Executive, Quality Control, Pharmaceuticals

(0696) Zentiva S.A.

Apply to this job
India / Ankleshwar Until 8/31/2026 2+ years exp First posted July 2, 2026 Last posted July 2, 2026
Job description

JOB TITLE

Executive/Sr. Executive, Quality Control, Pharmaceuticals

Specific additions-

Responsible for LCMS section of Quality control

JOB PURPOSE

Generic

Implement quality control activities for Pharmaceuticals at Ankleshwar adhering to regulatory / global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet with customers’ requirements, living Group’s Values and Code of Ethics.

REQUIREMENTS

Education / Experience

Post Graduate in Science (Organic or Analytical Chemistry )

2-5 years in a Pharmaceutical Company.

Technical skills &

Competencies / Language

  • Analytical ability
  • Trouble shootings
  • Co ordination
  • Communication

KEY ACCOUNTABILITIES

Technical expertise:

Operation and calibration of LCMS/MS instrument for the testing of Nitrosamine, NDSRI as per current regulatory guideline.

Performing Analytical method validation/verification/transfer for Nitrosamine, NDSRI and GTX impurities on LCMS/MS.

Troubleshooting of LCMS instruments during routine use.

Testing

Performing timely analysis of raw material, bulk product, intermediates, finished goods and other samples for Pharmaceuticals.

Performing analysis of market complaints, Stability, process validation samples, Cleaning Validation of Pharmaceuticals.

Testing on nitrosamine and related impurities.

Good Laboratory Practice

Performing calibration & maintenance of lab. Equipment and assisting for the qualification of laboratory equipment.

Reviewing pharmacopeia's for specification preparation.

Preparing SOPs and Formats and Analytical Test Record.

Managing reference standards, working standards, laboratory reagents & chemicals.

Arranging and observing Control Samples and maintaining record.

Participating in Investigation of out of specification results, retesting and review the analysis records.

Maintaining & reviewing laboratory raw data related to testing activity. Validation

Preparing protocol for Analytical Method validation/verification & transfer, cleaning validation and performing the validation exercise as per the protocol for the material and drug products.

Performing analytical method validation/verification & transfer for nitrosamine and NDSRIs using LCMS/MS

Analytical method development and related troubleshooting samples on LCMS/MS.

Management of laboratory Consumables

Identifying and planning requirement for laboratory consumables and monitoring the stock of chemical, spares, glassware and printed material.

Co ordination

Coordinating with production, and warehouse for analytical activities.

Other

Compliance to HSE Requirements for QC Laboratory

Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations.

Carrying out any other assignments or projects as per the instruction of the Dept. Head to meet with the organizational objectives and priorities.     

About this role

Summary

Perform quality control testing, calibration, validation, and troubleshooting of LCMS/MS in pharmaceuticals.

Job title

Executive, Quality Control, Pharmaceuticals

Experience level

2-5 years

Minimum experience

2+ years exp

Industry

pharmaceuticals

Location requirements

India, Ankleshwar; remote work not specified.

Salary

Not specified

Management role

No

Skills & keywords

Required skills

analytical abilitytroubleshootingco ordinationcommunicationlcmsvalidation

Preferred skills

None specified

Specializations

lcmsnitrosaminevalidationanalytical chemistry
Locations

Structured locations inferred from the posting.

Ankleshwar, Gujarat, India

On-site City
Related searches