Roche

Research Associate III, Assay Transfer

Roche • $69K — $129K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s Degree in Science
  • 4 years of relevant laboratory or industry experience
  • Strong independent thought and troubleshooting skills
  • Proficient in standard software (Excel, Word)
  • Emerging proficiency in statistical analysis tools (e.g., JMP, Minitab)
  • Strong technical writing skills
  • Solid understanding of manufacturing processes and design transfer

Responsibilities

  • Lead the technical transition of product components from Development to Manufacturing
  • Perform pilot reagent manufacturing and testing of pilot reagent builds
  • Coordinate workstreams on cross-functional project teams to meet transfer timelines
  • Write and review manufacturing documents, validation protocols, and technical reports
  • Assist in experimental design and process characterization studies
  • Ensure adherence to GMP, GLP, and Design Control principles
  • Provide technical mentorship and training to junior Research Associates

Benefits

  • Health, dental, and vision insurance
  • 401(k) retirement plan with company match
  • Paid time off and holidays
  • Professional development opportunities
  • Employee wellness programs
Full Job Description

As a Research Associate III in the Assay Transfer team, you will be responsible for leading the technical transition of specific product components from Development to Manufacturing. You will apply advanced scientific principles to ensure manufacturability, lead the preparation of complex manufacturing documents, and identify process improvements. You will operate with significant autonomy, requiring minimal supervision on routine tasks and acting as a technical resource for more junior staff.

The Opportunity

  • Performing pilot reagent manufacturing, including the execution and testing of pilot reagent builds, as a primary responsibility.

  • Representing the Assay Transfer team on cross-functional project teams, coordinating specific workstreams, and ensuring timelines for transfer activities are met.

  • Writing and reviewing complex manufacturing documents, validation protocols, and technical reports with a high degree of accuracy and minimal oversight.

  • Assisting in the design of experiments (DOE) and process characterization studies by helping define variables to be tested and contributing to experimental planning.

  • Ensuring strict adherence to GMP, GLP, and Design Control principles and advocating for "Quality First Time" by reviewing team members’ work.

  • Providing technical mentorship and training to junior Research Associates on laboratory techniques and transfer procedures to support team development and skill enhancement.

Who You Are

  • You hold a Bachelor’s Degree in Science, and 4 years of relevant laboratory/industry experience (required)

Behaviors, competencies, and qualities of the ideal applicant.

  • You demonstrate strong independent thought and the ability to troubleshoot complex assays.

  • You are proficient in standard software (Excel, Word, or equivalent) plus an emerging proficiency in statistical analysis tools (e.g., JMP or Minitab) for data interpretation.

  • You have strong technical writing skills; you are able to draft complete validation reports and standard operating procedures (SOPs) that require only final-stage review.

  • You can present data clearly to the broader group and lead technical discussions regarding specific project components.

  • You have a solid understanding of manufacturing processes and design transfer; familiarity with Lean concepts is a plus.

Relocation benefits are not available for this job posting.

The expected salary range for this position based on the primary location of Tucson is 69,700.00 - 129,400.00 USD Annual.  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

About Roche

Roche Holding AG is a Swiss multinational healthcare company that operates worldwide under two divisions: Pharmaceuticals and Diagnostics. Its holding company, Roche Holding AG, has bearer shares listed on the SIX Swiss Exchange. The company headquarters are located in Basel. Roche is the largest pharmaceutical company in the world, and the leading provider of cancer treatments globally. The company also produces a range of diagnostic tests for medical professionals and patients. Roche was one of the first companies to bring targeted treatments to patients. In 2019, Roche had over 100,000 employees worldwide, and generated revenue of CHF 61.5 billion.
Learn more about Roche
Size
100,920 employees
Industry
NASDAQ

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