AlzaSyno Life Sciences is hiring for the role of Quality Assurance Executive in Gurugram, Haryana. This opportunity is suitable for early-career professionals who want to build a career in clinical research quality assurance, regulatory compliance, and clinical data integrity.
The role focuses on clinical trial audits, GCP compliance, quality management systems, SOPs, CAPA tracking, and risk-based quality management. Candidates with a strong understanding of clinical research, documentation, and quality standards can consider applying.
Quick Answer: AlzaSyno Life Sciences is hiring a Quality Assurance Executive in Gurugram. Candidates with life sciences, pharmacy, clinical research, or related backgrounds and skills in GCP, QMS, CAPA, audits, SOPs, and clinical trial compliance can apply.
Job Overview
| Details | Information |
|---|---|
| Company | AlzaSyno Life Sciences |
| Role | Quality Assurance Executive |
| Location | Gurugram, Haryana |
| Job Type | Full-time |
| Experience | 1–3 years |
| Qualification | Life Sciences, Pharmacy, Clinical Research, Healthcare, Biotechnology, Microbiology, or related field |
| Salary Estimate | ₹3 LPA – ₹5.5 LPA |
| Posted Date | Not specified |
| Last Date | Not specified |
Responsibilities
Selected candidates will be responsible for:
- Conducting audits of clinical trial processes, data management activities, and vendor operations.
- Ensuring compliance with ICH-GCP, applicable regulatory requirements, and company SOPs.
- Supporting the development, review, and implementation of QMS and SOPs.
- Reviewing process and system validation activities with a focus on data governance.
- Assisting in internal audits, sponsor audits, and regulatory inspection preparation.
- Managing CAPA activities, including tracking, review, and timely closure of deviations.
- Supporting risk-based quality management activities, including CtQ data and KRIs.
- Reviewing clinical study documents such as DMPs, eCRFs, and study reports.
- Providing GCP and quality compliance training support to cross-functional teams.
Qualifications / Who Can Apply
Candidates with the following backgrounds may be suitable:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, Microbiology, Clinical Research, Healthcare, or a related field.
- Candidates with 1–3 years of experience in clinical research QA, compliance, clinical operations, data management, or related areas.
- Early-career professionals with strong knowledge of GCP, clinical trial documentation, and quality systems may also be considered if they match the role requirements.
Skills Required
Technical skills:
- MS Word, Excel, and PowerPoint
- EDC system familiarity is an added advantage
- Documentation review
- Audit tracking and CAPA follow-up
Domain skills:
- ICH-GCP knowledge
- Schedule Y awareness
- ICH GCP R3 familiarity
- QMS and SOP understanding
- Clinical trial process knowledge
- CAPA management
- RBQM, CtQ, and KRI awareness
- Data governance and clinical data integrity
Soft skills:
- Attention to detail
- Analytical thinking
- Problem-solving ability
- Written and verbal communication
- Team collaboration
- Compliance-focused mindset
Salary
Estimated salary range: ₹3 LPA – ₹5.5 LPA
The actual salary may vary depending on the candidate’s experience, interview performance, clinical research exposure, and QA/compliance skills.
Benefits
Benefits were not clearly specified in the job description.
How to Apply
Interested candidates can send their updated CV to:
Candidates should mention the role name “Quality Assurance Executive” in the email subject line while applying.