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Etico Lifesciences Hiring 2025 for Analytical Research & Development Jobs in Hyderabad

Etico Lifesciences Pvt. Ltd., a USFDA-registered (FEI No: 3013758337, DUNS No: 67-546-6037) and ISO 9001:2015-certified pharmaceutical product development company, is seeking talented professionals for Analytical Research & Development (AR&D) roles at its R&D facility in Pragati Nagar, Hyderabad.

Founded in 2016, Etico specializes in niche generic and specialty parenteral and ophthalmic formulations, applying Quality by Design (QbD) principles to ensure robust product development and successful technology transfer [Web:3,7]. Join our dynamic team to drive innovation in solid dosage, injectable, ophthalmic, and semi-solid formulations!

Note: Etico Lifesciences does not charge any fees for job applications. Beware of fraudulent invitations requesting payment; contact careers@eticolifesciences.com for verification.

Job Details

  • Department: Analytical Research & Development (AR&D)
  • Position: Executive / Senior Executive (based on experience)
  • Experience: 3–5 Years in analytical R&D for pharmaceutical formulations
  • Qualification: B.Pharm / M.Pharm / M.Sc (Chemistry, Analytical Chemistry, Pharmaceutical Sciences)
  • Location: Etico Lifesciences Pvt. Ltd., Plot No. 64 & 70, Flat No. 6A, Rohith Residency, Pragati Nagar, Hyderabad, Telangana – 500090

Job Description:

  • Develop and validate analytical methods for solid dosage forms, injectables, ophthalmic, and semi-solid formulations per ICH guidelines [Web:0,1,3].
  • Operate and maintain analytical instruments, including HPLC, GC, Karl Fischer (KF), and UV-Vis spectrophotometer, for routine and specialized testing.
  • Execute analytical parameters such as Assay, Related Substances, Dissolution, and Residual Solvents testing.
  • Conduct Analytical Method Validation (AMV), Analytical Method Transfer (AMT), and stability testing (accelerated, long-term) in compliance with GLP and regulatory standards (USFDA, ICH).
  • Prepare technical documentation (e.g., method development reports, validation protocols, stability study reports) and support regulatory audits.

Key Skills:

  • Hands-on expertise in HPLC, GC, KF, and UV for formulation analysis [Web:1,7].
  • Strong knowledge of AMV, AMT, stability testing, and GLP practices.
  • Ability to design experiments, analyze lab data, and draw actionable conclusions.
  • Familiarity with chromatography software (e.g., Empower, Chromeleon) and QbD principles.
  • Excellent documentation and communication skills for regulatory compliance.
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Why Join Etico Lifesciences?

  • Innovative Leader: Work with a research-driven company specializing in complex parenteral and ophthalmic formulations, including solutions, emulsions, suspensions, and lyophilized products.
  • Global Impact: Contribute to products developed for worldwide markets, backed by Etico’s USFDA registration and global partnerships.
  • Supportive Environment: Join a team of experienced scientists with a track record of successful project delivery from concept to commercialization.
  • Career Growth: Access training in advanced analytical techniques and opportunities to lead method development projects.
  • Benefits: Competitive salary (₹3.5–₹7 Lakhs for similar roles), health insurance, and performance-based incentives.

Learn more about our mission at Etico Lifesciences and industry standards at USFDA or ICH.

How to Apply

  1. Email Your Resume: Send your updated CV to careers@eticolifesciences.com with the subject “AR&D Application – [Your Name]” by June 10, 2025.
  2. Documents Required:
    • Updated CV highlighting relevant experience and skills.
    • Copies of educational certificates (B.Pharm/M.Pharm/M.Sc).
    • Last 3 months’ payslips and latest CTC document (if applicable).
  3. Selection Process:
    • Shortlisting based on CV and experience.
    • Technical interview (analytical method development, instrument handling, GLP knowledge).
    • HR interview (fit, salary expectations).
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The post is released by the Etico LifeScience LinkedIn page. Click here to visit the post

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