Aizant Hiring 2026 | Bioanalytical Department | Multiple Open Positions

Published onJuly 31, 2026

Bioanalytical, Analyst |Operator | Group Leader

Aizant

B.Sc., M.Sc., B.Pharmacy, M.Pharmacy
Kompally, Hyderabad
1–6 Years
Job Posted Date:31/07/2026

Job Overview

Aizant is hiring experienced professionals for its Bioanalytical Department at its Kompally, Hyderabad facility. The company is inviting applications for Analyst, Operator, and Group Leader positions. Candidates with experience in LC-MS/MS, method development, validation, sample analysis, and laboratory documentation are encouraged to apply.

Immediate joiners are preferred.

Company Name

Aizant

Department

Bioanalytical

Job Location

Kompally, Hyderabad

Open Positions

Analyst

  • Experience: 1–3 Years

Operator

  • Experience: 3–6 Years

Group Leader

  • Experience: Above 6 Years

Educational Qualification

Candidates with the following qualifications are eligible:

  • B.Sc.

  • M.Sc.

  • B.Pharmacy

  • M.Pharmacy

Job Responsibilities

Analyst

  • Perform method development, method validation, and routine sample analysis using LC-MS/MS.

  • Handle supporting laboratory instruments.

  • Maintain documentation as per Good Documentation Practices (GDP).

  • Perform calibration, maintenance, and sample analysis.

  • Participate in study report preparation and system development.

  • Coordinate with instrumentation engineers and support SOP-related activities.

  • Perform other assigned laboratory responsibilities.

Operator

  • Conduct method development, validation, and routine sample analysis using LC-MS/MS.

  • Operate and maintain analytical instruments (LC-MS/MS).

  • Prepare and maintain documentation according to Good Documentation Practices.

  • Perform instrument calibration, maintenance, and sample analysis.

  • Train junior analysts and support system development activities.

  • Coordinate with instrumentation engineers and assist in SOP implementation.

  • Carry out additional responsibilities as assigned.

Group Leader

  • Lead method development, validation, and sample analysis using LC-MS/MS.

  • Address Quality Assurance (QA), sponsor, and regulatory queries.

  • Prepare study reports and coordinate with cross-functional teams including QC, Report Writers, and eCTD teams.

  • Mentor team members, review SOPs, provide training, and support laboratory development.

  • Ensure compliance with GCP, GLP, and regulatory requirements.

  • Perform other assigned responsibilities as required.

How to Apply

Interested candidates can forward their updated resume to:

Email: sonyjeevitha.degala@aizant.com

Additional Information

  • Immediate joiners are welcome.

  • Candidates should have relevant experience in bioanalytical laboratory operations and LC-MS/MS techniques.

  • Strong documentation practices and regulatory compliance knowledge will be an added advantage.

How to Apply

Poster 1