Aizant

Scientist - Analytical Development (Injectables)

Aizant

Hyderabad, Telangana, India · Full Time

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Experience
2–4 yrs
Salary
Openings
1
Posted
منذ 7 ساعات
Work mode
In office
Resume
Required to apply

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Job description

About Aizant Drug Research Solutions

Aizant Drug Research Solutions Private Limited is a comprehensive provider of drug development services. Established by pharmaceutical experts with global experience, the company is a fast-growing formulation CDMO and CRO catering to health care enterprises engaged in new molecular entities, generics, and OTC products worldwide. Aizant enhances client R&D throughout drug development stages from molecule discovery to commercialization and product lifecycle management, serving as the essential bridge between pharmaceutical firms and the healthcare sector.

Job Overview

We are looking for a driven and skilled Analytical R&D Scientist specializing in injectables to enhance our innovative team in Hyderabad (Dulapally). Candidates with 2-4 years of experience in analytical development will play a key role in creating improved formulations, verifying product quality, and ensuring regulatory compliance.

Primary Responsibilities

  • Adhere strictly to departmental Standard Operating Procedures (SOPs).
  • Maintain accurate, error-free, and real-time documentation of activities.
  • Ensure all analyses are conducted using calibrated instruments and equipment only.
  • Collaborate with supervisors to develop analytical methods for dissolution, assay via UV/HPLC, and related substances by HPLC.
  • Assist in method development for advanced techniques including peptide mapping and sequencing, circular dichroism spectroscopy, fluorescence spectroscopy, SEC-GPC/MALS, NMR, and comparative peptide/protein studies.
  • Carry out analysis of development samples according to test methods for dissolution, assay by UV/HPLC, and related substances by HPLC.
  • Validate test procedures such as dissolution, assay, related substances, residue, and chiral purity.
  • Ensure cleanliness of instruments and equipment post-analysis.
  • Manage receipt and proper storage of samples and standards.
  • Label standards, chemicals, and reagents accurately.
  • Receive log books and SOPs from Quality Assurance.
  • Ensure Good Laboratory Practice (GLP) compliance within the laboratory.
  • Support installation and commissioning of instruments and equipment.
  • Maintain reference and working standards and impurities adhering to GLP norms.
  • Archive completed files and Laboratory Notebooks (LNBs) efficiently.
  • Conduct analysis for water content using Karl Fischer titration, Loss on Drying (LOD), and identification tests per test methods and standards.
  • Coordinate and assist with timely calibration and preventive maintenance of instruments.

Additional Information

Immediate joiners will be given preference. Interested candidates are encouraged to apply promptly.

Industry

Pharmaceuticals

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