drjobs Research Associate 1 IVD Product Support

Research Associate 1 IVD Product Support

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1 Vacancy
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Job Location drjobs

Austin - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

POSITION SUMMARY:

TheProduct Development Research Associate will contribute to the design of studies and actively participate in laboratory experiments and/or logistical tasks in collaboration with others to support product development and verification and validation (V&V) studies under design control for next generation sequencing (NGS) assays. We are looking for a meticulous and dedicated candidate with handson laboratory experience in assay development who can work effectively in a fastpaced environment to ensure the highest quality clinical assays are developed and launched for our patients. The ideal candidate will be an enthusiastic flexible team member who learns quickly enjoys multitasking and most importantly has an interest in our company and our products.

PRIMARY RESPONSIBILITIES:

  • Assist with the designing planning and executing of development and V&V laboratory experiments using various molecular biology and general laboratory techniques to prepare samples for Next Generation Sequencing
  • Perform library preparation for NextGen sequencing using automated and manual methods
  • Determine quantity and/or quality of nucleic acids using QuantIT Qubit BioAnalyzer and qPCR
  • Coordinate across multiple internal groups (laboratory operations scientific operations CLIA Quality Assurance)
  • Participate in the planning of logistical workflow processes and suggest process improvements to subject matter experts as needed
  • Perform basic data analysis (JMP) and maintain a detailed and organized laboratory notebook and accurate records of lab work using a variety of software including Google Sheets Microsoft Excel and internal databases
  • Periodically review standard operating procedures (SOP) and other work instructions. Assisting in the development and writing of laboratory procedures and techniques.
  • Receive and process laboratory specimens following standard methods and procedures with meticulous attention to detail.
  • Identifying necessary kits and reagents for development and production sets and locating them via inventory or freezer maps.
  • Performing physical transfers of reagents from freezers to designated locations for production use.
  • Recording all stock movements and issues using inventory control systems.
  • Track samples using LIMS database queries and advanced Excel techniques; verify the accuracy of specimens being processed and analyzed
  • Adapt to handle multiple tasks and priorities and perform other duties as assigned
  • Learn the science behind ongoing research projects while actively completing increasingly complex tasks

QUALIFICATIONS:

  • Bachelors degree in molecular biology genetics biochemistry cell biology or related field
  • Minimum of 12 year of Molecular Biology laboratory experience and or relevant industry experience in a research and/or assay development setting

KNOWLEDGE SKILLS AND ABILITIES:

  • Must have handson experience with good pipetting practices (single and multichannel micropipettes serological pipettes)
  • Handson experience with nucleic acid techniques (purification quantification amplification using PCR qPCR QuantIT/Qubit BioAnalyzer or TapeStation)
  • Handson experience with NGS library preparation and Illumina sequencing platforms highly preferred (NovaSeq NextSeq iSeq etc. is highly desired
  • DNA extraction from biological samples.
  • Working knowledge of laboratory safety Good Laboratory Practices (GLP) and regulatory standards such as CLIA requirements.
  • Able to operate independently in a fastpaced lab under general supervision managing multiple tasks and priorities with minimal errors.
  • Ability to lift up to 20 lbs frequent standing and walking occasional sitting etc. Occasional exposure to cold temperatures.
  • Effective communication skills including gathering information from different teams communicating with suppliers writing protocols and summarizing results in reports or presentations
  • Excellent with Microsoft Office programs and Google Drive including Docs Sheets Slides and Forms
  • Ability to think creatively and analytically with strong troubleshooting and problemsolving skills
  • Team player with demonstrated strong interpersonal skills with an ability to build effective working relationships within functional area

OUR OPPORTUNITY

Natera is a global leader in cellfree DNA (cfDNA) testing dedicated to oncology womens health and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer healthier lives.

The Natera team consists of highly dedicated statisticians geneticists doctors laboratory scientists business professionals software engineers and many other professionals from worldclass institutions who care deeply for our work and each other. When you join Natera youll work hard and grow quickly. Working alongside the elite of the industry youll be stretched and challenged and take pride in being part of a company that is changing the landscape of genetic disease management.

WHAT WE OFFER

Competitive Benefits Employee benefits include comprehensive medical dental vision life and disability plans for eligible employees and their dependents. Additionally Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave 401k benefits commuter benefits and much more. We also offer a generous employee referral program!

For more information visit .

Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment and welcome people of different backgrounds experiences abilities and perspectives. Inclusive collaboration benefits our employees our community and our patients and is critical to our mission of changing the management of disease worldwide.

All qualified applicants are encouraged to apply and will be considered without regard to race color religion gender gender identity or expression sexual orientation national origin genetics age veteran status disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories consistent with applicable laws.

If you are based in California we encourage you to read this important information for California residents.

Link: be advised that Natera will reach out to candidates with a @ domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously and will collaborate with law enforcement authorities to prosecute any related cyber crimes.

For more information:
BBB announcement on job scams
FBI Cyber Crime resource page


Required Experience:

IC

Employment Type

Full Time

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