Development Associate 1, R+D

The Opportunity

QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing clinical chemistry and transfusion medicine. We are more than 6000 strong and do business in over 130 countries providing answers with fast accurate and consistent testing where and when they are needed most home to hospital lab to clinic.

Our culture puts our team members first and prioritizes actions that support happiness inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all.

The Role

At QuidelOrtho were advancing the power of diagnostics for a healthier future for all. Join our mission as our next Development Associate to support research and new product development. The Development Associate will be responsible for performing experiments as directed by Scientist or Manager.

This position will be onsite full-time at our San Diego CA office (Sorrento Valley).

The Responsibilities

• Supports resolution of product performance issues.
• Collect and summarize experimental data.
• Conducts research process development validations creation and implementation of documentation.
• Maintains project documentation and detailed and organized laboratory notebook records in accordance with internal
• Internal and external regulatory requirements as part of the design control process.
• Assists in developing raw material in process and product specifications.
• Assists in developing QC standards and test methods.
• Supports simple experiments and validation protocols and supports problem solving or trouble-shooting activities under the guidance of a scientist or manager.
• Perform data analysis and interpretation and make recommendations through experimental reports.
• Works on problems of moderate scope and must be able to solve technical problems encountered in routine procedures; receives detailed instructions on new assignments.
• Participates in team environments and interacts with team members professionally.
• Maintains good communication with supervisors and peers.
• Maintains a safe working environment.
• Carries out duties in compliance with established business policies.
• Perform other work-related duties as assigned.

The Individual

Required:

• Education: BS/BA or equivalent in Life Sciences or Chemistry
• Experience: 1-3 years of experience with Chemistry or Life Sciences
• Must have laboratory experience preferably with PCR knowledge and hands on experience.
• Specific technical skills and/or educational background as defined by management based on anticipated and approved projects in agreement with strategic company goals and objectives.
• Good organizational skills and an ability to perform multiple tasks simultaneously.
• Good communication skills (verbal and written).
• Must exhibit professionalism and maturity and display desire to succeed be motivated and proactive.
• Working knowledge of analytical tools used in Chemistry Biochemistry or Immunoassay Development required.
• Desire to actively seek out new job-related responsibilities and learning opportunities.
• Must have basic computer skills (e-mail graphing software word processing) with experience using Microsoft Office (Word Excel PowerPoint).
• Individuals must be able to complete activities per the timelines communicated.
• Exercises judgment within defined procedures and practices to determine appropriate action.
• This position is not currently eligible for visa sponsorship.

Preferred:

• Background in chemistry biochemistry molecular biology virology immunology or related field.
• Basic understanding of GMP and ISO 13485 quality system regulations.

How We Work

At QuidelOrtho our culture is shaped by four core behaviors that guide how we collaborate make decisions and support each other and those we serve. The ideal candidate will exhibit these behaviors as we believe theyre essential to how we thrive as a team and achieve meaningful impact:

• Thrive Together Collaborate intentionally grow as a team
• Make It Happen Focus on priorities embrace continuous improvement
• Commit to Service Cultivate a service mindset
• Embrace Inclusion Be open and authentic welcome diverse perspectives

The Key Working Relationships

Internal Partners:

• Manufacturing Inventory Control Quality Control Purchasing Engineering Document Control and other departments as needed.

External Partners:

• Vendors and suppliers as needed.

The Work Environment

The work environment characteristics are representative of a manufacturing laboratory or warehouse environment and include handling of viral and bacterial hazards potentially hazardous chemicals as well as infectious or potentially infectious bodily fluids tissues and samples. Up to 75% of the time at desk standing or sitting extended periods of time. Flexible work hours to meet project deadlines

Physical Demands

This position has a light physical demand and may include occasional sitting standing walking repetitive movements of hands (i.e. typing and pipetting) light grasping and lifting items weighing up to 20 pounds.

Salary Transparency

The salary range for this position takes into account a wide range of factors including education experience knowledge skills geography and abilities of the candidate in addition to internal equity and alignment with market data. At QuidelOrtho it is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on the facts and circumstances of each case. The salary range for this position is $26/hour to $28/hour and is bonus eligible. QuidelOrtho offers a comprehensive benefits package including medical dental vision life and disability insurance along with a 401(k) plan employee assistance program Employee Stock Purchase Plan paid time off (including sick time) and paid Holidays. All benefits are non-contractual and QuidelOrtho may amend terminate or enhance the benefits provided as it deems appropriate.

Equal Opportunity

QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals including individuals with disabilities have an opportunity to apply for those positions that they are interested in and qualify for without regard to race religion color national origin citizenship sex sexual orientation gender identity age veteran status disability genetic information or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform the duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability please contact us at .

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