Development Associate I

Posted 9 Days Ago
Be an Early Applicant
Ridgecrest Estates, CA
57K-78K Annually
1-3 Years Experience
Healthtech • Biotech
The Role
The Development Associate I at QuidelOrtho supports research and new product development by conducting experiments, collecting data, and maintaining project documentation. They work on problem-solving activities under the guidance of a scientist or manager, and maintain good communication with team members and supervisors.
Summary Generated by Built In

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 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.

The Role

The Development Associate I participates in activities to support research and new product development. The position performs simple experiments as directed by Scientist or Manager. The position is based in the Summers Ridge location in San Diego, California.

The Responsibilities

  • Supports resolution of product performance issues

  • Collects 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 Quidel 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

  • Support simple experiments and validation protocols and supports problem solving or trouble-shooting activities under the guidance of a scientist or manager

  • Performs data analysis and interpretation and makes recommendations through experimental reports

  • 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

  • BS/BA or equivalent in life sciences or chemistry and skills associated with 1-3years of experience required.

  • Background in chemistry, biochemistry, molecular biology, virology, immunology, or related field required.

  • 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 required.

  • Good organizational skills and an ability to perform multiple tasks simultaneously required.

  • Good verbal and written communication skills required.

  • Professionalism and maturity and display of a desire to succeed, be motivated and proactive required.

  • Working knowledge of analytical tools used in Chemistry, Biochemistry, or Immunoassay Development required.

  • Basic understanding of GMP and ISO 13485 quality system regulations preferred

  • Demonstrate willingness and ability to work cross-functionally in other areas preferred.

  • Desire to actively seek out new, job-related responsibilities and learning opportunities required.

  • Appropriate computer skills (e-mail, graphing software, word processing) required.

  • Works on problems of moderate scope and must be able to solve technical problems encountered in routine procedures; receives detailed instructions on new assignments.

  • Individual must be able to complete activities per communicated timelines. 

  • Exercises judgment within defined procedures and practices to determine appropriate action.

The Key Working Relationships

Internal Partners:

Interacts with Manufacturing, Inventory Control, QC, Purchasing, Engineering, Document Control and other resources as needed under the direction of supervisor/scientist.

The Work Environment

The work environment characteristics are representative of both an office and laboratory environment and include handling of viral and bacterial hazards as well as infectious or potentially infectious bodily fluids, tissues and samples.

The Physical Demands

Position requires ability to lift up to 20 lbs. on a regular basis. Walking, standing, and sitting for long periods of time (up to 75% of the day) are routine to accomplish tasks in this role. Specific vision abilities required by this job include close and distance vision and the ability to adjust focus. Personal protective equipment is required as posted.

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 $57,000.00 - $78,000.00 annually. 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 Employment 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 their 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 [email protected] .


 

The Company
HQ: Raritan, NJ
4,457 Employees
On-site Workplace

What We Do

Ortho Clinical Diagnostics (Nasdaq: OCDX) is one of the world’s largest pure-play in vitro diagnostics (IVD) companies dedicated to transforming patient care.

More than 800,000 patients across the world are impacted by Ortho’s tests each day. Because Every Test is a Life, Ortho provides hospitals, hospital networks, clinical laboratories and blood banks around the world with innovative technology and tools to ensure test results are fast, accurate, and reliable. Ortho's customized solutions enhance clinical outcomes, improve efficiency, overcome lab staffing challenges and reduce costs.

From launching the first product to determine Rh+ or Rh- blood type, developing the world’s first tests for the detection of antibodies against HIV and hepatitis C, introducing patented dry-slide technology and marketing the first U.S. Food and Drug Administration-authorized high-volume antibody and antigen tests for COVID-19, Ortho has been a pioneering leader in the IVD space for over 80 years.

The company is powered by Ortho Care, an award-winning, holistic service and support program that ensures best-in-class technical, field and remote service and inventory support to laboratories in more than 130 countries and territories around the globe.

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