Syneos Hiring QA Clinical Operations Associate

Syneos Health Quality Assurance Associate Recruitment

Syneos Health is currently hiring for the Quality Assurance Associate role at its Serilingampalli location in Telangana, India. This opening is part of the Quality Assurance and Clinical Operations support function and is well suited for early-career professionals seeking entry-level or junior roles in clinical research quality systems. The position is offered on a full-time, hybrid work model and is ideal for candidates with minimal experience who want to build a long-term career in biopharmaceutical quality assurance and audit compliance within a global organization.

Company Overview

Syneos Health is a globally recognized, fully integrated biopharmaceutical solutions organization supporting pharmaceutical, biotechnology, and healthcare companies across the entire product lifecycle. With operations spanning more than 110 countries and a workforce of over 29,000 professionals, the organization plays a critical role in advancing clinical development, medical affairs, and commercial execution.

The company is widely known for its contribution to regulatory success, having supported the majority of recent novel FDA-approved drugs and EMA-authorized products. Syneos Health operates with a strong quality culture, robust governance frameworks, and enterprise-level quality management systems that ensure compliance with global regulatory standards. Its focus on people development, ethical practices, and continuous improvement makes it a trusted partner in global healthcare advancement and a preferred employer for clinical research professionals.

Job Role & Responsibilities

The Quality Assurance Associate role supports the enterprise quality and auditing function by ensuring accurate documentation, audit readiness, and effective coordination with internal and external stakeholders. This position plays a foundational role in maintaining compliance and supporting regulatory inspections across clinical and healthcare operations.

Key Responsibilities

  • Supporting the tracking of planned and scheduled audits within the enterprise quality management system
  • Updating audit schedules, calendars, and related documentation as directed by management
  • Assisting in the collection and preparation of documentation required for audits and inspections, including training records and organizational charts
  • Coordinating with auditors to provide follow-up documentation during customer audits and regulatory inspections
  • Entering and maintaining audit-related data within the quality management system
  • Filing, archiving, and maintaining Quality Assurance documentation in compliance with internal procedures
  • Supporting the auditing team to ensure inspection readiness across functions
  • Performing additional quality-related tasks as assigned by management
  • Supporting cross-functional teams while maintaining confidentiality and data integrity

Minimal travel may be required for this role, depending on audit and inspection needs.

Eligibility / Qualifications

Educational Qualification

  • Bachelor’s degree or equivalent in a relevant discipline

Experience Requirement

  • Minimal experience in a healthcare, clinical research, or regulated environment is acceptable
  • Entry-level and early-career candidates are encouraged to apply

Skill Requirements

  • Working knowledge of computer applications including Microsoft Office and basic SharePoint
  • Ability to manage multiple tasks and meet timelines in a dynamic work environment
  • Strong organizational and documentation skills
  • Effective written and verbal communication abilities
  • Interpersonal skills to collaborate with diverse, cross-cultural teams
  • Attention to detail and a structured approach to quality documentation

Eligible Courses (Comma-Separated)

BSc Life Sciences, BSc Biotechnology, BSc Clinical Research, BPharm, MPharm, BSc Nursing, Bachelor’s in Health Sciences

Location & Salary

Job Location

Serilingampalli, Telangana, India

Work Model

Hybrid | Full-time

Salary Information

Compensation will be offered as per company standards and aligned with the candidate’s education, experience, and internal role leveling. The position offers strong exposure to enterprise quality systems, audit coordination, and regulated clinical research environments, supporting long-term career progression in quality assurance and compliance roles.

Syneos Health Quality Assurance Associate Recruitment
Syneos Health Quality Assurance Associate Recruitment

Application Process

Interested candidates should apply through the official Syneos Health careers portal. Applications are reviewed centrally and responses are managed outside of LinkedIn.

How to Apply

Apply online using the link below:

https://syneoshealth.wd12.myworkdayjobs.com/Syneos_Health_External_Site/job/IND-Hyderabad-Hybrid/Quality-Assurance-Associate_25105204/apply?bid=0&tid=x_340a0149-57dd-4ac8-9021-3df97056d0ca

Applicants are advised to keep documentation-related experience and compliance exposure clearly highlighted in their resumes.

FAQs

Who can apply for the Quality Assurance Associate role?

Candidates with a bachelor’s degree and minimal experience in healthcare or clinical research environments can apply.

Is this role suitable for freshers?

Yes. This role is suitable for entry-level and early-career professionals looking to start a career in quality assurance.

What type of work model is offered?

The position follows a hybrid work model with on-site and remote components.

Does the role involve travel?

Minimal travel may be required, up to approximately 25%, depending on audit requirements.

How do I apply for this position?

Applications must be submitted through the official Syneos Health Workday application link.

Summary Table

Company Syneos Health
Vacancies Quality Assurance Associate
Required Education BSc Life Sciences, BSc Biotechnology, BPharm, MPharm, BSc Clinical Research
Experience Entry-Level / Minimal Experience

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To apply for this job please visit syneoshealth.wd12.myworkdayjobs.com.

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