Princeton, New Jersey Hybrid Employment $90,000 to $105,000

Kyowa Kirin is hiring a Bioanalytical Specialist, Translational Research

About the Role

The Bioanalytical Specialist will be responsible for developing and validating bioanalytical methods, analyzing samples, and ensuring data integrity in a translational research setting.

Responsibilities

  • Develop and validate bioanalytical methods for various molecules.
  • Analyze samples using validated methods and ensure data integrity.
  • Collaborate with cross-functional teams to support research projects.
  • Maintain and troubleshoot laboratory equipment and instruments.
  • Document and report results accurately and in a timely manner.
  • Ensure compliance with regulatory guidelines and standard operating procedures.
  • Participate in the training and mentoring of junior staff.
  • Contribute to the development of new analytical techniques and methodologies.
  • Support the preparation of regulatory submissions and reports.
  • Conduct literature reviews and stay updated with industry trends and advancements.
  • Perform data analysis and interpretation to support research findings.
  • Assist in the design and execution of preclinical and clinical studies.
  • Collaborate with external partners and vendors as needed.
  • Participate in the review and approval of study protocols and reports.
  • Ensure the accuracy and reliability of analytical data.
  • Maintain a clean and organized laboratory environment.
  • Support the development of standard operating procedures and guidelines.
  • Contribute to the development of new analytical methods and techniques.
  • Participate in the review and approval of analytical methods and protocols.
  • Ensure the accuracy and reliability of analytical data.
  • Support the development of new analytical methods and techniques.
  • Participate in the review and approval of analytical methods and protocols.
  • Ensure the accuracy and reliability of analytical data.

Nice to Have

  • Experience in a pharmaceutical or biotechnology setting.
  • Familiarity with translational research methodologies.
  • Knowledge of bioanalytical software and tools.
  • Experience with regulatory submissions and reporting.
  • Ability to work independently and manage multiple tasks.
  • Experience with preclinical and clinical study design and execution.
  • Familiarity with laboratory equipment and instrumentation.
  • Strong problem-solving and troubleshooting skills.
  • Ability to maintain accurate and detailed records.
  • Experience with training and mentoring junior staff.
  • Knowledge of industry trends and advancements.
  • Ability to work in a fast-paced and dynamic environment.
  • Experience with cross-functional team collaboration.
  • Ability to ensure data integrity and compliance.
  • Experience with sample analysis and method validation.
  • Familiarity with standard operating procedures and guidelines.
  • Ability to contribute to the development of new analytical techniques.
  • Experience with literature reviews and industry research.
  • Ability to support the preparation of regulatory submissions and reports.
  • Experience with preclinical and clinical study design and execution.
  • Ability to collaborate with external partners and vendors.

Compensation

Competitive salary and benefits package

Work Arrangement

On-site, Full-time

Team

Collaborative and dynamic research team

Education

PhD in Analytical Chemistry, Bioanalytical Chemistry, or a related field.

Experience

  • Proven experience in bioanalytical method development and validation.
  • Experience in a pharmaceutical or biotechnology setting.
  • Experience with preclinical and clinical study design and execution.
  • Experience with regulatory submissions and reporting.
  • Experience with sample analysis and method validation.
  • Experience with training and mentoring junior staff.
  • Experience with cross-functional team collaboration.
  • Experience with literature reviews and industry research.
  • Experience with collaborating with external partners and vendors.

Skills

  • Expertise in LC-MS/MS and other analytical techniques.
  • Strong knowledge of regulatory guidelines and industry standards.
  • Experience with data analysis and interpretation.
  • Excellent communication and teamwork skills.
  • Ability to work independently and manage multiple tasks.
  • Strong problem-solving and troubleshooting skills.
  • Ability to maintain accurate and detailed records.
  • Familiarity with laboratory equipment and instrumentation.
  • Knowledge of industry trends and advancements.
  • Ability to work in a fast-paced and dynamic environment.
  • Ability to ensure data integrity and compliance.
  • Familiarity with standard operating procedures and guidelines.
  • Ability to contribute to the development of new analytical techniques.
  • Ability to support the preparation of regulatory submissions and reports.

Visa sponsorship available for eligible candidates

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About company
Kyowa Kirin
Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease. A Japan-based company, our goal is to translate science into smiles by delivering therapies where no adequate treatments currently exist, working from drug discovery to product development and commercialization. In North America, we are headquartered in Princeton, NJ, with offices in California, North Carolina, and Mississauga, Ontario.
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Job Details
Department Translational Research
Category other
Posted 2 hours ago