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Temporary Assay Development Scientist Jobs in Arizona

Serve as the pathology subject matter expert within the Companion Diagnostics & Oncology business unit, ensuring scientific rigor and clinical relevance in all assay development programs. * Advanced ...

Serve as the pathology subject matter expert within the Companion Diagnostics & Oncology business unit, ensuring scientific rigor and clinical relevance in all assay development programs. * Advanced ...

... assay development, validation activities, and clinical operations. The Manager partners closely with laboratory, clinical, software engineering, IT, quality, and scientific stakeholders to advance ...

Scientist

Tucson, AZ · On-site

$82K - $153K/yr

The Position The Opportunity This position will be responsible for initiating, directing and executing scientific research, development and manufacturing process strategies to support assay ...

... assay development, validation activities, and clinical operations. The Manager partners closely with laboratory, clinical, software engineering, IT, quality, and scientific stakeholders to advance ...

Scientist

Tucson, AZ · On-site

$82K - $153K/yr

The Position The Opportunity This position will be responsible for initiating, directing and executing scientific research, development and manufacturing process strategies to support assay ...

Manager - Bioinformatics

Tempe, AZ · On-site

$140 - $200/hr

... assay development, validation activities, and clinical operations. The Manager partners closely with laboratory, clinical, software engineering, IT, quality, and scientific stakeholders to advance ...

New

Manager - Bioinformatics

Phoenix, AZ · On-site

$150 - $210/hr

... assay development, validation activities, and clinical operations. The Manager partners closely with laboratory, clinical, software engineering, IT, quality, and scientific stakeholders to advance ...

New

To continuously advance science and ensure everyone has access to the healthcare they need today ... You will provide crucial pathology and slide reading support for assay development, FDA submissions ...

To continuously advance science and ensure everyone has access to the healthcare they need today ... You will provide crucial pathology and slide reading support for assay development, FDA submissions ...

Pathologist

Tucson, AZ · On-site +1

To continuously advance science and ensure everyone has access to the healthcare they need today ... Provide crucial pathology and slide reading support for assay development, FDA submissions ...

To continuously advance science and ensure everyone has access to the healthcare they need today ... Provide crucial pathology and slide reading support for assay development, FDA submissions ...

To continuously advance science and ensure everyone has access to the healthcare they need today ... You will provide crucial pathology and slide reading support for assay development, FDA submissions ...

To continuously advance science and ensure everyone has access to the healthcare they need today ... You will provide crucial pathology and slide reading support for assay development, FDA submissions ...

To continuously advance science and ensure everyone has access to the healthcare they need today ... Provide crucial pathology and slide reading support for assay development, FDA submissions ...

To continuously advance science and ensure everyone has access to the healthcare they need today ... You will provide crucial pathology and slide reading support for assay development, FDA submissions ...

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Temporary Assay Development Scientist information

What is the difference between Temporary Assay Development Scientist vs Temporary Quality Control Analyst?

AspectTemporary Assay Development ScientistTemporary Quality Control Analyst
CredentialsBachelor's or Master's in Life Sciences, relevant lab experienceBachelor's in Life Sciences, laboratory experience in quality testing
Work EnvironmentResearch labs, product development teamsQuality control labs, manufacturing support
Industry UsageBiotech, pharmaceutical R&DManufacturing, pharmaceutical QC
Common Search IntentUnderstanding assay development rolesQuality testing and compliance roles

The Temporary Assay Development Scientist focuses on creating and optimizing laboratory assays for new products, often working in R&D settings. In contrast, the Temporary Quality Control Analyst primarily performs testing to ensure products meet quality standards during manufacturing. Both roles require laboratory experience but differ in their focus—development versus quality assurance—making them distinct yet related positions within the biotech and pharmaceutical industries.

What are the key skills and qualifications needed to thrive as a temporary assay development scientist, and why are they important?

To thrive as a Temporary Assay Development Scientist, you generally need a degree in biology, chemistry, or a related field, with experience in assay design, optimization, and validation. Familiarity with laboratory instrumentation, data analysis software, and experience with techniques such as ELISA, PCR, or cell-based assays is typically required. Strong problem-solving abilities, attention to detail, and effective collaboration and communication skills distinguish top performers in this role. These skills ensure reliable assay results, support project timelines, and contribute to the overall success of scientific research and product development.

What is a temporary assay development scientist?

Temporary Assay Development Scientists are professionals hired on a short-term basis to design, optimize, and validate laboratory assays, often for use in research, diagnostics, or pharmaceutical development. Their main role is to ensure that assays are reliable, reproducible, and meet the required standards for scientific or regulatory purposes. These scientists typically work in laboratory settings and may collaborate with other scientists or departments to support ongoing projects. Temporary positions may last from a few months to a year, depending on project needs and funding.

What are some common challenges faced by temporary assay development scientists, and how can they be managed?

Temporary Assay Development Scientists often encounter challenges such as adapting quickly to new laboratory environments, meeting tight project deadlines, and mastering proprietary protocols unique to each organization. Since the role is temporary, there may be limited time to familiarize oneself with existing workflows and team dynamics. Proactively communicating with colleagues, being organized, and seeking clarification early on can help overcome these hurdles. Staying adaptable and open to feedback is key to succeeding in this fast-paced, collaborative setting.
What are the most commonly searched types of Assay Development Scientist jobs in Arizona? The most popular types of Assay Development Scientist jobs in Arizona are:

Subchapter Lead, Head of Pathology

F. Hoffmann-La Roche Ltd

Tucson, AZ • On-site

Other

Re-posted 19 days ago


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.
Roche is the world's #1 provider of companion diagnostics and offers unrivaled experience in developing and commercializing predictive diagnostics that enable personalized treatment strategies for cancer patients. We offer unique opportunities for pathologists interested in playing a role in the development and implementation of new assays critical to our goal of providing more patient access to innovative new therapies.
The Opportunity
As the Subchapter Lead in Clinical Development, Head of Pathology, you will stand at the intersection of cutting-edge science and people leadership. Based in our Tucson, AZ campus, you will lead a world-class team of pathologists dedicated to shaping the future of diagnostics and targeted cancer therapies.
In this role, you provide strategic and scientific leadership while overseeing pathology operations that support more than 100 new and existing product development initiatives and enhancements annually across Primary Antibodies, Special Stains, Digital Pathology, Companion Diagnostics and Instruments. Your team plays a critical role in enabling innovative diagnostics that support precision medicine and targeted cancer therapies worldwide.
In this role, you aren't just managing-you are mentoring, inspiring, and working hands-on with leading-edge technologies to transform patient care globally.

  • People Leadership & Development: Direct, mentor, and foster the professional growth of Instrua highly specialized team of pathologists and 6-7 team leaders. Drive a culture of innovation, collaboration, and continuous learning. Medical oversight for day to day Path Lab activities.
  • Scientific & Clinical Strategy: Serve as the pathology subject matter expert within the Companion Diagnostics & Oncology business unit, ensuring scientific rigor and clinical relevance in all assay development programs.
  • Advanced Assay Development: Guide the team in the development, validation, and implementation of complex assays utilizing top-tier technologies including:
    • Immunohistochemistry (IHC) and in situ hybridization (ISH)
    • Immunofluorescence (IF) and Multiplex assays
    • Digital Pathology and AI-driven image analysis
  • Cross-Functional Collaboration: Partner closely with life science companies, clinical trial teams, regulatory bodies, and internal R&D stakeholders
  • Innovation Champion: Stay ahead of industry trends and emerging pathology technologies to maintain Roche's position as the market leader in companion diagnostics and oncology
Who You Are:
You are a visionary leader who balances deep clinical expertise with a passion for developing people. You thrive in collaborative, fast-paced environments and are motivated by the tangible impact your work has on cancer patients worldwide.
  • You are a MD with US Board Certification in Anatomic Pathology
  • You have 10+ years of people management and leadership within a pharmaceutical, diagnostics, or major academic or medical center environment.
  • You have deep expertise in oncology pathology and hands-on experience with tissue-based biomarkers (IHC, ISH, Multiplex).
  • You have strong familiarity with development processes including digital pathology workflows, image analysis tools, Clinical Case and CAP/CLIA workflows, and CDx development
  • You have excellent communication, negotiation, and stakeholder management skills-ability to translate complex pathology findings to non-clinical teams.

The expected salary range for this position based on the primary location of Tucson, AZ is 255,900-475,300. 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
Relocation benefits are available for this posting
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.