Associate Staff Scientist

2 Months ago • 3-5 Years • Research Development

Job Summary

Job Description

Develop, lead, and report on performance studies to ensure products and devices function according to design and regulatory requirements. Responsibilities include planning and designing projects, directing laboratory activities, data monitoring and analysis, troubleshooting, reporting results, and writing study reports. Participation in laboratory work is required when needed. Key tasks involve writing study plans and protocols, training personnel, preparing detailed study reports, overseeing protocol execution, evaluating and verifying data, collaborating with other departments, developing study timelines, managing resources and budgets, presenting study results, and staying updated on regulatory requirements for diagnostic products.
Must have:
  • Ph.D. in a scientific field, or MS with 3+ years industry experience, or BS with 5+ years industry experience
  • 5+ years Microbiology laboratory experience
  • Strong interpersonal skills
  • Excellent oral and written communication skills
  • Ability to plan experiments independently
  • Ability to analyze data and troubleshoot problems in real-time
  • Strong organization and project management skills
Good to have:
  • Knowledge of antimicrobial resistance mechanisms

Job Details

Description

Associate Staff Scientist will develop, lead, and report on performance studies that demonstrate products and devices are functioning in accordance with design and regulatory requirements and specifications. Responsible for planning and designing projects, directing and overseeing laboratory activities, data monitoring and analysis, troubleshooting, reporting results and observations, and writing and reviewing study reports. Participate in laboratory work when required.
 
Job Responsibilities:
  • Write study plans and study protocols that include detailed descriptions of methodology and provide acceptance criteria that succinctly summarize the required study results.
  • Provide training to personnel who will participate in the studies.
  • Write detailed study reports following general guidelines and formats that have been established as effective means of communication to the appropriate regulatory entities.
  • Oversee and participate in the execution of study protocols, data evaluation, and data verification to ensure that the study is conducted and reported appropriately and to help with the identification, communication, and resolution of technical issues.
  • Collaborate with other company personnel in various departments to develop strategies and experiments, share resources, communicate progress and observations, problem-solve, and resolve technical issues.
  • Develop study timelines, determine resource needs, and contribute to project budgets.
  • Compile and present study results and contribute to group discussions, presentations, meetings, and conferences, as needed.
  • Stay current with knowledge of regulatory requirements, guidelines, and expectations for establishing performance of diagnostic products and maintain broad knowledge of state-of-the-art principles and theories.
 
Minimum Requirements
  • Ph.D. in a scientific field, or
    • MS in a scientific field with at least 3 years of relevant industry experience, or
    • BS in a scientific field with at least 5 years of relevant industry experience.
  • 5+ years Microbiology laboratory experience required.
  • Knowledge of antimicrobial resistance mechanisms preferred.
 
Skills and Qualifications:
  • Strong interpersonal skills and the ability to work with a variety of people from different education and cultural backgrounds.
  • Excellent oral and written communication skills.
  • Able to independently plan experiments, analyze data and troubleshoot problems in real-time.
  • Strong organization and project management skills.

Please be aware that recruitment related scams are on the rise. Fraudulent job postings are being placed on other websites, and individuals posing as bioMérieux Talent Acquisition team members are reaching out via email or text message in an attempt to collect your personal and confidential information. In some cases, these scammers are also conducting bogus interviews prior to extending fraudulent offers of employment. Beware of individuals reaching out using general phone numbers and non-bioMerieux email domains (i.e. Hotmail.com, Gmail.com, Yahoo.com, etc.). If you are concerned that an interview experience or offer of employment might be a scam, please make sure you are searching for the posting on our careers site https://careers.biomerieux.com/ or contact us at recruitment@biomerieux.com.

BioMérieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant’s identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMérieux’s or its affiliates’ application process by contacting us via telephone at (385) 770-1132, by email at recruitment@biomerieux.com, or by dialing 711 for access to Telecommunications Relay Services (TRS).

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