What Jobs are available for Researchers in Tucson?

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**
**Summary:**
In this position you will be responsible for conducting research, development and manufacturing laboratory experimentation and other scientific activities to support Ventana projects. Exercises technical expertise and discretion in the design, execution and interpretation of experiments that contribute to project strategies. Prepares technical reports, summaries, protocols and quantitative analyses. Presents and discusses results of experiments within department and project team. Maintains high level of professional expertise through familiarity with scientific literature and may participate in conferences and professional societies. Follows company policies and procedures for GMP, GLP, Design Control and others as appropriate. Maintains complete and accurate laboratory documentation and electronic files. May act as principal investigator in conducting own experiments.
**The Opportunity:**
Your responsibilities in this role will include:
+ Designs a wide range of experimental protocols
+ Executes bench experiments; makes detailed and general observations and analyzes data.
+ Prepares technical reports, summaries and qantitative analyses.
+ Maintains complete and accurate records.
+ Normally receives general directions on routine work and detailed directions on new assignments.
+ Makes suggestions to improve work processes and laboratory environment.
+ Recognizes and documents activities for publication and/or patent potential.
+ Works on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors.
+ Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.
+ May participate in cross functional technical teams such as a failure investigation team.
+ Works well in a team environment by being a productive project team member, suggesting creative solutions to problems and providing input to project planning.
+ Trains others in areas of expertise.
+ Troubleshoots problems and institutes corrective action.
+ Prepares and presents experimental procedures and results in group and project teams.
+ Monitors work to ensure quality, and continuously promote Quality First Time.
+ Other duties as assigned by management.
**Qualifications:**
+ Bachelor's Degree in Science with 2-4 years relevant experience preferred orMaster's Degree in Science with 0-2 years relevant experience preferred
+ Knows basic and a range of specialized laboratory techniques.
+ Capable with searching scientific literature to gain information about specific topics.
+ Skilled with use of word processing, spreadsheets, graphical and presentation software applications.
This position is 40 hr/week on-site
Relocation benefits are not available for this posting
The expected salary range for this position based on the primary location of Tucson, Arizona is $68,300 - $126,800.00. 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 ( 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 ( .

Our client, a world leader in diagnostics and life sciences, is looking for a "Research Associate II - Assay Transfer”  based out of Tucson, AZ .

Job Duration: Long term Contract (Possibility Of Further Extension)

Pay Rate : $34/hr on W2

Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K

This role ensures successful design transfer, manufacturability, and compliance with GMP standards, directly impacting product quality and reliability.

Key Responsibilities

Execute R&D activities to ensure product, method, and process manufacturability.

Manufacture GMP lots and participate in process characterizations for reagent transfer to Manufacturing.

Prepare and maintain manufacturing documents, technical reports, summaries, and quantitative analyses.

Collaborate cross-functionally on design transfer activities to support smooth scale-up.

Maintain accurate documentation and present/discuss data within and across teams.

Provide training in areas of expertise and foster a culture of “Quality First Time.”

Apply Scaled Agile Framework (SAFe) principles to prioritize and complete work as a member of the Assay Transfer Agile team.

Required Qualifications

BS degree in a related scientific field.

5+ years of post-graduate experience working in a scientific laboratory within industry.

5+ years of experience in a GMP/manufacturing environment.

Strong documentation, communication, and collaboration skills.

Experience in Quality Control or formulations a plus.

If interested, please send us your updated resume at

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**Job Description**
**Job Summary**
Provides entry level analyst support for claims research activities. This role plays a pivotal role in ensuring the timely and accurate resolution of provider-submitted claims issues. This role requires a keen understanding of medical claims processing, strong analytical skills, and the ability to effectively triage issues to the appropriate department for further investigation or correction. This is a production-based role, with clear expectations for meeting production and quality standards.
**Job Duties**
+ Reviews and analyzes claims-related issues submitted by providers to identify potential root causes quickly and accurately.
+ Triages issues based on type and complexity, assigning them to the appropriate department or team for further research or correction.
+ Leverages knowledge of claims processing workflows, billing practices, and regulatory guidelines to provide accurate assessments.
+ Meets quality and production goals.
+ Maintains detailed records of claim reviews and resolutions.
+ Identifies trends in submitted issues to inform process improvements and reduce recurring errors.
+ Provides feedback and recommendations for process improvements.
+ Completes training and development activities to stay current with industry standards and best practices.
**Job Qualifications**
**REQUIRED QUALIFICATIONS:**
+ At least 1 year of experience in claims processing or operations or equivalent combination of relevant education and experience
+ Basic knowledge of medical billing and basic claims processes.
+ Problem-solving skills
+ Verbal and written communication skills and ability to collaborate
+ Ability to work independently and as part of a team
+ Microsoft Office suite/applicable software program(s) proficiency
**PREFERRED QUALIFICATIONS:**
+ Experience with process improvement methodologies.
+ Knowledge of industry regulations and compliance standards.
+ Familiarity with systems used to manage claims inquiries and adjustment requests
+ Understanding of billing and coding procedures
+ Experience with Medicaid, Medicare, and Marketplace claims
To all current Molina employees: If you are interested in applying for this position, please apply through the Internal Job Board.
Molina Healthcare offers a competitive benefits and compensation package. Molina Healthcare is an Equal Opportunity Employer (EOE) M/F/D/V.
Pay Range: $21.16 - $38.37 / HOURLY
*Actual compensation may vary from posting based on geographic location, work experience, education and/or skill level.