Aizant® is an integrated drug development solutions provider. Aizant was established by experienced pharmaceutical professionals with global exposure. We are a rapidly growing formulation CDMO and CRO with a diverse portfolio of capabilities partnering with health care companies specializing in new molecular entities (NME’s), generics (ANDA’s) and over the counter (OTC’s) products globally.

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We add exponential value to our client’s R&D programs at every stage of drug development right from the discovery of the molecule to commercialization and subsequent life cycle management. We are the vital link between the pharmaceutical companies and the healthcare industry.

We are a contract research organization (CRO) offering integrated drug development solutions including but not limited to product development, analytical development, bioanalytics, clinical, and diagnostics.

We are looking for young dynamic people who are committed to forming a perfect union between clinical care and research endeavors.

We are actively looking for people who are aggressive, willing to learn, contribute, and grow with the organization. Candidates with the following background are encouraged to apply. The candidates should have excellent academics with good communication and writing skills.

Position: Asst Manager – Analytical Method Validations

Location: Kompally, Hyderabad, Telangana

Job Description:

  • Review of departmental standard operating procedures (SOP) and Analytical test methods as per the requirement.
  • To ensure error-free and online documentation.
  • To ensure only the calibrated instruments/equipment are used for analysis.
  • Method development and validation as per the STP
  • To ensure that the analysis is done as per the STP
  • Review of analytical data and releasing the reports.
  • Review of analytical method validation, verification protocols, and reports.
  • Review of analytical method transfer products and reports
  • To ensure calibration of laboratory instruments/equipment as per the given schedule.
  • Carrying out laboratory investigation and literature search for any given product.
  • To report the Incident/deviation/event as per the SOP.
  • To ensure that the HPLC/GC columns are used and maintained properly as per the GLP.

  • Troubleshooting in the laboratory.
  • Participating in internal/sponsor/client auditing.
  • Review of analytical documents like SOP and Guidelines etc.
  • To ensure the dissolution, assay, and RS by UV/HPLC analysis is conducted as per the testing procedure.
  • Perform validation of test procedures like Dissolution, Assay, Related substances, Residue, and Chiral purity, etc.,
  • To ensure the GLP compliance in the laboratory.
  • To ensure the working standards, reference standards, and impurities are maintained as per GLP.
  • Any other work allotted by the supervisor.
  • Looking for Immediate joiners & worked with pharmaceutical companies.

Qualification: M.Pharma

Experience: 6-8 Years

Salary: Negotiable

Contact Details: 

Mr. Ambesh

ambesh.battula@aizant.com, hr@aizant.com  

web: https://www.aizant.com

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