Responsible for validating computerized systems in a GxP-regulated pharmaceutical environment. The role involves authoring and reviewing validation documentation, executing compliance procedures, applying GDP, GAMP5, FDA, and 21 CFR Part 11 standards, managing the end-to-end validation lifecycle, and mentoring teams on regulatory and client requirements.
Project Role : Business Architect
Project Role Description : Identify opportunities to deliver tangible business value by assessing the current state, capturing high-level requirements, and defining business solutions. Translate business needs into technology-enabled solutions and operating models. Support transformation by developing business cases and guiding implementation of key initiatives.
Must have skills : Computer System Validation (CSV)
Good to have skills : NA
Minimum 3 year(s) of experience is required
Educational Qualification : 15 years full time education
Summary:
A skilled Computerized System Validation (CSV) professional responsible for ensuring compliance and validating computerized systems within a GxP-regulated pharmaceutical environment. This role involves authoring crucial validation documentation, mentoring teams on regulatory standards (including FDA, GAMP5, and 21 CFR Part 11), and maintaining strict adherence to Good Documentation Practices (GDP) throughout the validation lifecycle.
Roles & Responsibilities:
- Documentation Management: Draft, evaluate, and peer-review essential validation documentation in strict accordance with Good Documentation Practices (GDP).
- System Validation: Execute and oversee compliance and validation procedures specifically tailored for computerized systems.
- Team Mentorship: Coach and guide team members to ensure they fully grasp and consistently apply client workflows and project validation goals.
Professional & Technical Skills:
- Regulatory Knowledge: Expertise in Pharmaceutical Regulatory Compliance and Computerized System Validation (CSV).
- Industry Frameworks: Strong practical background in GxP environments, encompassing the complete validation lifecycle and the V-Model framework.
- Documentation Standards: Deep understanding and application of Good Documentation Practices (GDP).
- Compliance Guidelines: Thorough familiarity with GAMP5 industry standards and FDA regulatory guidelines.
- Project Lifecycle: Proven experience managing the end-to-end validation lifecycle for highly regulated projects.
- Communication & Analysis: Excellent analytical capabilities paired with strong interpersonal communication skills.
- Critical Thinking: Highly effective problem-solving and troubleshooting abilities.
Additional Information:
- Degree: Bachelor of Engineering (BE) degree or an equivalent academic credential.
- Core Competencies: CSV, General System Validation, FDA 21 CFR Part 11 compliance, and Computerized System Validation methodologies.
- The candidate should have minimum 5 years of experience
- This position is based at our Chennai office.
- A 15 years full time education is required.15 years full time education
Project Role Description : Identify opportunities to deliver tangible business value by assessing the current state, capturing high-level requirements, and defining business solutions. Translate business needs into technology-enabled solutions and operating models. Support transformation by developing business cases and guiding implementation of key initiatives.
Must have skills : Computer System Validation (CSV)
Good to have skills : NA
Minimum 3 year(s) of experience is required
Educational Qualification : 15 years full time education
Summary:
A skilled Computerized System Validation (CSV) professional responsible for ensuring compliance and validating computerized systems within a GxP-regulated pharmaceutical environment. This role involves authoring crucial validation documentation, mentoring teams on regulatory standards (including FDA, GAMP5, and 21 CFR Part 11), and maintaining strict adherence to Good Documentation Practices (GDP) throughout the validation lifecycle.
Roles & Responsibilities:
- Documentation Management: Draft, evaluate, and peer-review essential validation documentation in strict accordance with Good Documentation Practices (GDP).
- System Validation: Execute and oversee compliance and validation procedures specifically tailored for computerized systems.
- Team Mentorship: Coach and guide team members to ensure they fully grasp and consistently apply client workflows and project validation goals.
Professional & Technical Skills:
- Regulatory Knowledge: Expertise in Pharmaceutical Regulatory Compliance and Computerized System Validation (CSV).
- Industry Frameworks: Strong practical background in GxP environments, encompassing the complete validation lifecycle and the V-Model framework.
- Documentation Standards: Deep understanding and application of Good Documentation Practices (GDP).
- Compliance Guidelines: Thorough familiarity with GAMP5 industry standards and FDA regulatory guidelines.
- Project Lifecycle: Proven experience managing the end-to-end validation lifecycle for highly regulated projects.
- Communication & Analysis: Excellent analytical capabilities paired with strong interpersonal communication skills.
- Critical Thinking: Highly effective problem-solving and troubleshooting abilities.
Additional Information:
- Degree: Bachelor of Engineering (BE) degree or an equivalent academic credential.
- Core Competencies: CSV, General System Validation, FDA 21 CFR Part 11 compliance, and Computerized System Validation methodologies.
- The candidate should have minimum 5 years of experience
- This position is based at our Chennai office.
- A 15 years full time education is required.15 years full time education
About Accenture
Accenture is a leading global professional services company that helps the world’s leading businesses, governments and other organizations build their digital core, optimize their operations, accelerate revenue growth and enhance citizen services—creating tangible value at speed and scale. We are a talent- and innovation-led company with approximately 791,000 people serving clients in more than 120 countries. Technology is at the core of change today, and we are one of the world’s leaders in helping drive that change, with strong ecosystem relationships. We combine our strength in technology and leadership in cloud, data and AI with unmatched industry experience, functional expertise and global delivery capability. Our broad range of services, solutions and assets across Strategy & Consulting, Technology, Operations, Industry X and Song, together with our culture of shared success and commitment to creating 360° value, enable us to help our clients reinvent and build trusted, lasting relationships. We measure our success by the 360° value we create for our clients, each other, our shareholders, partners and communities.Visit us at www.accenture.com
Equal Employment Opportunity Statement
We believe that no one should be discriminated against because of their differences. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, military veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by applicable law. Our rich diversity makes us more innovative, more competitive, and more creative, which helps us better serve our clients and our communities.
Accenture Chennai, Tamil Nadu, IND Office
Chennai, India
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To locals, it's no secret that South India is leading the charge in big data infrastructure. While the environmental impact of data centers has long been a concern, emerging hubs like Chennai are favored by companies seeking ready access to renewable energy resources, which provide more sustainable and cost-effective solutions. As a result, Chennai, along with neighboring Bengaluru and Hyderabad, is poised for significant growth, with a projected 65 percent increase in data center capacity over the next decade.
