India's DMPLOI - Jobs & Networking AppKwality Pharmaceuticals Ltd., a leading pharmaceutical manufacturing company with EU-GMP certified facilities, has announced exciting career opportunities for experienced Quality Control professionals. The company is currently seeking qualified candidates for the position of QC Reviewer & STP Preparations (QMS) to strengthen its quality systems and regulatory compliance functions.
This opportunity is ideal for professionals with strong expertise in Quality Management Systems (QMS), Standard Test Procedure (STP) preparation, documentation review, and cGMP compliance.
Position Details
Particulars Details
Position
QC Reviewer & STP Preparations
Department
Quality Control (QMS)
Experience
5–6 Years
Industry
Pharmaceutical Manufacturing
Location
Amritsar, Punjab
Company
Kwality Pharmaceuticals Ltd.
Key Responsibilities
The selected candidate will be responsible for ensuring quality compliance and maintaining robust documentation systems across QC operations.
Major responsibilities include:
Reviewing and evaluating quality control data, reports, and analytical documentation.
Ensuring compliance with quality standards, specifications, and regulatory requirements.
Identifying quality-related issues and recommending corrective actions.
Preparing, reviewing, and verifying Standard Test Procedures (STPs).
Maintaining accuracy, completeness, and consistency of QC documentation.
Collaborating with cross-functional departments for effective implementation of quality systems.
Supporting Quality Management System (QMS) activities and compliance initiatives.
Required Skills & Qualifications
Candidates applying for this role should possess:
Strong understanding of Quality Control and Quality Management Systems (QMS).
Hands-on experience in STP preparation, review, and approval processes.
Knowledge of cGMP, EU-GMP, and regulatory documentation requirements.
Proficiency in MS Office and documentation management tools.
Excellent analytical, communication, and problem-solving abilities.
Strong attention to detail and documentation accuracy.
Why Join Kwality Pharmaceuticals?
Kwality Pharmaceuticals operates EU-GMP certified manufacturing facilities and has built a reputation for maintaining high-quality pharmaceutical standards. Working with the organization offers:
Exposure to global regulatory requirements.
Opportunities to work in a highly compliant quality environment.
Professional growth in quality systems and documentation management.
Collaborative work culture with experienced pharmaceutical professionals.
Career advancement opportunities in regulatory and quality functions.
Application Process
Interested candidates can forward their updated CV through the following channels:
Email: career@kwalitypharma.com
WhatsApp: +91 9056855224
Company Address:
Kwality Pharmaceuticals Ltd.
Village Nag Kalan, Majitha Road, Amritsar – 143601, Punjab, India
Technical FAQs
1. What is the purpose of an STP (Standard Test Procedure) in Quality Control?
An STP provides detailed instructions for performing analytical tests consistently and accurately. It ensures uniformity, compliance with regulatory requirements, and reliable test results across laboratories.
2. How does a QC Reviewer contribute to GMP compliance?
A QC Reviewer verifies analytical data, calculations, test reports, and documentation to ensure accuracy, integrity, and compliance with cGMP and regulatory standards before final approval.
3. What are the key elements of an effective Quality Management System (QMS)?
An effective QMS includes document control, change management, deviation handling, CAPA (Corrective and Preventive Actions), training management, risk assessment, and continuous improvement processes.
4. Why is data integrity important in pharmaceutical Quality Control?
Data integrity ensures that all records are accurate, complete, consistent, and attributable throughout their lifecycle. Regulatory agencies such as USFDA and EMA consider data integrity critical for product quality and patient safety.
5. What is the difference between cGMP and EU-GMP requirements?
Both focus on pharmaceutical quality and patient safety. EU-GMP places additional emphasis on quality risk management, validation practices, and documentation controls, while cGMP provides broader global manufacturing guidelines. Companies operating in international markets often comply with both standards.
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