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PHARMA JOBS POST > Pharma Jobs > Exciting Career Opportunity in Quality Assurance at Gland Pharma Limited
Pharma Jobs

Exciting Career Opportunity in Quality Assurance at Gland Pharma Limited

Sunil Kumar Swain
Last updated: October 14, 2025 1:23 pm
Sunil Kumar Swain 8 months ago
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Walk-In Interview for Experienced Sterile Injectables Professionals

Gland Pharma Limited is hosting an exciting career opportunity for quality assurance professionals with expertise in sterile injectables. If you’re an experienced professional looking to take the next step in your career, this could be the perfect opportunity for you.

Contents
Position DetailsEligibility RequirementsKey Responsibilities and Required SkillsHow to Apply?Important Disclaimer

Position Details

Department: Quality Assurance

Job Location: MPSF Plant (Unit-II), Gland Pharma Limited, Unit – 2 Plot No: 42-52, Phase III, TSIC, Pashamylaram

Interview Date: Friday, October 17th, 2025

Time: 9:30 AM – 11:30 AM

Eligibility Requirements

The company is seeking candidates with the following qualifications and experience:

Educational Background: B. Pharm, M. Pharm, B.Sc, or M.Sc

Experience: 5 to 8 years of relevant experience in sterile injectables manufacturing and quality assurance

Key Responsibilities and Required Skills

As a Quality Assurance professional at Gland Pharma, you will be responsible for a range of critical tasks related to batch production and control. Your expertise should encompass:

– Comprehensive review of master Batch Production and Control Records (BPCR) and media fill procedures

– Management of batch protocols, reports, and submission documentation

– Issuance of BPCR documentation as per batch requisitions and handling of batch cancellations or planning changes

– Thorough review of completed BPCR for data accuracy and compilation prior to final release

– Reporting deviations in BPCR documentation to Head QA and Storage departments with appropriate retrieval of executed records

– Review of media fill records and preparations of media fill reports

– Development and review of Standard Operating Procedures (SOPs) and batch submission protocols

– Preparation and assessment of Process Validation protocols and reports

– Preparation and review of Cleaning Validation protocols, reports, and Bill of Materials (BOMs)

– Dispatch coordination of finished products according to customer specifications

– In-depth knowledge of Batch Release and Process Validation procedures

How to Apply?

Candidates interested in this opportunity are encouraged to share their profiles directly with the recruitment team at suryateja.velaga@glandpharma.com

Note for Outstation Candidates: Candidates from outstation locations are particularly welcome to apply and are encouraged to share their profiles via email.

Important Disclaimer

Gland Pharma Limited does not seek any form of payment from prospective candidates for employment opportunities or authorize any agency or individual to collect fees for recruitment purposes. Please be cautious of fraudulent schemes and apply directly through official channels.

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