Research Associate I/II - CorDx

About You

You are looking to join a team exploding with growth in a lucrative industry that serves people all over the world. You approach assignments with interest and ambition to learn while bringing a strong understanding of laboratory processes that lead to new scientific breakthroughs. You are a team-builder, quick to adapt, and are a trusted source of support for your organization and your team. You are passionate about advancing life-changing technology and are long-term focused.

About Us

CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,000 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare.

Responsibilities

Plan, perform, and record full laboratory processes for in-vitro diagnostic research and development that include but are not limited to the following responsibilities:

• Plans and conducts moderate to complex assessments, evaluations, and studies
• Perform analytical studies such as LOD, Cross-Reactivity, etc.
• Adhere to safety protocols, and BSL-2 requirements.
• Uses various design and statistical tools to aid in study plan creation, data analysis and assessment
• Prepares written reports to summarize, document and communicate findings and recommendations in an efficient and clear manner
• Participates in various product improvement and enhancement efforts
• Maintains accurate and complete R&D records and laboratory notebooks, MSR logs and files

Research Associate II and III positions available, commensurate with experience

Requirements

• 1+ years experience in biotechnology/biology research practices and protocol, title dependent on experience.
• Able to follow instruction with desire and willingness to work effectively independently and/or in cross-functional teams where tact and collaborative efforts prevail
• Strong planning and organizational skills; ability to critically review and summarize data a must
• Effective communication skills (written and verbal) – technical writing a plus
• Working knowledge of Quality Systems Regulations (QSR), Good Manufacturing Practices (GMP) and ISO 13485 standards
• Knowledge of the following scientific related principles, theories and application
  • SDS-PAGE, Western Blot, Antibody Conjugation, ELISA.
• Experience in the In Vitro Diagnostic or medical device manufacturing industry preferred
• Proficient in computer software programs such as MS Word, Excel, Prism.

Benefits

• Medical Insurance Plan
• Retirement Plan
• Paid Time Off
• Training & Development
  
  We are an equal-opportunity employer and celebrate diversity, recognizing that diversity of thought and background builds stronger teams. We approach diversity and inclusion seriously and thoughtfully. We do not discriminate on the basis of race, religion, color, ancestry, national origin, caste, sex, sexual orientation, gender, gender identity or