R&D Manager - Bilingual (Mandarin Speaking)
Posted Updated
Description
Description
CorDx, a fast-growing biotech company, is seeking a highly qualified R&D Manager to lead the development and implementation of innovative products and services. The ideal candidate will have a strong background in biotechnology and a passion for pioneering new solutions in the field. This position offers the opportunity to work with a dynamic team and make a significant impact on the company's growth trajectory.
Responsibilities
- Develop and implement cutting-edge R&D strategies to create new products and enhance existing ones.
- Lead a team of research and development professionals through the entire product development lifecycle.
- Oversee the design, execution, and analysis of experiments, including the preparation of technical reports and presentations.
- Establish and maintain partnerships with academic and industry research organizations.
- Collaborate with cross-functional teams, including marketing and regulatory, to ensure that products meet customer needs, quality standards, and regulatory requirements.
- Serve as a technical expert, providing guidance and support to internal and external stakeholders.
- Stay current with the latest trends and innovations in biotechnology and related fields.
Requirements
- PhD in Biotechnology, Bioengineering, or a related field.
- At least 5 years of industry experience in R&D management.
- Proven track record of success in developing and commercializing innovative products.
- Strong leadership and team management skills.
- Excellent written and verbal communication skills.
- Ability to work independently and collaboratively.
- Experience with project management tools and software.
- Mandarin speaking is preferred
Benefits
- Health Care Plan (Medical)
- Paid Time Off
- Training & Development
As published by workable · 12 questions
Basics
First name, Last name, Email, Phone, Address, Resume
Short answers (2)
- How many projects have you supported that required FDA compliance or regulatory oversight?
- What is your expected salary range for this role?
Pick from a list (10)
- Would you be able to work 5 days onsite in Alpharetta, GA office location?
- Do you have experience working under ISO 13485 quality management systems?
- Have you participated in FDA inspections, audits, or regulatory submissions?
- Do you have experience with Class I, II, or III medical devices?
- Have you worked with point-of-care diagnostic devices?
- Are you familiar with ISO 9001 processes in an R&D or lab environment?
- Will you now, or in the future, require sponsorship for employment visa status (e.g. H-1B visa status)?
- Do you have hands-on experience developing lateral flow assays (LFAs)?
- Have you been involved in preparing or submitting documentation to the FDA for device approval or clearance?
- Are you fluent in Mandarin Chinese?
