Pharma Jobs at Parexel – Apply For Specialist Role
Looking to build a rewarding career in technology compliance within the pharmaceutical industry? Parexel, a global leader in drug development and consulting, is hiring a System Validation Services – Specialist II in multiple Indian locations. This role offers a unique opportunity to work at the forefront of quality management and system validation in a dynamic, fast-paced environment.
About Parexel
Parexel is a leading global consulting company specializing in the pharmaceutical and biotechnology industries. We offer a range of services to help our clients accelerate the development of new therapies and efficiently bring them to market.
Job Title: System Validation Services – Specialist II
Job ID: R0000032694
Category: Quality Management
Location: Various locations in India – Bengaluru, Chandigarh, Hyderabad, Mohali, and Mumbai
Description:
The Parexel System Validation Services (SVS) team supports and enhances the compliance of the company’s technology solutions and offerings through standardized validation activities based on current GxP requirements and risk management principles. We are looking for a Specialist II to join our team.
Key Responsibilities:
- Lead specific tasks for executing the Parexel system’s validation strategy
- Plan and oversee a risk-based approach to system validation
- Provide validation consultancy and oversight to ensure compliance with regulatory requirements
- Conduct periodic reviews to verify the validated state of technology solutions
- Support risk management activities to identify and control technology-related risks
Skills and Qualifications:
- Entry/mid-level experience in computer technology, quality, and compliance
- Basic knowledge of continuous improvement methodologies
- Strong interpersonal, communication, and organizational skills
- Ability to work in a fast-paced environment and manage multiple tasks
- Highly motivated and client-focused
Education:
Educated to degree level in technology, biological science, pharmacy, or equivalent qualification or 3+ years clinical research experience.
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