India's DMPLOI - Jobs & Networking AppS Kant Healthcare Ltd., a leading pharmaceutical company based in Vapi, Gujarat, has announced an exciting career opportunity for experienced Quality Assurance professionals. The company is looking to hire an APQR Executive (QA) to strengthen its Quality Assurance team and support continuous improvement initiatives in product quality and regulatory compliance.
This opportunity is ideal for candidates with experience in Annual Product Quality Review (APQR), GMP compliance, quality systems, documentation practices, deviation management, CAPA, and cross-functional coordination within the pharmaceutical industry.
Job Details
Particulars Details
Company Name
S Kant Healthcare Ltd.
Position
APQR Executive (QA)
Department
Quality Assurance (QA)
Location
Vapi, Gujarat
Qualification
B.Pharm / M.Pharm
Experience
3–5 Years
Industry
Pharmaceutical Manufacturing
Key Responsibilities
The selected candidate will be responsible for:
Preparation and review of Annual Product Quality Review (APQR) reports.
Analysis of product quality trends and process performance data.
Coordination with Production, QC, QA, and Regulatory Affairs departments.
Review of deviations, change controls, complaints, and CAPA records for APQR.
Ensuring compliance with GMP guidelines and regulatory requirements.
Monitoring quality metrics and identifying opportunities for continuous improvement.
Supporting regulatory inspections and internal audits.
Required Skills & Qualifications
Candidates applying for this role should possess:
B.Pharm or M.Pharm qualification.
3–5 years of pharmaceutical Quality Assurance experience.
Strong knowledge of APQR preparation and review.
Good understanding of GMP, documentation practices, and regulatory requirements.
Experience in handling deviations, CAPA, change control, and complaint investigations.
Excellent analytical and communication skills.
Why Join S Kant Healthcare Ltd.?
S Kant Healthcare Ltd. is recognized for its commitment to quality, innovation, integrity, and excellence in pharmaceutical manufacturing. Employees gain exposure to advanced quality systems, regulatory compliance practices, and opportunities for professional growth within a dynamic work environment.
The company focuses on:
Quality-driven operations
Regulatory compliance excellence
Employee development
Continuous process improvement
Innovation in pharmaceutical manufacturing
How to Apply
Interested and eligible candidates can share their updated CV at:
latesh.nemade@skant.com
Location: S Kant Healthcare Ltd., Vapi, Gujarat
Technical FAQs – APQR Executive (QA)
1. What is APQR in the pharmaceutical industry?
APQR (Annual Product Quality Review) is a periodic evaluation of all quality-related data of a product to verify process consistency, identify trends, and ensure continued compliance with GMP and regulatory requirements.
2. What data is typically reviewed during APQR preparation?
APQR includes review of:
Batch manufacturing records
Analytical results
Deviations
OOS/OOT investigations
Change controls
Complaints
Stability data
CAPA effectiveness
Yield and process performance trends
3. Why are deviations and CAPA important in APQR?
Deviation and CAPA reviews help identify recurring quality issues, evaluate corrective actions, and ensure continuous improvement in manufacturing processes and product quality.
4. How does APQR support regulatory compliance?
APQR demonstrates ongoing monitoring of product quality and manufacturing performance, helping companies comply with GMP requirements issued by regulatory authorities such as USFDA, MHRA, EMA, and WHO-GMP.
5. What GMP knowledge is essential for an APQR Executive?
An APQR Executive should understand:
Good Documentation Practices (GDP)
Data Integrity principles
Deviation management
Change control systems
CAPA management
Risk assessment tools
Regulatory guidelines related to product quality review
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