ICONMA
Our Client, a Biotech company, is looking for a US_Scientist I_CO for their Santa Clara, CA location.
Responsibilities
Under close supervision, conducts lab experiments following safety guidelines.
Work from and understand protocols provided. Appropriately documents experimental details in eLN and follows RMD guidance documents for ensuring data integrity.
May provide experiment details and conclusions for design history files.
May troubleshoot issues related to experiments. Execute activities within the assigned timeframe.
Is capable of analyzing experimental data using basic skills and existing templates created for the purpose. Is able to follow protocols for data analysis with supervision.
Communication (written and verbal)
Communicates results to supervisor in a timely manner. Uses basic technical writing skills to write lab reports in eLN and DHFs (e.g., protocols and reports). May present findings at group meetings Ability to receive and provide feedback.
May establish professional relationships, as appropriate. May participate in active collaboration within Development. Accountable and responsible for creating and maintaining a culture of respectful and professional interactions among the entire team.
Participates in routine lab maintenance, lab safety, ISO, and QSR implementation. May track laboratory inventory (e.g., equipment, supplies, specimens, raw materials, reagents).
Has basic understanding of molecular/microbiology and biochemical concepts (e.g., PCR, sterile technique, calculations). Familiar with assay and platform.
Requirements
Be aware of project timelines and actively contribute towards the completion of project goals.
Accountable for own career development and engagement. Demonstrate Roche cultural beliefs and growth mindset
Function: Assay Development
strong critical thinking and problem solving skills with a meticulous attention to detail, effective communication and interpersonal skills to work across a multitude of functional areas, good organizational skills, self-motivated and able to manage time effectively to meet project timelines, can work independently and as part of a team in a fast-paced timeline driven environment
Expertise in DNA/RNA isolation, proficiency in PCR, qPCR, and digital PCR applications preferred, strong proficiency in data analysis using statistical tools (e.g. JMP)
Min years: 0-5 years
Highly motivated and skilled scientist needed to contribute to Assay Development support of on-market products and potential development of new companion diagnostic assays in the Oncology and Client area.
Why Should You Apply?
Health Benefits
Referral Program
Excellent growth and advancement opportunities
As an equal opportunity employer, ICONMA provides an employment environment that supports and encourages the abilities of all persons without regard to race, color, religion, gender, sexual orientation, gender identity or express, ethnicity, national origin, age, disability status, political affiliation, genetics, marital status, protected veteran status, or any other characteristic protected by federal, state, or local laws
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Responsibilities
Under close supervision, conducts lab experiments following safety guidelines.
Work from and understand protocols provided. Appropriately documents experimental details in eLN and follows RMD guidance documents for ensuring data integrity.
May provide experiment details and conclusions for design history files.
May troubleshoot issues related to experiments. Execute activities within the assigned timeframe.
Is capable of analyzing experimental data using basic skills and existing templates created for the purpose. Is able to follow protocols for data analysis with supervision.
Communication (written and verbal)
Communicates results to supervisor in a timely manner. Uses basic technical writing skills to write lab reports in eLN and DHFs (e.g., protocols and reports). May present findings at group meetings Ability to receive and provide feedback.
May establish professional relationships, as appropriate. May participate in active collaboration within Development. Accountable and responsible for creating and maintaining a culture of respectful and professional interactions among the entire team.
Participates in routine lab maintenance, lab safety, ISO, and QSR implementation. May track laboratory inventory (e.g., equipment, supplies, specimens, raw materials, reagents).
Has basic understanding of molecular/microbiology and biochemical concepts (e.g., PCR, sterile technique, calculations). Familiar with assay and platform.
Requirements
Be aware of project timelines and actively contribute towards the completion of project goals.
Accountable for own career development and engagement. Demonstrate Roche cultural beliefs and growth mindset
Function: Assay Development
strong critical thinking and problem solving skills with a meticulous attention to detail, effective communication and interpersonal skills to work across a multitude of functional areas, good organizational skills, self-motivated and able to manage time effectively to meet project timelines, can work independently and as part of a team in a fast-paced timeline driven environment
Expertise in DNA/RNA isolation, proficiency in PCR, qPCR, and digital PCR applications preferred, strong proficiency in data analysis using statistical tools (e.g. JMP)
Min years: 0-5 years
Highly motivated and skilled scientist needed to contribute to Assay Development support of on-market products and potential development of new companion diagnostic assays in the Oncology and Client area.
Why Should You Apply?
Health Benefits
Referral Program
Excellent growth and advancement opportunities
As an equal opportunity employer, ICONMA provides an employment environment that supports and encourages the abilities of all persons without regard to race, color, religion, gender, sexual orientation, gender identity or express, ethnicity, national origin, age, disability status, political affiliation, genetics, marital status, protected veteran status, or any other characteristic protected by federal, state, or local laws
#J-18808-Ljbffr