Japan/South Korea(remote) This role required to work in Japan or South Korea Are you a ... packaging and microbiological testing outlined under ISO 13485. In this role you will have the ...
Japan/South Korea(remote) This role required to work in Japan or South Korea Are you a ... packaging and microbiological testing outlined under ISO 13485. In this role you will have the ...
Japan/South Korea(remote) This role required to work in Japan or South Korea Are you a ... packaging and microbiological testing outlined under ISO 13485. In this role you will have the ...
Japan/South Korea(remote) This role required to work in Japan or South Korea Are you a ... packaging and microbiological testing outlined under ISO 13485. In this role you will have the ...
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Remote Packaging Development information
What are the key skills and qualifications needed to thrive as a Remote Packaging Development Specialist, and why are they important?
What is the difference between Remote Packaging Development vs Remote Packaging Technician?
| Aspect | Remote Packaging Development | Remote Packaging Technician |
|---|---|---|
| Credentials | Degree in Packaging Engineering or related field, certifications like CPP or PMP often preferred | Technical diploma or certification in packaging technology or related area |
| Work Environment | Design, planning, and development in office or remote settings, collaboration with R&D teams | Implementation, troubleshooting, and quality checks, often in production or warehouse settings |
| Industry Usage | Used across manufacturing, consumer goods, and logistics companies for new product packaging | Common in manufacturing plants, warehouses, and distribution centers |
Remote Packaging Development focuses on designing and planning packaging solutions, requiring engineering knowledge and collaboration with R&D teams. In contrast, Remote Packaging Technician handles the implementation, troubleshooting, and quality assurance of packaging processes, often in production environments. Both roles are essential in the packaging industry but differ in responsibilities, skills, and work settings.
What is remote packaging development?
What are some common challenges faced by professionals in Remote Packaging Development roles, and how are they typically addressed?
Other
Re-posted 3 days ago
Job description
We exist to create positive change for people and the planet. Join us and make a difference too!
Job title: Technical Specialist and Scheme Manager (Microbiology)-relocation acceptable
Location: Japan/South Korea(remote)
This role required to work in Japan or South Korea
Are you a Microbiologist, Sterilization Engineer, or Quality Manager looking for an interesting career change?
BSI hires qualified and experienced industry microbiologists to help clients navigate the areas of compliance within the areas of sterilization, packaging and microbiological testing outlined under ISO 13485. In this role you will have the opportunity to apply your sterile medical device experience to impact patient safety and help determine which new products go to market.
Technical Specialist Responsibilities:
Responsible for planning, reporting and performing of audits of clients' management systems ensuring compliance with regulatory and voluntary requirements.
Conduct comprehensive in-depth medical device reviews (including sterilization validation).
Make recommendation whether to issue a certificate, based on objective evidence that the device is safe and effective.
The Technical Specialist - Microbiology role requires maturity to make difficult decisions regarding the benefits and risks of medical device products and whether to recommend certification. The individual must be able to clearly and confidently communicate with clients. Please carefully review the qualifications listed below and apply if you meet the criteria.
Education/Qualifications:
- A minimum of four (4) years' experience working as a microbiologist and/or sterilization engineer for asterile medical device manufacturer
- Bachelor's degree (or higher) in Microbiology, Biology or related scientific degree
- Familiar with Gamma and EO sterilization
- Thorough knowledge of ISO 13485 quality standard and familiarity with Medical Devices Directive (MDD)/EU Medical Device Regulation (MDR)
- Quality management experience including significant participation in third party quality audits
- If you apply the role in Japan, then Native Japanese speaking required.
- If you apply the role in South Korea then Native Korean speaking required.
About Us
BSI is a business improvement and standards company and for over a century BSI has been recognized for having a positive impact on organizations and society, building trust and enhancing lives.
Today BSI partners with more than 77,500 clients in 195 countries and engages with a 15,000 strong global community of experts, industry and consumer groups, organizations and governments.
Utilizing its extensive expertise in key industry sectors - including automotive, aerospace, built environment, food and retail, and healthcare - BSI delivers on its purpose by helping its clients fulfil theirs.
Living by our core values of Client-Centricity, Agility, and Collaboration, BSI provides organizations with the confidence to grow by partnering with them to tackle society's critical issues - from climate change to building trust in digital transformation and everything in between - to accelerate progress towards a better society and a sustainable world.
BSI is an Equal Opportunity Employer dedicated to fostering a diverse and inclusive workplace.