Scientist I, Biology Development
- Employer
- BD
- Location
- Research Triangle Park, North Carolina, US
- Salary
- Competitive
- Closing date
- Jun 27, 2021
View more
- Sector
- Academic / Research
- Field
- Development
- Discipline
- Genetics, Biology
- Salary Type
- Salary
- Employment Type
- Full time
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Job Description Summary
The incumbent will work as a member of the biology group that is responsible for biocompatibility testing on medical devices and materials. Testing is performed in a corporate lab that performs biocompatibility and chemical testing as required by FDA for medical devices and/or therapeutics and in compliance with ISO 10993.
Job Description
The incumbent will work as a member of the biology group that is responsible for biocompatibility testing on medical devices and materials. Testing is performed in a corporate lab that performs biocompatibility and chemical testing as required by FDA for medical devices and/or therapeutics and in compliance with ISO 10993.
- Conducts the appropriate in vitro biological testing in accordance with ISO 10993 and ISO 17025 guidelines, FDA regulations, GLP regulations, and/or other applicable international standards.
- Perform sample preparation and sample extraction.
- Record raw data according to GLP documentation requirements.
- Interpret results and prepare technical reports on completed studies.
- Prepare reagents and solutions needed for testing.
- Collaboration with the Biological Sciences and Quality Assurance group to improve current i_ _n vitro processes.
- Improve data sheets and protocol and report templates.
- Maintain a safe laboratory environment.
Qualifications
- B.S. degree in biology or a related field
- Experience in GLP and ISO 10993 testing guidelines for medical devices preferred
- At least 1-3 years biocompatibility work experience, preferably including work in a GLP or GMP environment
- Well versed in in vitro testing methods
- Proficient in writing protocols and reviewing data and reports for standard testing for medical devices.
- Experience in data interpretation, analysis and technical report writing.
Primary Work Location
USA NC - Research Triangle Park
Additional Locations
Work Shift
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
The incumbent will work as a member of the biology group that is responsible for biocompatibility testing on medical devices and materials. Testing is performed in a corporate lab that performs biocompatibility and chemical testing as required by FDA for medical devices and/or therapeutics and in compliance with ISO 10993.
Job Description
The incumbent will work as a member of the biology group that is responsible for biocompatibility testing on medical devices and materials. Testing is performed in a corporate lab that performs biocompatibility and chemical testing as required by FDA for medical devices and/or therapeutics and in compliance with ISO 10993.
- Conducts the appropriate in vitro biological testing in accordance with ISO 10993 and ISO 17025 guidelines, FDA regulations, GLP regulations, and/or other applicable international standards.
- Perform sample preparation and sample extraction.
- Record raw data according to GLP documentation requirements.
- Interpret results and prepare technical reports on completed studies.
- Prepare reagents and solutions needed for testing.
- Collaboration with the Biological Sciences and Quality Assurance group to improve current i_ _n vitro processes.
- Improve data sheets and protocol and report templates.
- Maintain a safe laboratory environment.
Qualifications
- B.S. degree in biology or a related field
- Experience in GLP and ISO 10993 testing guidelines for medical devices preferred
- At least 1-3 years biocompatibility work experience, preferably including work in a GLP or GMP environment
- Well versed in in vitro testing methods
- Proficient in writing protocols and reviewing data and reports for standard testing for medical devices.
- Experience in data interpretation, analysis and technical report writing.
Primary Work Location
USA NC - Research Triangle Park
Additional Locations
Work Shift
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
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