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Senior Executive/Executive Quality Control | Aizant Drug Research | Hyderabad | 2.00-4.00 L


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: Sr Executive – Quality Control

Location: Kompally, Hyderabad, Telangana, India

Job Description:

Roles and Responsibilities

  • Collection of water samples for analysis and analyze water samples for chemical analysis.
  • To sample, analyze, review of Raw materials and packaging materials.
  • Preparation of Certificate of Analysis (COA) for water samples, Raw materials, and packaging materials.
  • To analyze and release of In-process and Finished products
  • Preparation and Analytical reports for In-process, finished products, and stability samples.
  • To report the incident as per the SOP.
  • Participating in internal / sponsor / client auditing.
  • To ensure calibration of laboratory instruments/equipment as per the given schedule.
  • Daily temperature and humidity monitoring of the QC laboratory.
  • Receiving logbooks, SOP’s from QA
  • Labeling of standards, chemicals, and reagents.
  • To ensure that the HPLC/GC Columns are used and maintained properly as per GLP.
  • Preparation of Record Analysis (ROA)
  • Handling and report of the OOT, OOS, Incident as per SOP.
  • Receiving specifications, STPs, logbooks, and SOPs from QA.
  • To ensure the daily responsibilities allocated.
  • Any other activity as assigned by the department head/supervisor.

Qualification: B.Pharma, M.Pharma

Experience: 3-4 Years

Salary: 2,00,000 to 4,00,000 INR CTC/PA

Contact Details:


Profiles matching with the above job descriptions only will be considered. If you feel your profile is matching with the above criteria. You can apply for it.

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