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Biotechnology Japan Jobs (NOW HIRING)

Quality Control Analyst I

Pittsburgh, PA · On-site

$23.25 - $31.25/hr

At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the ... and Japan. We are a company built and run by people who care, are fearless in the face of a ...

Quality Control Analyst I

Pittsburgh, PA · On-site

$23.25 - $31.25/hr

At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the ... and Japan. We are a company built and run by people who care, are fearless in the face of a ...

Lab Technician

Piscataway, NJ · On-site

$19 - $25.25/hr

Company Description GenScript Biotech Corporation is a leading Contract Research Organization and ... There are also branches in Ireland, Netherlands, and Japan. We have been serving more than 100 ...

Lab Technician

Piscataway, NJ

$19 - $25.25/hr

Company Description GenScript Biotech Corporation is a leading Contract Research Organization and ... There are also branches in Ireland, Netherlands, and Japan. We have been serving more than 100 ...

$60 - $80/hr

At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the ... and Japan. We are a company built and run by people who care, are fearless in the face of a ...

About Krystal Bio At Krystal Biotech, we bring together the brightest and most eager minds to ... and Japan. We are a company built and run by people who care, are fearless in the face of a ...

Senior Engineer, MSAT

Seattle, WA · On-site

$140K - $164K/yr

... Japan's PMDA. Aurion Biotech is the recipient of the prestigious Prix Galien award for best start-up in biotech. The Company is preparing for clinical trials in the U.S. We are growing rapidly and ...

Quality Coordinator

Seattle, WA · On-site

$72K - $79K/yr

... Japan's PMDA. Aurion Biotech is the recipient of the prestigious Prix Galien award for best start-up in biotech. The Company is preparing for clinical trials in the U.S. We are growing rapidly and ...

Showing results 21-40

Biotechnology Japan information

See salary details

$28.5K

$73.6K

$149.5K

How much do biotechnology japan jobs pay per year?

As of Sep 8, 2026, the average yearly pay for biotechnology japan in the United States is $73,591.00, according to ZipRecruiter salary data. Most workers in this role earn between $47,000.00 and $89,500.00 per year, depending on experience, location, and employer.

What is biotechnology in Japan?

Biotechnology in Japan refers to the use of biological processes, organisms, or systems to develop products and technologies that benefit society. In Japan, the biotechnology sector is known for its advancements in pharmaceuticals, medical devices, agriculture, and environmental solutions. The industry is supported by government initiatives, strong research institutions, and collaborations between academia and private companies. Japan is recognized for its innovation in fields like regenerative medicine, genetic engineering, and industrial biotechnology. The sector plays a crucial role in addressing healthcare challenges and supporting sustainable development.

What are the key skills and qualifications needed to thrive in the biotechnology industry in Japan?

To thrive in the biotechnology industry in Japan, you need a solid background in life sciences, molecular biology, and biochemistry, often supported by a relevant degree or advanced research experience. Familiarity with laboratory techniques, bioinformatics tools, and regulatory compliance systems—such as GLP/GMP standards—is typically required. Strong analytical thinking, cross-cultural communication, and adaptability set professionals apart in this rapidly evolving field. These skills and qualifications are crucial for driving innovation, ensuring product quality, and collaborating effectively in Japan's competitive biotech sector.

What are some common challenges faced by professionals working in biotechnology roles in Japan, and how can they be addressed?

Professionals in biotechnology roles in Japan often encounter challenges such as navigating strict regulatory requirements, adapting to rapidly evolving technologies, and collaborating across interdisciplinary teams. Language barriers and cultural differences can also impact communication, especially in international or joint-venture projects. Building strong cross-functional relationships, staying up-to-date with industry regulations, and proactively seeking professional development opportunities can help address these challenges and enhance career growth.

What is the difference between Biotechnology Japan vs Biomedical Scientist?

AspectBiotechnology JapanBiomedical Scientist
Required CredentialsDegree in Biotechnology, Life Sciences, or related fields; certifications varyDegree in Biomedical Science, Medicine, or related fields; certifications may include licensing
Work EnvironmentResearch labs, biotech companies, manufacturing facilitiesHospitals, research institutions, clinical labs
Employer & Industry UsageBiotech firms, pharmaceutical companies, research organizationsHealthcare providers, hospitals, academic research centers

Biotechnology Japan professionals focus on developing and manufacturing biotech products, while Biomedical Scientists primarily conduct medical research and support clinical diagnostics. Both roles require a strong background in life sciences but differ in work settings and specific responsibilities.

More about Biotechnology Japan jobs

What cities are hiring for Biotechnology Japan jobs?

Cities with the most Biotechnology Japan job openings:

What states have the most Biotechnology Japan jobs?

States with the most job openings for Biotechnology Japan jobs include:

Infographic showing various Biotechnology Japan job openings in the United States as of August 2026, with employment types broken down into 86% Full Time, 10% Part Time, 1% Temporary, and 3% Contract. Highlights an 70% Physical, 3% Hybrid, and 27% Remote job distribution, with an average salary of $73,591 per year, or $35.4 per hour.

Quality Assurance Associate

Krystal Biotech

Pittsburgh, PA • On-site

Full-time

Re-posted 10 days ago


Key responsibilities

  • Support quality systems and GMP manufacturing processes through documentation and oversight.

  • Review and approve manufacturing and quality control records to ensure compliance.

  • Assist with updates to standard operating procedures and GMP-related documentation.


Job description

About Krystal Bio:  
At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs.
Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient’s end-to-end experience.
Krystal received U.S. FDA approval for the first and only redosable gene therapy treatment, VYJUVEK®, for the treatment of Dystrophic Epidermolysis Bullosa (DEB). Krystal continues to leverage our proprietary platform to rapidly advance a robust pipeline of investigational genetic medicines in respiratory, oncology, dermatology, and ophthalmology.
Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP manufacturing facilities with teams around the world and satellite offices in Switzerland, Germany, and Japan. We are a company built and run by people who care, are fearless in the face of a challenge, love the work they do, and practice the highest level of scientific integrity. As we grow, we are seeking team members that embody these values.
Job Description Summary:
Krystal Biotech, Inc. is seeking a highly motivated and experienced Quality Associate to support quality systems, GMP manufacturing processes and documentation practices at our headquarters in Pittsburgh's South Side.  
Primary Responsibilities:
  • Work with internal teams to obtain an understanding of the product and the documentation requirements.
  • Produce high-quality documentation that meets applicable standards and is appropriate for its intended use.
  • Develop expertise on FDA regulations and audit processes.  
  • Initiate and update GMP manufacturing associated documentation, such as clearing procedures.
  • Provide oversight of daily QA functions which include review and approval of records generated by manufacturing and quality control documents.
  • Provide support for updates on standard operating procedures and associated forms.
  • Assist with QA efforts for site cGXP documentation related to the operation of gene therapy manufacturing.
  • Ensure compliance with regulatory agencies and oversee continuous improvement of company's QA and compliance functions.
Requirements & Desired Competencies:
  • Minimum of a Bachelor’s Degree (Biology or related Life Science) with 3+ years of relevant quality systems experience in the biotech or pharmaceutical industry.
  • Background that includes knowledge/experience in GMP, GLP, and GCP.
  • Experience with FDA audits is highly preferred.
  • Strong knowledge of GMP and ICH requirements.
  • Must be a self-starter and capable of working with minimal oversight.
  • Must be able to handle multiple roles and work in a fast paced and changing environment and know how to prioritize activities appropriately.
  • Excellent oral and written communication skills.

Krystal Biotech, Inc. is an Equal Employment Opportunity and Affirmative Action Employers. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. Headhunters and recruitment agencies may not submit resumes/CVs through this Web site or directly to managers. Krystal Biotech, Inc. does not accept unsolicited headhunter and agency resumes. Krystal Biotech, Inc.  will not pay fees to any third-party agency or company that does not have a signed agreement with Krystal Biotech, Inc. 
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