Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Ivd Elisa - R&D (Executive)

Promea
Promea
1-2 years
Not Disclosed
10 Feb. 10, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: IVD ELISA - R&D Executive
Experience: 1-2 years
Location: Hyderabad
Employment Type: Full-Time


Job Summary:

We are seeking a highly motivated R&D Associate with 1 to 2 years of hands-on experience in ELISA development and assay optimization. The ideal candidate will be responsible for developing, optimizing, and validating ELISA-based assays for both research and product development purposes. This is a great opportunity to work in a fast-paced environment within a cross-functional team to develop innovative solutions for diagnostic and therapeutic applications.


Key Responsibilities:

  1. R&D Management:

    • Manage the activities of a group focused on research and development for diagnostic product markets.
  2. Project Execution:

    • Execute all project tasks, ensuring that work and reports meet project milestones and objectives.
  3. Experimental Design:

    • Design and execute experiments to ensure that they are appropriate and effective for project needs.
  4. Protocol and Report Preparation:

    • Prepare detailed protocols and reports, ensuring that all project objectives and requirements are met.
  5. Technical Documentation:

    • Draft and edit technical documents such as technical reports, design documents, and QC specifications to support the R&D process.
  6. Validation and Verification:

    • Perform validation and verification activities for developed products to ensure compliance with quality standards.
  7. Rapid Kit Optimization:

    • Optimize and formulate rapid diagnostic kits for improved performance and efficiency.
  8. Ad-hoc Tasks:

    • Take on any additional work assigned by the reporting head as necessary to support the team and R&D initiatives.

Key Skills & Qualifications:

  • Educational Qualification:

    • Bachelor’s or Master’s degree in Biotechnology, Life Sciences, or a related field.
  • Experience:

    • 1-2 years of hands-on experience in ELISA development, assay optimization, and product validation.
  • Skills & Competencies:

    • Strong understanding of ELISA-based assay development and optimization.
    • Experience in product validation and verification processes.
    • Ability to manage and execute R&D projects to meet milestones.
    • Familiarity with technical documentation, including report writing and protocol creation.
    • Strong problem-solving skills and attention to detail.
    • Ability to work effectively in a team environment.

This position offers the opportunity to work at the forefront of diagnostic innovation while contributing to meaningful projects in healthcare. If you are an enthusiastic individual with a strong background in ELISA development and optimization, we encourage you to apply!