Hetero Hiring QA – Computer System
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities
- Eligibility / Qualifications
- Relevant Courses
- Required Skills
- Location & Salary
- Application Process
- Why This Opportunity Matters
- Key Highlights
- FAQs
- What is QA CSV in pharma?
- Who can apply for this role?
- Is SAP knowledge mandatory?
- What skills are important for QA CSV jobs?
- How do I apply?
- Summary Table
B.Pharm 1-2 Yrs QA CSV Jobs Jadcherla
B.Pharm, M.Pharm candidates apply for QA CSV role at Hetero Labs Jadcherla. 1–2 yrs experience required. Apply now.
Hetero Labs Limited is actively hiring for Quality Assurance – Computer System Validation (QA CSV) roles at its Jadcherla manufacturing unit. This is a focused opportunity for professionals looking to enter high-value pharmaceutical QA jobs, especially in computer system validation, regulatory compliance, and data integrity. With increasing regulatory scrutiny in pharma manufacturing, QA CSV professionals are in strong demand, making this role highly relevant for long-term career growth in GMP and USFDA-regulated environments.
Company Overview
Hetero Labs Limited is one of India’s leading pharmaceutical companies, widely recognized for its strength in generic drugs, APIs, and global regulatory compliance. The company operates across multiple international markets and maintains high standards aligned with USFDA, EMA, and other global regulatory bodies.
The Jadcherla facility is a key manufacturing site focused on Oral Solid Dosage (OSD) forms. Working in such a facility provides strong exposure to pharmaceutical validation systems, data integrity practices, and digital compliance frameworks, all of which are critical in modern pharma operations.
Job Role & Responsibilities
The QA CSV role focuses on ensuring that computerized systems used in pharmaceutical manufacturing meet regulatory requirements and maintain data integrity.
Core Responsibilities
- Execute computer system validation (CSV) activities in line with GxP guidelines
- Prepare and review validation protocols, reports, and documentation
- Ensure compliance with data integrity and regulatory standards
- Work with SAP systems and ensure proper validation and documentation
- Support audits, inspections, and regulatory submissions
- Maintain lifecycle management of computerized systems
This role is crucial for maintaining compliance in automated pharmaceutical environments, especially where digital systems control production, quality, and data handling.
Eligibility / Qualifications
- Qualification: B.Pharm, M.Pharm
- Experience: 1 to 2 years
- Industry: Pharmaceutical (OSD preferred)
Relevant Courses
B.Pharm, M.Pharm Pharmaceutics, M.Pharm Quality Assurance, M.Pharm Industrial Pharmacy
Required Skills
- Hands-on experience in Computer System Validation (CSV)
- Knowledge of GxP, GMP, and data integrity principles
- Experience in validation documentation and protocols
- Familiarity with SAP systems (preferred)
- Strong understanding of regulatory compliance in pharma
Location & Salary
Location: Jadcherla, Telangana
Salary: As per industry standards (competitive QA pharma salary package based on experience)
This role offers strong career progression in regulatory compliance, validation, and pharmaceutical quality systems.
Application Process
Interested candidates can apply by sending their updated CV to:
Email: ashok.c@hetero.com
Ensure your resume clearly highlights your experience in CSV, validation documentation, and GMP compliance.
Why This Opportunity Matters
Computer System Validation is one of the fastest-growing and highest-value domains in pharmaceutical quality assurance. With increasing reliance on digital systems, regulatory authorities require strict validation and compliance, making CSV professionals highly valuable.
Experience in QA CSV opens career paths in validation engineering, regulatory affairs, and global quality systems. It also significantly increases earning potential in multinational pharmaceutical companies.
Key Highlights
- Company: Hetero Labs Limited
- Department: QA – CSV
- Role: Quality Assurance – Computer System Validation
- Experience: 1–2 Years
- Qualification: B.Pharm, M.Pharm
- Location: Jadcherla
- Industry: Pharmaceutical (OSD Manufacturing)
FAQs
What is QA CSV in pharma?
QA CSV (Computer System Validation) ensures that computerized systems used in pharmaceutical manufacturing meet regulatory and data integrity requirements.
Who can apply for this role?
Candidates with B.Pharm or M.Pharm and 1–2 years of experience in validation or QA can apply.
Is SAP knowledge mandatory?
It is preferred but not mandatory. Having SAP knowledge improves your selection chances.
What skills are important for QA CSV jobs?
Key skills include validation documentation, GxP compliance, data integrity, and system lifecycle management.
How do I apply?
You can apply by sending your updated CV to the provided email ID.
Summary Table
|———————————-|———————————-|
| Company | Hetero Labs Limited |
| Vacancies | QA CSV Executive |
| Required Education | B.Pharm, M.Pharm |
| Experience | 1–2 Years |
|---|
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