Scientific Research Lead for Medical Aesthetics
4 days ago
At Brunel, we are seeking an accomplished S cientific Research Lead for Medical Aesthetics to join our esteemed team. With a strong focus on product development and innovative research, this role offers an exceptional opportunity to contribute to the growth of a leading manufacturer of HA fillers worldwide.
The successful candidate will serve as a technical leader, overseeing research activities from project conception to monitoring, resource management, scientific data review, and reporting. This position reports directly to the Global Chief Scientific Officer.
This is a highly demanding yet rewarding role that requires expertise in medical device development, biologics, and regulatory standards (ISO). The ideal candidate will have a PhD in Chemistry, Materials Science, or Polymer Science with 10-12 years of related industrial experience.
The key responsibilities of this position include:
- Technical Leadership: Drive the execution of technical development plans spanning preclinical animal studies through process validation to support IDE and PMA submission.
- Project Initiation: Develop and implement new projects for the R&D team to ensure a consistent product pipeline.
- Data Review and Evaluation: Supervise project-related scientific/technical activities, contribute to strategic decision-making, and interpret results.
- Regulatory Compliance: Ensure technical readiness by designing, reviewing, and approving animal study protocols for preclinical studies in support of IDE submission.
- Technical Expertise: Author drug and medical device IDE and PMA modular components covering product background, device description, preclinical testing, product biocompatibility, manufacturing process, and product testing and characterization.
- Collaboration: Partner with Quality/Regulatory and Analytical Technical experts to prepare Technical Files and Design Dossiers in line with market requirements.
- Technology Evaluation: Assist the Global Chief Scientific Officer in evaluating key technologies of biotech companies and analyzing their technological capabilities for M&A activities.
- Budget Management: Assist the Global Chief Scientific Officer in evaluating budgetary proposals from Contract Manufacturing Organizations (CMOs) to determine the optimum budget for product characterization and biocompatibility studies.
- Team Collaboration: Be a key member of the R&D, Regulatory, and Clinical bi-weekly team meeting in preparation of IDE and PMA submissions.
- Communication: Communicate current scientific findings to the Global Chief Scientific Officer through peer-review journals, ISO standards, and clinical trials to assist in the company's product development pipeline.
We offer a competitive salary range of $150,000 - $180,000 per annum, commensurate with experience, plus benefits.
About Us
Brunel has a reputation for working with top talent across various industries. With over 45 years of experience, we've created a global network of clients and professionals working together through a wide range of services.
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