US
0 suggestions are available, use up and down arrow to navigate them
PROCESSING APPLICATION
Hold tight! We’re comparing your resume to the job requirements…
ARE YOU SURE YOU WANT TO APPLY TO THIS JOB?
Based on your Resume, it doesn't look like you meet the requirements from the employer. You can still apply if you think you’re a fit.
Job Requirements of Biocompatibility / Toxicology Expert:
-
Employment Type:
Full-Time
-
Location:
Raleigh, NC (Onsite)
Do you meet the requirements for this job?
Biocompatibility / Toxicology Expert
Bayone Solutions Inc
Raleigh, NC (Onsite)
Full-Time
Monday to Friday, from 8:00 to 5:00, Mondays and Fridays remote
The Biocompatibility / Toxicology Expert will support the Biocompatibility Team to ensure the evaluation of biological safety and performance of *** Aesthetics Class III Absorbable Medical Devices for Aesthetics purpose (Dermal Fillers). She/he will be responsible for study design, planning, coordination and overseeing of her/his activities to support product development and life-cycle management in terms of biocompatibility and toxicology.
Major Duties & Description
1 Preparation of biological evaluation plan/report (BEP/BER) for projects/devices
Design preclinical programs to evaluate and demonstrate the safety and performance of medical devices in accordance with ISO standards and regulatory requirements (incl. but not limited to EU MDR, US FDA, Chinese Regulations) and internal quality procedures.
Preparation of Biological Evaluation Plan/Report and/or Biological Risk Assessments.
2 Maintenance of Non-Clinical Dossiers of Medical Devices
Cross-collaboration with Regulatory Affairs, Clinical team, and Production sites for the support to sustaining activities with regards to biocompatibility.
Maintenance activities include, but are not limited to, periodic update of BER, participate and review of Risk Management File (RMF)
3 Support to Production Sites (US and EU-based)
Prepare Biological Risk Assessments (BRA) in the frame of process changes on Legacy devices (incl. equipment, raw material, supplier changes etc.)
4 Management of preclinical biocompatibility studies
Planning, organization, monitoring and review of GLP biocompatibility (chemical and/or biological tests) studies with external laboratories
5 Ensure compliance with Regulatory standards/guidelines
Prepare Standard gap analyses and assess the impact(s) on current biocompatibility dossiers, studies and/or documentation
Technical & Functional Skills
Expertise in biocompatibility of Medical Devices
Knowledgeable about the biological evaluation standards, such as the ISO 10993 series
Fluency in English (French or German is a plus)
Knowledge of Microsoft Office Suite including Excel, Word, PowerPoint, Teams and SharePoint
Accurate, rigorous and clear communication (oral, written, face to face)
Very good scientific and analytical approach
Organized approach and able to work on multiple topics, with tight deadlines
Team Player, but able to work in autonomy
Minimum Qualifications
High scientific education such as biologist, biochemist, chemist (minimum BSc)
Biocompatibility Expert (former experience in biocompatibility assessment of medical devices > 12 months)
Medical Devices experience (> 3 years)
Travel Requirements
N/A
Physical Requirements
This position requires you to sit, stand and perform general office functions. You may also be required to lift up to twenty-five pounds occasionally. Bending, stooping and reaching are also frequently required.
Equal Employment Opportunity
It is our policy to provide equal employment opportunity for all applicants and colleagues. This policy includes our commitment to ensure that all employment decisions are made without regard to race, color, religion, gender, national origin, disability, pregnancy, veteran status (including Vietnam era veterans), age, sexual orientation, gender identity, or any other non-job-related characteristic protected by law.
The Biocompatibility / Toxicology Expert will support the Biocompatibility Team to ensure the evaluation of biological safety and performance of *** Aesthetics Class III Absorbable Medical Devices for Aesthetics purpose (Dermal Fillers). She/he will be responsible for study design, planning, coordination and overseeing of her/his activities to support product development and life-cycle management in terms of biocompatibility and toxicology.
Major Duties & Description
1 Preparation of biological evaluation plan/report (BEP/BER) for projects/devices
Design preclinical programs to evaluate and demonstrate the safety and performance of medical devices in accordance with ISO standards and regulatory requirements (incl. but not limited to EU MDR, US FDA, Chinese Regulations) and internal quality procedures.
Preparation of Biological Evaluation Plan/Report and/or Biological Risk Assessments.
2 Maintenance of Non-Clinical Dossiers of Medical Devices
Cross-collaboration with Regulatory Affairs, Clinical team, and Production sites for the support to sustaining activities with regards to biocompatibility.
Maintenance activities include, but are not limited to, periodic update of BER, participate and review of Risk Management File (RMF)
3 Support to Production Sites (US and EU-based)
Prepare Biological Risk Assessments (BRA) in the frame of process changes on Legacy devices (incl. equipment, raw material, supplier changes etc.)
4 Management of preclinical biocompatibility studies
Planning, organization, monitoring and review of GLP biocompatibility (chemical and/or biological tests) studies with external laboratories
5 Ensure compliance with Regulatory standards/guidelines
Prepare Standard gap analyses and assess the impact(s) on current biocompatibility dossiers, studies and/or documentation
Technical & Functional Skills
Expertise in biocompatibility of Medical Devices
Knowledgeable about the biological evaluation standards, such as the ISO 10993 series
Fluency in English (French or German is a plus)
Knowledge of Microsoft Office Suite including Excel, Word, PowerPoint, Teams and SharePoint
Accurate, rigorous and clear communication (oral, written, face to face)
Very good scientific and analytical approach
Organized approach and able to work on multiple topics, with tight deadlines
Team Player, but able to work in autonomy
Minimum Qualifications
High scientific education such as biologist, biochemist, chemist (minimum BSc)
Biocompatibility Expert (former experience in biocompatibility assessment of medical devices > 12 months)
Medical Devices experience (> 3 years)
Travel Requirements
N/A
Physical Requirements
This position requires you to sit, stand and perform general office functions. You may also be required to lift up to twenty-five pounds occasionally. Bending, stooping and reaching are also frequently required.
Equal Employment Opportunity
It is our policy to provide equal employment opportunity for all applicants and colleagues. This policy includes our commitment to ensure that all employment decisions are made without regard to race, color, religion, gender, national origin, disability, pregnancy, veteran status (including Vietnam era veterans), age, sexual orientation, gender identity, or any other non-job-related characteristic protected by law.
Get job alerts by email.
Sign up now!
Join Our Talent Network!