Zentiva
Executive Quality Control, Pharmaceuticals
India · Work style not stated · Full time
Apply on the employer’s site ↗See how well you match this job
You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.
About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerZentiva
- LocationIndia
- Work styleWork style not stated
- Employment typeFull time
- Employer posted
JOB TITLE
Executive Quality Control, Pharmaceuticals
REQUIREMENTS
Education / Experience
Post Graduate in Science (Organic or Analytical Chemistry )
1-4years 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.
Show full description
Performing analysis of market complaints, Stability, process validation samples,Cleaning Validation of Pharmaceuticals.
Good Laboratory Practice
Performing calibration & maintenanceof 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.
Check your resume against this job Free, no sign-up. Nothing you paste is stored.
Staying safe while you apply
- Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
- Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
- Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.
Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.
Preparing for this role with ROLIVA
- Check the fit.
Compare the requirements with the experience you have confirmed, including gaps.
- Prepare honestly.
Build interview stories and application drafts from your own evidence.
- Keep track.
Save the role and record your own application status and follow-ups.
At a glance
- Employment typeFull time
- Employer posted
- Added to ROLIVA
- Last checked