Lead Biaassay | Dr Reddys Labs | Visakhapatnam, Hyderabad

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Job Overview

  • Date Posted
    November 13, 2022
  • Location (State / UT)
  • Expiration date
    --
  • Experience
    18 Years, 20 Years
  • Gender
    Any
  • Desired Qualification
    Master’s Degree, Doctorate Degree

Job Description

  • Develop, Optimize and successfully implement in silico, innate, and adaptive immunogenicity studies with in-depth knowledge of handling the generic molecules across the agencies.
  • Develop, optimize and successfully implement robust analytical methods for in vitro biochemical assays, and cell-based assays. In-depth knowledge in recombinant proteins and peptide molecules, binding assays, quantitative assays using spectrophotometric tools, enzyme kinetic methods, ELISA, etc.
  • Expertise in handling Flow cytometry and Luminex platform (xMAP Technology) is a key requirement.
  • Conduct a literature search, review, and study relevant literature based on the work assigned. Maintain and develop scientific knowledge and skills as required to complete work and stay current on scientific trends and developments related to the responsibilities.
  • Perform day-to-day analysis of samples and support product development. Analyze the in-process samples, developmental batches, and stability samples (API & DP). Work for any deficiency response on high priority. Conduct method validations and method transfers.
  • Identify critical reagents & reference standards for any new method, procure and maintain them as per the stability & storage protocols. Maintain consumable usage log. Procure reagents, chemicals, solvents, plates, microfuge tubes, tips, and other consumables.
  • Follow proper and online documentation procedures as per cGLP. Prepare SOPs, STPs, study reports, and other documents as required. Prepare method development and method validation protocols and reports. Prepare stability data reports.
  • Investigate abnormal results and take initiative with the group leader by raising, discussing, and resolving matters and issues.
  • Check the performance of the analytical instruments in order to ensure regular analysis and regular calibration of instruments as per the SOPs. Prepare buffers, reagents, and other requirements for day-to-day assay performance.
  • Adhere to the product delivery timelines and quality standards. Understand and follow the safety and environmental regulations of the company.
  • Follow general practices of handling cell cultures, proteins, peptides & other bio-molecules.
  • Adhere to the product delivery timelines and quality standards. Understand and follow the safety and environmental regulations of the company.

Education & Experience:

Ph D. Biotechnology / Biochemistry / Immunology or any other relevant field of Life Sciences with 12-18 years of industrial experience with developing, Optimize, and successfully implementing in silico, innate and adaptive immunogenicity studies with in-depth knowledge on handling generic molecules across the agencies