hirly

Zentiva

Executive Quality Control, Pharmaceuticals

India / Ankleshwar

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at Zentiva first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included

Matched against 2.3M live jobs from 200,000+ employers in 200+ countries.

Tailor my resume for this job →

hirly's read of this role

Seniority
Mid level
Country
IN
Work mode
On-site / unstated
First seen by hirly
17 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

JOB TITLE

Executive Quality Control, Pharmaceuticals

REQUIREMENTS

Education / Experience

Post Graduate in Science (Organic or Analytical Chemistry )

1-4 years in a Pharmaceutical Company .

Technical skills &

Competencies / Language

Analytical ability

Trouble shootings

Co ordination

Communication

Behavioural Competencies

(LEAD and others)

Accountability , Authenticity, Collaboration, Courage and Trust

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.

KEY ACCOUNTABILITIES

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.

Good Laboratory Practice

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

Reviewing pharmacopeias 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, cleaning validation and performing the validation exercise as per the protocol.

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.

Original posting on Zentiva's site ↗

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job