Şurada gönderildi: Diğer : San Diego | Posted: |
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 applicationSDS-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
Health Care Plan (Medical, Dental, & Vision)
Retirement Plan
Paid Time Off
Family Leave
Training & Development
Company Sponsored Meals
Individual and Team Bonding group spending