Specialist, Regulatory Affairs

Reposted 17 Days Ago
Be an Early Applicant
Beijing, CHN
In-Office
Junior
Biotech
The Role
Responsible for product registration approval, strategy execution in multiple markets, maintaining documentation, and providing regulatory support across teams.
Summary Generated by Built In
FUNCTION: This position will have responsibility to:
  • Submit product registration dossier and get approval according to the registration plan, with compliance to regulations and SOP.

  • Execute product registration strategy plans in China/US/EU/Other target markets.

  • Follow up and interpret Global MD, IVD related regulation updates.

  • Establish and maintain good relationship with key contacts such as type testing centers, NMPA and its affiliated organizations.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

The incumbent will also be responsible for, but not limiting to the following duties:

  • Complete overseas registration cases and get product certificates according to registration plan.

  • Maintain submission documents and approval documents in related IT systems.

  • Provide the regulatory support to cross-functional team within and outside China.

  • Provide necessary support to dealers and customers for regulatory compliance.

  • Collect, analysis the new released regulations globally.

This description is a summary of principle responsibilities and is not intended to include all duties may be assigned.

WORKING RELATIONSHIPS AND CONTACTS:

  • External contacts for this position include NMPA officials / Overseas health authority officials, dealers and users/customers, local testing center,

  • Internal contacts include headquarter, marketing team, logistic team, application and sales/service team, QA, R&D.

ESSENTIAL QUALIFICATIONS:

EDUCATION & SKILLS:

  • Bachelor degree or above.

  • Medicine / bioengineering / clinical medicine / biochemistry or pharmacy relevant background is preferred.

  • Good English and Chinese language skills

WORKING EXPERIENCE:

This position requires:

  • 2 years or above RA working experience in IVD industry.

  • Preferably China MD and IVD registration experiences.

FUNCTIONAL COMPETENCIES:

  • Expertise in NMPA regulation of IVD and/or medical devices and in NMPA registration process;

  • Excellent teamwork and interpersonal communication skill;

  • Good attitude, positive thinking & take responsibility;

  • Creative thinking for complexed registration cases.

TRAVEL REQUIREMENTS:

This position may require business traveling in a fewness situation.

WORK ENVIRONMENT: 

This position functions in a general office environment. 

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

Skills Required

  • Bachelor degree or above
  • 2 years or above RA working experience in IVD industry
  • Good English and Chinese language skills
  • Expertise in NMPA regulation and registration process

Cepheid Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Cepheid and has not been reviewed or approved by Cepheid.

  • Leave & Time Off Breadth PTO and paid holidays are portrayed as robust, with formal programs and mentions of generous time off and rollover in some cases. This breadth supports a positive view of time-off availability.
  • Healthcare Strength Core medical, dental, and vision coverage is highlighted repeatedly and is viewed as comprehensive for regular full‑time employees. Descriptions such as “good” or “great” benefits reinforce the strength of the health coverage.
  • Retirement Support A 401(k) plan with company matching is consistently included as part of the package. The presence of matching contributions strengthens perceived retirement readiness.

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The Company
HQ: Sunnyvale, CA
4,883 Employees
Year Founded: 1996

What We Do

Cepheid is dedicated to improving healthcare by pioneering molecular diagnostics that combine speed, accuracy, and flexibility. The company's GeneXpert® systems and Xpert® tests automate highly complex and time-consuming manual procedures, providing A Better Way for institutions of any size to perform world-class PCR testing. Cepheid’s broad test portfolio spans respiratory infections, blood virology, women’s and sexual health, TB and emerging infectious diseases, healthcare-associated infectious diseases, oncology and human genetics. The company’s solutions deliver actionable results where they are needed most – from central laboratories and hospitals to near-patient settings. For more information, visit http://www.cepheid.com.

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