QA Manager Job in Hyderabad & Gurugram at Syneos Health. Apply now for GxP audit leadership role before deadline.
Introduction
If you are an experienced quality assurance professional in the clinical research or pharmaceutical domain, this is a high-impact leadership opportunity. A globally recognized CRO is hiring QA Managers for hybrid roles in India. This position offers exposure to regulatory audits, global quality systems, and team leadership within a fast-paced drug development environment.
Company Overview
Syneos Health is a leading integrated biopharmaceutical services organization that supports pharmaceutical and biotech companies across the entire drug development lifecycle. From early-phase research to commercialization, the company plays a critical role in accelerating healthcare innovation. With a strong global presence and thousands of professionals worldwide, it offers a collaborative and growth-oriented work environment.
Job Overview
| Job Details | Information |
|---|---|
| Job Role | Manager, Quality Assurance (QA) |
| Company | Syneos Health |
| Location | Hyderabad / Gurugram |
| Experience | Experienced Professionals |
| Qualification | Bachelor’s in Science / Healthcare |
| Employment Type | Full-Time (Hybrid) |
| Job ID | 25103098 |
| Last Date | March 27, 2026 |
Job Location & Employment Type
- Locations: Hyderabad and Gurugram (Hybrid model)
- Employment Type: Full-time
- Work Mode: Combination of office and remote work
Open Positions / Department Details
- Department: Quality Assurance (QA)
- Role Level: Managerial
- Reporting: Leadership role with team supervision responsibilities
- Travel: Up to 25% (as per project needs)
Key Roles & Responsibilities
As a QA Manager, you will oversee quality systems, audits, and regulatory compliance across clinical and operational processes. Your responsibilities will include:
- Planning and conducting GxP audits in line with internal SOPs and regulatory standards
- Reviewing and approving audit reports while ensuring accuracy and compliance
- Preparing and managing customer and regulatory authority inspections
- Conducting mock inspections and developing inspection readiness strategies
- Coordinating audit responses and resolving compliance issues with stakeholders
- Leading root cause analysis and implementing CAPA (Corrective and Preventive Actions)
- Providing expert guidance on quality-related matters across teams
- Managing and mentoring QA staff, including performance and development
- Supporting corporate quality projects and ensuring timely execution
- Enhancing QA SOPs and work instructions for continuous improvement
Eligibility Criteria
Education
- Bachelor’s degree in Science, Life Sciences, or Healthcare-related field
- Equivalent experience may also be considered
Experience
- Significant experience in GxP Quality Assurance auditing
- Hands-on experience in multiple audit types such as:
- Investigator site audits
- Vendor audits
- Trial Master File (TMF) audits
- Data management and safety reporting audits
- Laboratory audits
Skills Required
Candidates should demonstrate:
- Strong knowledge of GxP regulations and compliance standards
- Expertise in audit processes and inspection readiness
- Excellent analytical and problem-solving abilities
- Leadership and team management skills
- Strong organizational and multitasking capability
- Effective communication and report-writing skills
- Ability to handle complex compliance issues independently
- Proficiency in MS Office and basic SharePoint tools
- Strong interpersonal and stakeholder management skills
Salary & Benefits
- Salary: As per company norms
- Career development and internal growth opportunities
- Training in technical and therapeutic areas
- Recognition and rewards programs
- Inclusive and collaborative work culture
- Exposure to global clinical research projects
Selection Process
The hiring process typically includes:
- Resume screening
- Technical and functional interview rounds
- Leadership/managerial discussion
- HR interview and final offer
How to Apply
Interested candidates should apply through the official careers portal of the company.
- Job ID: 25103098
- Apply before the deadline to avoid missing this opportunity
Important Dates
- Last Date to Apply: March 27, 2026 (Limited time remaining)
Why Apply for This Pharma Job?
This role is ideal for experienced QA professionals aiming to move into leadership positions within the CRO industry. By applying, you will:
- Lead global quality assurance and audit operations
- Work on regulatory inspections and compliance strategies
- Gain exposure to international clinical research standards
- Develop leadership and team management expertise
- Be part of a globally recognized healthcare organization
This position offers both professional growth and the opportunity to contribute to improving healthcare quality worldwide.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform. We are not associated with Syneos Health or its hiring team. We only provide job-related information for awareness purposes. Candidates should verify all details independently before applying.
Final Call-to-Action
If you have strong experience in quality assurance and regulatory audits, this is a premium opportunity to advance your career. Apply immediately before the deadline and take the next step in your QA leadership journey.
