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Japanese Speaking Jobs in Riverside, CA (NOW HIRING)

Experience in dealing with international tax matters a plusFluent in French(Francais), German(Deutsch), Japanese() or Mandarin() to include but not limited to speaking, writing and reading with a ...

Experience in dealing with international tax matters a plus Fluent in French(Francais), German(Deutsch), Japanese(日本語) or Mandarin(普通话) to include but not limited to speaking, writing and ...

Ability to additionally speak and write in Japanese and/or Spanish preferred. Work Environment: The work environment characteristics described here are representative of those an employee encounters ...

Tax Manager - Corporations

Irvine, CA · On-site

$119K - $156K/yr

Fluent in French(Francais), German(Deutsch), Japanese() or Mandarin() to include but not limited to speaking, writing and reading with a deep understanding of the culture and business practices ...

Server - PT

Riverside, CA · On-site

$17/hr

And it's all powered by Yoi Shigoto, a Japanese concept that translates to "good, quality work." It ... to speak, write, understand, and read English - Ability to operate standard serving equipment ...

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Japanese Speaking information

See Riverside, CA salary details

$13

$26

$42

How much do japanese speaking jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for japanese speaking in Riverside, CA is $26.76, according to ZipRecruiter salary data. Most workers in this role earn between $22.07 and $29.09 per hour, depending on experience, location, and employer.

What is a Japanese Speaking job?

A Japanese Speaking job requires proficiency in the Japanese language for communication, translation, or support tasks. These roles are common in customer service, translation, teaching, and corporate environments where interaction with Japanese-speaking clients, employees, or partners is necessary. Depending on the role, additional skills such as cultural knowledge or industry-specific expertise may be required.

What are the key skills and qualifications needed to thrive in the Japanese Speaking position, and why are they important?

To excel as a Japanese Speaking professional, fluent Japanese language skills, strong reading and writing abilities, and often at least a bachelor’s degree are essential. Familiarity with translation software, customer relationship management (CRM) systems, or industry-specific tools may be required, along with certifications such as JLPT (Japanese Language Proficiency Test). Excellent interpersonal skills, cultural awareness, and adaptability help candidates effectively bridge language and communication gaps. These qualifications ensure clear, accurate communication and successful collaboration between Japanese-speaking clients or partners and the team.

What types of tasks can I expect as a Japanese Speaking professional in a typical workday?

As a Japanese Speaking professional, your daily responsibilities may include translating documents, interpreting during meetings or conference calls, and assisting with written and verbal communication between Japanese and non-Japanese colleagues or clients. You might also support cross-department projects, facilitate negotiations, and provide cultural insights to ensure smooth business interactions. Depending on the industry and company, you could work closely with sales, customer support, or technical teams. Your role is vital in helping the organization build strong international relationships and deliver services to Japanese-speaking stakeholders.

What job categories do people searching Japanese Speaking jobs in Riverside, CA look for? The top searched job categories for Japanese Speaking jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Japanese Speaking jobs? Cities near Riverside, CA with the most Japanese Speaking job openings:
Associate Specialist - Premarket Regulatory Affairs

Associate Specialist - Premarket Regulatory Affairs

Applied Medical

Rancho Santa Margarita, CA • On-site

$70K - $80K/yr

Full-time

Medical, Life, Retirement, PTO

Posted 14 days ago


Applied Medical rating

8.3

Company rating: 8.3 out of 10

Based on 20 frontline employees who took The Breakroom Quiz


Job description

Applied Medical is a new-generation medical device company with a proven business model and commitment to innovation fueled by rapid business growth and expansion. Our company has been developing and manufacturing advanced surgical technologies for over 35 years and has earned a strong reputation for excellence in the healthcare field. Our unique business model, combined with our dedication to delivering the highest quality products, enables team members to contribute to a larger capacity than is possible in typical positions.


Position Description

Join Applied Medical as an Associate Specialist in Premarket Regulatory Affairs and help shape the future of medical innovation. You will be 100% on site, collaborating closely with cross-functional teams to support product development while ensuring alignment with regulatory standards. Your contributions will be key to maintaining and enhancing our Quality Systems, driving compliance from the earliest stages. This is your opportunity to make a meaningful impact on healthcare by helping bring safe, effective medical devices to market.

AREAS OF RESPONSIBILITY

The associate specialist is responsible for contributing to regulatory strategy and submission, participating in projects to maintain and improve the Quality Systems and ensuring that Applied Medical's Quality Systems conforms to standards and regulations in regions where Applied Medical products are distributed. The team member must be capable of working within a team environment, striving to meet customer expectations, and committing to continuous improvements in quality.

REGULATORY AND QUALITY PROJECT MANAGEMENT

Contribute to regulatory submissions, and projects for maintaining and improving the Quality System. Engage in regulatory strategy planning and change management for various markets, including Asia Pacific, Latin America, the European Union, and MENAT (Middle East North Africa). Represent Regulatory Affairs in decision-making and interdepartmental meetings related to domestic and international regulations.

COMMUNICATION

Collaborate with Engineering, Clinical Development, and global regulatory teams to meet regulatory requirements in markets where devices are distributed. Seek guidance and feedback from higher-level authorities, such as the Specialist, Senior Specialist, Manager, Director, or Vice President of Regulatory Affairs, and other teams.

PROBLEM SOLVING

Generate, review, and approve regulatory documentation, including assessments of regulatory actions, declarations of conformity, technical file summaries, and product labeling. Monitor the regulatory environment, keep current on relevant domestic and international standards, regulations, and guidance documents, and implement procedural updates and training to ensure conformance. Consider multiple pathways to compliance and incorporate diverse perspectives when creating solutions.


Position Requirements

This position requires the following skills and attributes:

  • At least one year of experience in Regulatory Affairs or Quality Assurance in the medical device industry
  • Proficient in interpreting regulations and standards
  • Highly motivated, self-starter, able to work independently and as part of a team
  • Strong analytical, detail-oriented, proactive mindset, not afraid to ask questions
  • Effective oral and written communication and presentation skills
  • Friendly, positive attitude, committed to excellent customer service
  • Exemplary time and resource management skills, able to multitask, organize, and prioritize
  • Strong technical writing skills
  • Committed to quality and continuous improvement, strives to meet, or exceed customer expectations

Preferred

The following skills and attributes are preferred:

  • Bachelor's degree in Engineering, Physical or Biological Sciences, Regulatory, other technical disciplines, or an equivalent field of study
  • Training in Quality Systems, including Quality Systems Regulations (QSRs) and Good Manufacturing Practices (GMPs) for medical devices, and International Organization for Standardization (ISO) standards
  • Proficiency in speaking and writing in Japanese or Korean is preferred

If you are excited about making a significant impact, driving innovation, and contributing to a dynamic team, we encourage you to apply and embark on an exciting journey of engineering excellence at Applied Medical. Our unique business model empowers our team members to have a substantial impact, unlike conventional roles.


Benefits
  • Competitive compensation range: $70000 - $80000 / year (California).
  • Comprehensive benefits package.
  • Training and mentorship opportunities.
  • On-campus wellness activities.
  • Education reimbursement program.
  • 401(k) program with discretionary employer match.
  • Generous vacation accrual and paid holiday schedule.

Please note that the compensation range may be based on factors such as relevant education, qualifications, experience. The compensation range may be adjusted in the future, and special discretionary bonus or incentive compensation plans may apply.

Our total reward package reflects our commitment to team member growth and well-being, as we invest in your development and offer a range of benefits designed to enhance your career and life.

Equal Opportunity Employer

Applied Medical is an Equal Employment Opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (including pregnancy, childbirth, breastfeeding and related medical conditions), or sexual orientation, or any other basis protected by federal, state or local laws in the locations where Applied Medical operates. 

Qualifications:

This position requires the following skills and attributes:

  • At least one year of experience in Regulatory Affairs or Quality Assurance in the medical device industry
  • Proficient in interpreting regulations and standards
  • Highly motivated, self-starter, able to work independently and as part of a team
  • Strong analytical, detail-oriented, proactive mindset, not afraid to ask questions
  • Effective oral and written communication and presentation skills
  • Friendly, positive attitude, committed to excellent customer service
  • Exemplary time and resource management skills, able to multitask, organize, and prioritize
  • Strong technical writing skills
  • Committed to quality and continuous improvement, strives to meet, or exceed customer expectations
Education:UNAVAILABLEEmployment Type: FULL_TIME

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