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Scientist I Immunoassay

Resolian

Malvern (Chester County)

On-site

USD 43,000 - 52,000

Full time

13 days ago

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Job summary

An established industry player is seeking a skilled Research Specialist to develop and validate bioanalytical methods. This role involves serving as the Principal Investigator and ensuring compliance with regulatory standards. You'll be responsible for maintaining high-quality results and client satisfaction through effective communication and mentorship of junior staff. Join a dynamic team that values scientific rigor and innovation in the biotechnology sector, where your expertise will contribute to meaningful advancements in research and development.

Qualifications

  • 7-8 years of lab experience required.
  • Knowledge of regulatory requirements is essential.

Responsibilities

  • Develop and troubleshoot bioanalytical methods for sample testing.
  • Maintain client satisfaction through timely communication.

Skills

Laboratory Experience
Regulatory Knowledge (GLP, GCP)
Complex Lab Work
Team Collaboration
Computer Systems Proficiency

Education

BA/BS or higher

Job description

Direct message the job poster from Resolian

  • Develop, validate, and troubleshoot bioanalytical methods (e.g., ELISA, MSD, qPCR/RT-qPCR, etc.) for sample testing and data reporting, serving as the Principal Investigator (PI) as required.
  • Present and interpret data both internally and externally, ensuring clarity and scientific rigor.
  • Maintain client satisfaction through timely communication, responsiveness, and on-schedule delivery of high-quality results.
  • Prepare and review laboratory data and controlled documents, including study plans and final reports.
  • Support laboratory operations and provide mentorship to junior staff members.
  • Contribute to the development and refinement of policies, procedures, work instructions, and standard operating procedures (SOPs).
  • Ensure compliance with company standards, including Code of Conduct, Environmental Health and Safety (EHS), and GLP/GCP/GDP regulations.
  • Perform additional duties as assigned to support team and organizational goals.

Skills, Education & Qualifications

  • BA/BS or higher with 7-8 years lab experience; all experiences will be evaluated
  • Knowledge and understanding of regulatory requirements; GLP, GCP, 21CFR Part 11, GDP, GMP
  • Able to independently perform complex lab work
  • Able to work in a regulated environment
  • Able to work effectively and contribute within a team
  • Able to work with computer systems
  • Knowledge of and experience in a regulatory environment
Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Research and Science
  • Industries
    Biotechnology Research and Research Services

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