Production Biochemist I
Athens, OH 
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Posted 30 days ago
Job Description
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

As we continue to grow we are seeking a Production Biochemist I at our Athens, Ohio facility. The Production Biochemist I ELISA is responsible for ELISA immunoassay production in accordance with Quidel's Quality System Regulations.

The Responsibilities
  • Perform wet chemistry and analytical testing practices for ELISA immunoassay production. Responsible for the manufacture and coordination of testing of all reagents represented in the work order assignments.

  • Performs multiple ELISA immunoassays daily with established protocols while being responsible for the production of reagents and buffers used in those assays as well as the coordination of testing qualifications with fellow Biochemist.

  • Create and maintain production timelines for work order assignments. Summarize daily progress and presents results to supervisor in a logical manner either in verbal or written reports.

  • Perform optimization to the production bulk solutions to meet required product specifications. Identify assay-related complications and assists in the resolution with supervisor or trainers.

  • Effectively operates a range of laboratory instrumentation and may perform instrument verifications and/or maintenance if required. Key instruments and software required are plate reader with Softmax Pro.

  • Perform validation procedures for immunoassay methods under supervision and edit assay protocols for review by Supervisor

The Individual

Required

  • Bachelor's Degree in a biology, biochemistry, chemistry or other related science field with <1-year specific laboratory experience outside course work.

  • An equivalent combination of education and experience will also be considered if related and applicable to job requirements.

  • Strong core competency in biochemistry, chemistry, immunology and biology

  • Ability to set-up custom spreadsheets and analysis templates in various data analysis or equipment software for daily examination, interpretation and trend identification to determine suitable progression of production timeline.

  • Proficient at sustained communication with supervisor and cross functional teams on daily production progress and key project initiatives. Expertise in organization and time management will be key for production success.

  • Compliance procedures defined by a set of standards regulated by requirements from FDA, any export countries and ISO organizations

  • Excellent oral and written communication skills, analytical skills, organizational skills, flexibility, attention to detail, and strong interpersonal skills

Preferred

  • Experience with microtiter-based assays (ELISA); microplate readers/software

The Key Working Relationships

Internal Partners:

Packaging, R&D, Supply Chain, Purchasing, QC, QA, and Customer Service groups

The Work Environment

Laboratory and manufacturing environment. The ability to use a computer keyboard, sit or stand for long hours, and handle routine laboratory equipment is essential to this position. Must be able to visually monitor testing procedures and results for Quality Standards. Equipment maintenance requires ability to maneuver throughout both laboratory and office environments and to lift up to 45 pounds.

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 .

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Equal employment opportunities for all employees. We fulfills this commitment through a variety of measures including internal & external posting of job openings, hiring, training & promoting individuals without regard to race, color, religion, sex, pregnancy, national origin, ancestry, citizenship, veteran status, disability, medical condition, marital or domestic partner status, sexual orientation, gender identity, age,or any other considerations made unlawful by federal,state or local law

 

Job Summary
Company
Start Date
As soon as possible
Employment Term and Type
Regular, Full Time
Required Education
Bachelor's Degree
Required Experience
1+ years
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