AlzaSyno Life Sciences is hiring for the position of Quality Assurance Executive in Clinical Research in Gurugram, Haryana. This opportunity is suitable for professionals with 1–3 years of experience in clinical research, quality assurance, clinical operations, data management, or related areas.
Candidates with a background in Life Sciences, Pharmacy, Clinical Research, Biotechnology, Microbiology, Healthcare, or related fields can apply. Early-career candidates, including freshers with strong knowledge of clinical research quality and compliance, may also be considered based on the provided recruitment information.
AlzaSyno Life Sciences Recruitment 2026 – Overview
| Particulars | Details |
|---|---|
| Company Name | AlzaSyno Life Sciences |
| Job Role | Quality Assurance Executive |
| Department | Clinical Research / Quality Assurance |
| Job Location | Gurugram, Haryana |
| Employment Type | Full-Time |
| Experience | 1–3 Years |
| Freshers | May Be Considered |
| Qualification | Life Sciences, Pharmacy, Clinical Research, Biotechnology, Microbiology, Healthcare or Related Field |
| Work Area | Clinical Research Quality Assurance |
| Application Mode |
Job Summary
The Quality Assurance Executive will support clinical research quality assurance, GCP compliance, audits, quality management systems, CAPA, SOP management, clinical data integrity, and risk-based quality management activities.
The role requires a strong understanding of clinical trial processes and quality standards. The selected candidate will work with cross-functional teams to ensure clinical research activities comply with applicable regulations, company procedures, and quality requirements.
Key Responsibilities
The selected candidate will be responsible for:
- Conducting audits of clinical trial processes.
- Reviewing clinical data management activities.
- Supporting audits of vendors and service providers.
- Ensuring compliance with ICH-GCP and applicable regulatory requirements.
- Ensuring clinical research activities follow company SOPs.
- Supporting the development, review, and implementation of Quality Management Systems (QMS).
- Reviewing and updating SOPs when required.
- Supporting process and system validation activities.
- Reviewing validation activities with a focus on data governance and integrity.
- Assisting with internal audits.
- Supporting sponsor audits and regulatory inspection preparation.
- Tracking CAPA activities and following up on timely closure.
- Reviewing deviations and associated corrective and preventive actions.
- Supporting risk-based quality management activities.
- Monitoring Critical to Quality (CtQ) factors and Key Risk Indicators (KRIs).
- Reviewing clinical study documents, including DMPs, eCRFs, and study reports.
- Supporting GCP and quality compliance training for cross-functional teams.
- Identifying quality and compliance gaps and supporting appropriate corrective actions.
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Educational Qualification
Candidates should have a Bachelor’s or Master’s degree in one of the following fields:
- Life Sciences
- Pharmacy
- Clinical Research
- Biotechnology
- Microbiology
- Healthcare
- Related scientific discipline
Experience Required
The preferred experience range is:
1–3 years
Relevant experience in the following areas can be beneficial:
- Clinical Research QA
- Quality Assurance
- Clinical Operations
- Clinical Data Management
- Regulatory Compliance
- Quality Systems
- Clinical Trial Documentation
Early-career candidates and freshers with a strong understanding of clinical research quality systems may also be considered according to the provided recruitment information.
Required Skills
Technical Skills
Candidates should be familiar with:
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
- Clinical documentation
- Audit tracking
- CAPA follow-up
- EDC systems
Experience with EDC systems will be an added advantage.
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Clinical Research and Quality Skills
Knowledge of the following areas is important:
- ICH-GCP
- Schedule Y
- ICH GCP R3
- Quality Management Systems
- SOPs
- Clinical Trial Processes
- CAPA Management
- Risk-Based Quality Management
- Critical to Quality (CtQ)
- Key Risk Indicators (KRIs)
- Data Governance
- Clinical Data Integrity
- Clinical Trial Audits
- Regulatory Compliance
Who Can Apply?
This opportunity can be suitable for candidates who have an academic background in Pharmacy, Life Sciences, Biotechnology, Microbiology, Clinical Research, or Healthcare.
Professionals with 1–3 years of relevant experience will be suitable for the role. Candidates at an early stage of their career may also be considered if they demonstrate strong knowledge of GCP, clinical trial documentation, quality systems, and compliance requirements.
Salary Details
The estimated salary range for the Quality Assurance Executive position is:
₹3 LPA – ₹5.5 LPA
This is an estimated range and not an officially disclosed salary package. Actual compensation may vary depending on qualification, experience, clinical research exposure, QA skills, interview performance, and company policies.
Benefits
Specific employee benefits have not been clearly mentioned in the provided recruitment information.
Job Location
Gurugram, Haryana, India
Employment Type: Full-Time
Career Opportunity
This position can be a useful opportunity for professionals looking to develop a career in Clinical Research Quality Assurance and Regulatory Compliance.
The role provides exposure to areas such as:
- Clinical Trial Auditing
- GCP Compliance
- Quality Management Systems
- CAPA
- SOP Management
- Clinical Data Integrity
- RBQM
- Regulatory Inspection Readiness
- Clinical Documentation
- Vendor Quality Management
Experience in these areas can support future career opportunities in Clinical QA, Quality Compliance, Clinical Operations, Regulatory Affairs, and Clinical Data Management.
How to Apply
Interested and eligible candidates can send their updated CV to:
Email: hr@alzasyno.com
Candidates should mention “Quality Assurance Executive” in the email subject line.
Applicants should ensure their resume highlights relevant knowledge or experience in GCP, clinical research, audits, QMS, SOPs, CAPA, RBQM, clinical data integrity, and regulatory compliance.
Frequently Asked Questions (FAQs)
What is the job role at AlzaSyno Life Sciences?
The company is hiring for Quality Assurance Executive in Clinical Research.
Where is the job located?
The position is based in Gurugram, Haryana.
How much experience is required?
The preferred experience is 1–3 years in clinical research QA, compliance, clinical operations, data management, or related areas.
Can freshers apply?
Freshers or early-career candidates with strong knowledge of clinical research quality and compliance may be considered, based on the provided recruitment information.
What qualification is required?
Candidates with a degree in Life Sciences, Pharmacy, Clinical Research, Biotechnology, Microbiology, Healthcare, or a related field can apply.
What is the estimated salary?
The estimated salary is ₹3 LPA to ₹5.5 LPA. The actual salary may vary.
How can candidates apply?
Candidates can email their updated CV to hr@alzasyno.com with “Quality Assurance Executive” as the email subject.
