, laboratory personnel, field application scientists and IT staff committed to providing outstanding customer service. 

 

Primary duties involve:

  • Leading bioinformatics activities for internal applications projects, including consulting during experimental design and working closely with experimental researchers to generate/provide analysis reports, project reports and perform requested custom analyses to ensure that project goals are met within specified timelines.
  • Serving as a functional expert to the technical support team, assisting in investigating and troubleshooting key account customer issues, ensuring that data is received and processed in a systematic, replicable, traceable and timely manner, as well as communicating results to the customer.
  • Serving as a functional expert in pre-sales and customer engaging activities proving the necessary technical support in identifying & selecting the best solution that fulfills the customer needs.
  • Expanding existing and developing new in-house bioinformatics capacity, including the creation, maintenance and utilization of data analysis and visualization pipelines.
  • Ensuring that processed data is made available to internal and external customers in a clear, concise and informative format.
  • Staying current on emerging NGS platforms and applications, along with associated data types and analysis paradigms.

 

    Organization
    Roche
    Organization Website
    Job Location

    200 Ballardvale Street, Suite 250
    Wilmington, MA 01887
    United States

    Requirements

    Minimum requirements:

    Education & years of experience

    • PhD in a relevant subject (Bioinformatics, Computer Science, Computational Biology, or a closely related subject) with 3 years of related experience OR Masters degree in a relevant subject (Bioinformatics, Computer Science, Computational Biology, or a closely related subject) with 8 years of related experience.

    Required skills:

    • Proven hands-on experience designing, developing, documenting and/or deploying bioinformatics pipeline solutions for NGS applications such as whole exome sequencing (WES), RNA-Seq, ChIP-Seq, Methyl-Seq/Bis-Seq, whole genome sequencing (WGS).
    • Proven strong communication skills or customer support experience in highly technical fields like Bioinformatics, Genomics, Biotechnology or in a closely related subject.
    • Demonstrated basic knowledge of statistical/computational methods to solve challenges in like Bioinformatics, Genomics, Biotechnology or in a closely related subject.
    • Demonstrated experience in one or more scripting/programming languages, such as: Python, Jupyter notebooks, R, R markdowns, Bash, C/C#/C++.

    Preferred skills:

    • Familiarity with distributed version control systems, such as git.
    • Familiarity with relational databases, such as PostgreSQL.
    About Our Organization

    At Roche, 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.

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    Pathologist

    Location: Salt Lake City, UT, United States
    Job Identification: 1725
    Job Schedule: Full time

    This Pathologist role for Myriad Genetics is an onsite position located in Salt Lake City, Utah

    Responsibilities

    • Combine his or her expertise in pathology, excellent communication skills, and energetic leadership to help expand a growing menu of tissue-based tests for predictive and personalized medicine in the field of molecular Oncology.
    • Supporting the Director of Anatomic Pathology with oversight of personnel, and quality systems.


    Qualifications

    • M.D. or D.O. with American Board of Pathology board certification in Anatomic Pathology.
    • At least 3-5 years post residency/fellowship experience.
    • Experience with tumor biomarkers.
    • Experience in assay development and implementation in a CLIA laboratory environment.
    • Familiarity with molecular pathology tests using different nucleic acid-based methods.
    • Excellent communication and organizational skills.
    • Demonstrated ability to work in a team environment.


    Physical & Lifting Requirements

    • Lifting Requirements - medium work or exerting up to 50 pounds of force occasionally, 20 pound of force frequently, and 10 pounds of force consistently.
    • Physical Requirements - stationary positioning, moving, operating, ascending/descending, communicating, observing, reaching and repetitive motion.
    • Use of equipment and tools necessary to perform essential job functions.
    • Hazards and Atmospheric Conditions - exposure to fumes, dust, extreme temperatures, wet and/or humid, noise, vibration, mists or gases, mechanical hazards, chemical hazards, electrical hazards and radiant energy hazards. OSHA Category I - duties performed routinely requires exposure to blood, body fluid and tissue.


    #LI-KB1

    About UsMyriad Genetics Inc., is a leading personalized medicine company dedicated to being a trusted advisor transforming patient lives worldwide with pioneering molecular diagnostics. Myriad discovers and commercializes molecular diagnostic tests that: determine the risk of developing disease, accurately diagnose disease, assess the risk of disease progression, and guide treatment decisions across six major medical specialties where molecular diagnostics can significantly improve patient care and lower healthcare costs. Myriad is focused on three strategic imperatives: maintaining leadership in an expanding hereditary cancer market, diversifying its product portfolio through the introduction of new products and increasing the revenue contribution from international markets. For more information on how Myriad is making a difference, please visit the Company's website: www.myriad.com .

    WE ARE AN EQUAL OPPORTUNITY EMPLOYER. Applicants and employees are considered for positions and are evaluated without regard to mental or physical disability, race, color, religion, gender,national origin, age, genetic information, military or veteran status, sexual orientation, marital status or any other protected Federal, State/Province or Local status unrelated to the performance of the work involved.

    Please answer all questions completely. Please do not provide any information not specifically requested on this Employment Application form.

    Apply Here


    PI150946499

    Organization
    Myriad Genetics, Inc
    Job Location

    180 Kimball Way, South San Francisco, CA 94080
    Salt Lake City, UT 84101
    United States

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    New CentoXome: Turning Our Expertise into Your Advantage

    Video

    In this on-demand webinar from Centogene, Aida M. Bertoli-Avella, head of research data analysis, and Jorge Pinto Basto, senior medical director at Centogene, outline the main challenges of rare disease diagnostics, highlight the features of the New CentoXome whole-exome sequencing test, and describe successes of the test in clinical cases.

    Pfizer Centralizes RNA-seq Data on Seven Bridges Under 'Integrative Biology Program'

    Just months into its collaboration with Seven Bridges, Pfizer is moving beyond its original scRNA-seq plans to migrate bulk RNA-seq data to aid R&D.

    SUPER Psychosis Study Presented at ASHG Digs Into Relationships of Rare Variants, Phenotypes

    Using sequence data for tens of thousands of psychotic disease cases and controls, researchers have begun unearthing specific phenotypes linked to rare variants.

    Relocation Specialist

    "As a federal contractor and healthcare company committed to protecting the health and safety of our employees, contractors, customers and communities, employees in the U.S. and Puerto Rico are required to be fully vaccinated against COVID-19, unless an accommodation has been granted for a medical reason or sincerely held religious belief or as otherwise required by applicable law."

     

    GPTW US

    This position is open for remote in Little Rock, AR.

    Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek –– so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com.

     

    Where will your specialized knowledge and technical leadership not only make an impact, but also develop even further? Right here, where you will lead the development and delivery of remote customer relocations by redefining broad concepts into structured projects!

    In this role, the experienced project manager supports the sale and handles the solution design/development of large integrated service projects to external customers; often involving multi-function and multi-vendor efforts!

    The desired candidate for this position can assist with determining overall project plan, budget, structure, schedule, and staffing requirements. They will assist our external customers in the definition and implementation of complex integrated solutions requiring CrossLab services. They are responsible for the pricing of customized solutions and ensuring implementation or delivery within specified goals.

    It is important that this Project Manager can build and maintain client and delivery partner relationships while coordinating internal and external project team members. In addition, the candidate will have a strong attention to detail, will maintain all data and reports, as well as sharing project status and reports with internal and external partners. They will also handle assigned internal projects in support of the development and delivery of Service Support Division (SSD) services and delivery.

    The Ideal Candidate:

    • Demonstrates a commitment to industry accepted project management processes, practices, tools, and behaviors by providing examples of successfully managed projects
    • Assists 3rd Party vendors on-boarding and contracting for assigned projects
    • Is very detail oriented and good at multi-tasking
    • Communicates effectively and lead meetings, and maintain documentation that is shared with customers, sales, and management
    • Is flexible and can an adapt to change, can make tough trade-offs when vital-- within a timeline, project or needs of the department
    • Works well in diverse teams with a sense of urgency, while being willing and able to make course corrections if one path isn't working
    • Has the core values of Trust, Respect, Integrity, and Teamwork and is accountable for their actions

    Job Requirement: * Meet Agilent approved customer/vendor credentialing requirements necessary to gain site access, unless prohibited by law. These requirements vary by customer/vendor and may include, but are not limited to: post-employment background checks, various forms of drug testing, vaccinations, fingerprinting, proof of valid identification, and/or adherence to customer-specific substance abuse programs. Your consent to participate in customer requested screening is a requirement of this position.

    Organization
    Agilent
    Job Location

    Remote Posting Location
    Little Rock, AR 72201
    United States

    Requirements
    • Bachelor's Degree in a relevant scientific field required or equivalent combination of education, training and hands on experience
    • 2+ years of professional work experience
    • Laboratory technical experience, previous instrument relocation experience or laboratory instrument service and maintenance experience (prefer pharmaceutical Instrumentation experience) preferred
    • Basic GMP and GLP experience preferred
    • Lean Six Sigma background and PMP certification highly desirable
    • Familiarity with the following software is required - Microsoft Office (Excel / word / Share Point). Additional software such as Maximo, SAP, or other Data management software, MS Project, Visio, SmartSheet or other project management software knowledge
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    R&D Manager, Software and Firmware

    As a healthcare company committed to protecting the health and safety for our employees, contractors, customers and communities, employees in this role are required to be fully vaccinated against COVID-19, unless an accommodation has been granted for a medical reason or sincerely held religious belief.

    Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications, and expertise. Agilent enables customers to gain the answers and insights they seek -- so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com.

    Agilent is committed to being the premier laboratory partner providing powerful yet easy-to-use sample preparation workflow solutions to our customers. As the R&D Software and Firmware Manager, you will lead the team that is responsible for our flagship VWorks and RapidFire software applications and the embedded firmware in our instruments. These products are continually evolving to provide our customers with modular, scientist-friendly applications that automate all aspects of their sample prep workflows by integrating instruments from across Agilent's portfolio. In this position, you will:

    • Lead the design and development of our Automation software platforms by leveraging on and offshore resources
    • Lead the design and development of firmware for our automated liquid handling and plate handling instruments
    • Lead cross-functional software project teams to release new and enhanced software products in accordance with Agilent's SW PLC process. As the project manager, you will be responsible for running weekly team meetings, project planning, scheduling, risk management and updates to senior management.
    • Utilize the resources on your team to resolve customer issues that are escalated to R&D
    • Develop your team by providing regular feedback and mentoring, conducting annual reviews, and hiring new team members
    • Utilize your hands on software development experience to help solve engineering and research challenges
    Organization
    Agilent Technologies
    Job Location

    5301 Stevens Creek Blvd
    Santa Clara, CA 95051
    United States

    Requirements

    Qualifications:

    Desired Qualifications

    • Bachelor's Degree in Computer Science or similar field
    • A minimum of 5+ years of experience in leading technical teams
    • A minimum of 3+ years in leading cross-functional teams to manage projects
    • Hands-on programming experience in one of the currently used object-oriented programming languages, preferably C++ and C#
    • Experience with projects having real-time, multi-threading, and user experience considerations.
    • Strong software engineering and development process background, including configuration management, Issue Management, continuous integration and related deployment methods and tools (SVN, Jira)
    • Excellent problem-solving skills and a positive demeanor, both within and beyond the team
    • Demonstrated leadership, communication, and social skills.

    Preferred (Nice to have) Qualifications:

    • Experience working with offshore development teams is desirable
    • Experience in serving life science markets and their specific regulatory requirements (specifically 21 CFR Part 11) is desirable.
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    Automation Workflow Engineer

    As a healthcare company committed to protecting the health and safety for our employees, contractors, customers and communities, employees in this role are required to be fully vaccinated against COVID-19, unless an accommodation has been granted for a medical reason or sincerely held religious belief.

    Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications, and expertise. Agilent enables customers to gain the answers and insights they seek –– so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com.

    "What's it like to work at Agilent in R&D? Watch the video"

    Want to be at the cutting edge of Research and Development? Join the team that's taking world-leading Agilent products from design to production. You'll learn about specifying components, how to utilize broad engineering concepts and research techniques, while also documenting research and design specifications.

    Agilent is committed to being the premier laboratory partner providing powerful yet easy-to-use sample preparation workflow solutions to our customers. The successful candidate will leverage their experience programming laboratory robots to migrate manual sample preparation assays onto the AssayMAP and Bravo platforms to enhance workflow data quality and increase sample throughput while decreasing time-to-results and labor costs during drug discovery and development. As an Automation Workflow Engineer, the candidate will be an integral part of an R&D team that develops automated sample preparation workflows on the AssayMAP and Bravo platforms and will be responsible for:

    • translating manual sample preparation processes defined by scientists and analytical chemists into equivalent or better-automated processes for the AssayMAP and Bravo automated liquid handling platforms to create complete sample preparation applications
    • fine-tuning sample preparation applications in collaboration with scientists and analytical chemists to optimize workflow data quality and meet customer needs
    • creating intuitive user interfaces for applications that allow scientists and technicians to efficiently prepare their samples
    • defining and documenting test cases that validate the performance of sample preparation applications
    • collaborating with technical writers to create comprehensive installation and user documentation for sample preparation applications
    • supporting the resolution of customer-reported issues
    Organization
    Agilent Technologies
    Job Location

    5301 Stevens Creek Blvd
    Santa Clara, CA 95051
    United States

    Requirements
    • B.S. or M.S. degree in science or engineering
    • 2+ years of relevant experience required for entry into role.
    • 2+ years of relevant experience related to hands on work programming automated liquid handling systems from Agilent (preferred), Tecan, Hamilton and/or Beckman
    • Possess strong communication and organizational skills
    • Work independently and be self-motivated but also contribute to the success of multidisciplinary teams
    • Experience with biotherapeutic drug discovery/development is desired
    • Experience with Adobe Illustrator and InDesign is desired
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    Program Manager - Lab Operations

    As a healthcare company committed to protecting the health and safety for our employees, contractors, customers and communities, employees in this role are required to be fully vaccinated against COVID-19, unless an accommodation has been granted for a medical reason or sincerely held religious belief.

     

    Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek -- so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com.

     

    This position is open for remote within the following locations: Boston, MA; DE; PA; NJ; CA; Ontario, CAN

     

    Agilent Enterprise Program Managers are primarily responsible for leading and providing oversight for enterprise wide service programs at assigned customer sites! As an Enterprise Program Manager, you will collaborate with the Agilent Enterprise Sales team to develop sales opportunities, design enterprise level support programs to meet the needs of external customers, and insure the implementation and ongoing success of these programs.

     

    You will also be responsible for handling the delivery of large integrated support services solutions to external customers and supporting major enterprise-wide services programs, often involving cross-functional and multi-vendor efforts. The Program Manager will resolve overall program/project plan, budget, structure, schedule, and staffing requirements for these custom programs!

     

    An Enterprise Program Manager:

    • Builds and maintains relationships with clients by having a customer first mentality
    • Assists external customers in the definition and implementation of complex integrated service delivery solutions
    • Is accountable for the success of the overall Enterprise service delivery program
    • Coordinates internal and external project team members' contribution
    • Is responsible for costing of customized solutions and ensuring implementation within budgets
    • Is responsible for the profitability of assigned account(s)

    In addition, an Enterprise Program Manager:

    • Works on project management assignments with broadly defined objectives
    • Solves non-routine issues, challenges and problems within field of specialization
    • Must apply and demonstrate dedication to industry accepted project management processes, practices, tools, and behaviors
    • Is responsible for successful management, implementation, and deployment of assigned customer CrossLab solutions and projects
    • Leads Customer physical inventory and asset tagging activities
    • Provides Cross-functional team leadership that is in line with Agilent policies and procedures
    • Assists with identifying, onboarding and contracting third party service providers to support assigned projects and programs

    Job Requirement:

    Meet Agilent approved customer/vendor credentialing requirements necessary to gain site access, unless prohibited by law. These requirements vary by customer/vendor and may include, but are not limited to: post-employment background checks, various forms of drug testing, vaccinations, fingerprinting, proof of valid identification, and/or adherence to customer-specific substance abuse programs.  Your consent to participate in customer requested screening is a requirement of this position.

     

    As a healthcare company committed to protecting the health and safety for our employees, contractors, customers and communities, employees in this role are required to be fully vaccinated against COVID-19, unless an accommodation has been granted for a medical reason or sincerely held religious belief.

    Organization
    Agilent
    Job Location

    Boston City Limits Remote Location
    Boston, MA 02241
    United States

    Requirements
    • Bachelor's or Master’s in a scientific field or equivalent experience
    • 8+ years of experience, ideally in laboratory instrumentation support and/or sales experience
    • Masters of Business Administration is preferred
    • Project Management Professional certification is an asset
    • Ability to design, price, implement, and handle sophisticated lab instrument service and maintenance programs at customer sites
    • Excellent communication skills
    • 3rd party service provider relationship development and management skills
    • Customer contracting and Scope of Work development experience
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    Scientist (Assay Product Development)

    The Team:

    The Product Development function at CEGX is a focused group of technical specialists whose remit is to take concepts from our Technology Development function and develop them into go-to-market products. Encompassing all aspects of mid to late-stage product development, this team is a mix of innovators, trouble shooters and customer facing scientists who just love to see ideas cross the threshold of concept to product.

    The Role:

    This group is expanding rapidly and we are looking for scientists who have had experience working on mid-late phase consumable/reagent product development projects. With several key products in the pipeline, we are looking for someone who has experience working in an industrial setting and is ready to take ownership of experimental protocols. These would be a blend of molecular, cell and biochemical assays ultimately focused on proving efficacy and robustness of our products.

    This is a brand-new role in a business that is planning on doubling in size in the next 6-12 months; so a great chance to make an early impact and shape the future of CEGX.

    Organization
    Cambridge Epigentix
    Organization Website
    Job Location

    Pembroke Building
    Chesterford Research Park
    Little Chesterford
    CB10 1XL
    United Kingdom

    Salary
    Attractive package that includes equity and annual bonus scheme.
    Benefits

    Company equity

    Pension plan

    Annual bonus scheme

    Requirements

    The Person:

    The ideal candidate will have a strong academic background in the bio-sciences coupled with demonstrable experience in an industrial laboratory. We need individuals that have an understanding of mid-late phase product development, and the experimental data needed at this stage of the lifecycle.

    Key requirements:

    • First degree in relevant biological subject area
    • Experience developing bioassay products or services for biotechnology applications
    • A data-led and analytical approach to work
    • An agile mind-set, happy with a fast moving environment with changing priorities

    This role would suit someone who is already working in a product development team, but is looking for a more dynamic environment with an exciting new product pipeline. As a start-up organisation our employees have an enviable opportunity to take the reins of their career at an exciting time in CEGX’s evolution.

    How to Apply
    About Our Organization

    One of the greatest challenges facing human healthcare is the observation that interventions vary in effectiveness between individuals. Only the advent of DNA sequencing has allowed researchers to understand the underlying cause for this and to pave the way for personalised medicines that couple knowledge of your genetics and epigenetics to your health.

    At Cambridge Epigenetix (CEGX), we are creating a future where sequencing generates more information from DNA and is achievable at far lower costs, bringing closer the day when advanced medicines, diagnostics and personalized treatments become a reality for all. We are creating a technology platform that will deliver a step change in the type of information that can be generated from DNA and the cost at which it can be generated. We expect our technology to become a fundamental component of healthcare and life sciences research.

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    Myriad Genetics: Pamela Wong

    Myriad Genetics has appointed Pamela Wong as its chief legal officer. Wong previously worked for Quest Diagnostics for 14 years, most recently as assistant general counsel. Prior to Quest, she worled for eight years at Baker-McKenzie where she was an intellectual property partner, and at Pillsbury Winthrop Shaw Pittman. She holds a BS degree from the University of California-Berkeley, a PhD from Florida State University-Tallahassee, and a JD from the University of San Diego.