Development Associate 1, R+D

QuidelOrtho•San Diego, CA

1d•$26 - $28•Onsite

About The Position

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 6,000 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. At QuidelOrtho, we’re 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).

Requirements

BS/BA or equivalent in Life Sciences or Chemistry
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.

Nice To Haves

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

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.