Associate Molecular Biochemist

Quidel Corporation•Athens, OH

37d•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. The Role The Associate Molecular Biochemist plays a crucial role in GMP molecular chemistry production and in-process quality testing activities. Responsibilities include molecular biochemistry production and quality testing. The Associate Molecular Biochemist will perform routine procedures with senior staff oversite. Some collaboration with senior staff on investigations and troubleshooting is expected. This role is located in Athens, Ohio.

Requirements

BA/BS or MA/MS in life sciences-related field.
1-3 years of relevant industrial, laboratory or collegiate experience or demonstrated mastery of all relevant and associated production and quality related skills for the role.
Background in chemistry, biochemistry, molecular biology, virology, immunology, or related field
Knowledge of assay development, process development, problem-solving, and statistical experimental design
Protein optimization laboratory research experience preferred, particularly in recombinant protein expression.
Ability to complete activities per communicated timelines.
Good organizational skills and an ability to perform multiple tasks simultaneously required.
Good ability to prepare and present technique data
Strong analytical and problem-solving skills.
Ability to work within cross-functional teams.
Excellent communication skills (verbal and written)
Must exhibit professionalism and maturity and display desire to succeed, be self-motivated and proactive
Appropriate computer skills (e-mail, graphing software, word processing) required.
Must possess ability to develop experimental plans and execute associated activities per communicated timelines.

Nice To Haves

Hands on expertise performing protein purification (column-based methods, gravity flow).
Experience with AKTA instrument
Experience with general molecular biology skills such as PCR amplification, primer design, gel electrophoresis and bacterial transformation
Working knowledge of GMP and ISO 13485 quality system regulations

Responsibilities

Execute GMP manufacturing and QC protocols with supervision.
Plan and conduct experiments with the guidance of senior staff, analyzing data and making recommendations for process optimization.
Maintain production inventory and laboratory instruments to support continuous MDx chemistry production and Quality Control.
Identify issues with routine procedures, troubleshoot product performance issues, and implement corrective actions.
Document detailed GMP records and laboratory notebooks accurately to meet internal and external regulatory standards.
Support Process Validation, stability studies and post-market supplemental studies as needed.
Work on problems of a diverse scope and solve technical problems encountered in routine procedures as they arise.
Assist in developing specifications, QC standards, and test methods to ensure product quality and consistency.
Assist customer complaint investigations.
Collaborate in team environment and maintain effective communication with stakeholders.
Ensure a safe working environment by adhering to safety protocols and promoting a culture of safety within the team.