Job Title: Quality Assurance Associate
Location: Hyderabad, India (Hybrid Work Model)
Job ID: 25105204
Employment Type: Full-Time
Industry: Clinical Research | Pharmaceutical Quality Assurance | CRO | Regulatory Compliance
Syneos Health is inviting applications for the position of Quality Assurance Associate at its Hyderabad office under a hybrid work model. This role is designed for professionals seeking to build expertise in clinical quality assurance, audit support, and regulatory compliance within a global Contract Research Organization (CRO).
As a leading biopharmaceutical solutions organization operating in more than 110 countries, Syneos Health supports clinical development, medical affairs, and commercialization services for pharmaceutical and biotechnology companies worldwide.
The Quality Assurance Associate supports audit scheduling, regulatory inspection preparation, and enterprise quality management system (eQMS) documentation. The position plays a vital role in ensuring compliance with GCP, GxP, and global regulatory standards while contributing to inspection readiness initiatives.
This opportunity is suitable for candidates interested in developing a career in:
Clinical Quality Assurance (CQA)
Pharmaceutical Compliance
Regulatory Affairs Support
Audit Coordination
Enterprise Quality Management Systems (eQMS)
Assist in tracking planned and scheduled audits within the enterprise quality management system.
Update audit schedules and compliance calendars as directed by management.
Compile documentation required for internal audits, customer audits, and regulatory inspections, including:
Training records
Organizational charts
Standard Operating Procedures (SOPs)
Quality and compliance documentation
Support auditors in gathering follow-up information during inspections.
Accurately enter audit-related data into the eQMS.
Maintain, file, and archive Quality Assurance documentation in compliance with regulatory requirements.
Ensure document control, version tracking, and data accuracy.
Assist in preparing QA tools, trackers, and compliance documentation templates.
Contribute to inspection readiness and continuous quality improvement initiatives.
Perform other QA-related responsibilities as assigned.
Work under structured supervision with detailed instructions for daily tasks.
Minimal travel may be required (up to 25%).
0–2 years of experience in healthcare, pharmaceutical, biotechnology, or clinical research environments.
Exposure to quality systems, regulatory documentation, compliance processes, or audit coordination is preferred.
Fresh graduates with relevant internships in clinical operations, QA, or regulatory functions may also be considered.
Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Healthcare Management, or a related field.
Equivalent education combined with relevant professional experience may be considered.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
Basic knowledge of SharePoint or electronic document management systems is advantageous.
Strong organizational and time management skills.
Ability to handle multiple priorities and meet deadlines in a dynamic environment.
Strong written and verbal communication skills.
Attention to detail and documentation accuracy.
Ability to work effectively with culturally diverse global stakeholders.
Hybrid work model based in Hyderabad, India.
Exposure to global pharmaceutical and clinical research quality frameworks.
Opportunity to gain hands-on experience in GCP and GxP compliance.
Structured corporate environment with clear career progression pathways.
Potential career advancement opportunities include:
Clinical Quality Assurance Specialist
QA Auditor
Regulatory Affairs Associate
Quality Systems Analyst
Syneos Health is a globally recognized biopharmaceutical solutions company that has supported 94% of novel FDA-approved drugs and 95% of EMA-authorized products in recent years. With more than 29,000 professionals worldwide, the organization collaborates across thousands of clinical trial sites to advance medical innovation.
If you are seeking to build a career in Pharmaceutical Quality Assurance, Clinical Compliance, or Audit Support, this hybrid opportunity in Hyderabad offers valuable exposure to global regulatory standards within a leading CRO environment.
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