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Junior Quality Analyst
1 month ago
ValGenesis is an equal opportunity employer and remuneration to commensurate based on experience and competency and will be in par with the best in industry.
- Overall change and review responsibility for Quality Management Processes in line with the standard requirements of ISO 9001:2015 and ISO: 27001:2013.
- Knowledge of Risk-Based Approach to Compliant GxP Computerized Systems - GAMP 5 that would aid in facing customer audits
- Support the product development life cycle for computerized systems with change controls, deviations management ensuring that relevant documentation is in place and maintained according to the ValGenesis requirements.
- Understanding of computerized systems validation, lifecycle management and 21 CFR Part 11 requirements.
- Conduct and manage the internal audits including vendor audits and report to Head of Quality / Management
- Customer focus with eye for details, analysis and continual improvements.
- Managing with day to day quality control activities are as per quality plan requirements and track them to closure.
- Up to date with the latest development of the standards and other regulatory needs in the pharmaceutical industry and maintain compliance to the QMS.
- To review and approve the various validation documents both internally as well as during product deployment for customers. The documents are routed in a workflow with predefined SLA and the expectation is to review thoroughly without any defects or missing content.
- Support on Information Security Management System in terms of review of documents and ensure that is line with the requirements of security standards.
- Improve compliance through continual improvement programs across the organization and Quality by design.
- Support training department in terms of training plan, conduct of training and management for the ValGenesis.
- Improve compliance through continual improvement programs across the organization and Quality by design.
- Support on Information Security Management System in terms of review of documents and ensure that is line with the requirements of security standards.
- To review and approve the various validation documents both internally as well as during product deployment for customers. The documents are routed in a workflow with predefined SLA and the expectation is to review thoroughly without any defects or missing content.
- Up to date with the latest development of the standards and other regulatory needs in the pharmaceutical industry and maintain compliance to the QMS.
- Managing with day to day quality control activities are as per quality plan requirements and track them to closure.
- Customer focus with eye for details, analysis and continual improvements.
- Conduct and manage the internal audits including vendor audits and report to Head of Quality / Management
- Understanding of computerized systems validation, lifecycle management and 21 CFR Part 11 requirements.
- Support the product development life cycle for computerized systems with change controls, deviations management ensuring that relevant documentation is in place and maintained according to the ValGenesis requirements.
- Knowledge of Risk-Based Approach to Compliant GxP Computerized Systems - GAMP 5 that would aid in facing customer audits
Requirements
- Engineering Graduate or a Pharma Graduate with a good understanding about SDLC.
- Prefer CBSC education with a good knowledge of computers and programming.
- Knowledge of testing and validation and quality is preferred.
- Knowledge of Information Security and associated functions is preferred.
- Excellent communication skills (Both written and oral)
- Customer Management and inter personal Skills.
- Self-starter, well organized and self-motivated.
- Strong analytical and project management skills.
- Confident and dynamic personality.
- Attitude to learn and perform new areas including life sciences domain, Cloud, product development and other support functions
Preferred Skills- Presentation skills.
- Knowledge of using computers, programming concepts and software engineering.
- Attitude to learn and perform new areas including life sciences domain, Cloud, product development and other support functions
- Confident and dynamic personality.
- Strong analytical and project management skills.
- Self-starter, well organized and self-motivated.
- Customer Management and inter personal Skills.
- Excellent communication skills (Both written and oral)
- Knowledge of Information Security and associated functions is preferred.
- Knowledge of testing and validation and quality is preferred.
- Prefer CBSC education with a good knowledge of computers and programming.
Benefits
We're on a Mission
In 2005, we disrupted the life sciences industry by introducing the world's first digital validation lifecycle management system. ValGenesis VLMS revolutionized compliance-based corporate validation activities and has remained the industry standard.
Today, we continue to push the boundaries of innovation ― enhancing and expanding our portfolio beyond validation with an end-to-end digital transformation platform. We combine our purpose-built systems with world-class consulting services to help every facet of GxP meet evolving regulations and quality expectations.
The Team You'll Join
- Our customers' success is our success. We keep the customer experience centered in our decisions, from product to marketing to sales to services to support. Life sciences companies exist to improve humanity's quality of life, and we honor that mission.
- We work together. We communicate openly, support each other without reservation, and never hesitate to wear multiple hats to get the job done.
- We think big. Innovation is the heart of ValGenesis. That spirit drives product development as well as personal growth. We never stop aiming upward.
- We're in it to win it. We're on a path to becoming the number one intelligent validation platform in the market, and we won't settle for anything less than being a market leader.
How We Work
Our Chennai and Bangalore offices are onsite, 5 days per week. We believe that in-person interaction and collaboration fosters creativity, and a sense of community, and is critical to our future success as a company.
ValGenesis is an equal-opportunity employer that makes employment decisions on the basis of merit. Our goal is to have the best-qualified people in every job. All qualified applicants will receive consideration for employment without regard to race, religion, sex, sexual orientation, gender identity, national origin, disability, or any other characteristics protected by local law.
