At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials and bring life-changing therapies to patients in need worldwide.
We are seeking a Senior Validation and Compliance Lead (India) to join our A-team (hybrid*). As a Senior Validation and Compliance Lead will be responsible for leading the Validation and Compliance activities within Technology & Innovation assigned projects at Allucent. This position controls and monitors the Validation and Compliance status of GxP impacting systems, ensures planning, preparation, and execution of validation and testing activities in accordance with standard operating procedures, regulatory guidelines, executed client contracts, and clients’ expectations.
In this role you key task will include:
Disclaimers:
*Our hybrid work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our global offices.
“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”
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At Allucent™, we’re genuinely excited to expand our A-team with a Senior Validation and Compliance Lead. This role is crucial as you will guide the Validation and Compliance activities for various Technology & Innovation projects, ensuring we stay ahead of the curve in the intricate world of clinical trials. Your day-to-day will involve overseeing GxP systems to ensure they meet rigorous standards, from documentation to hands-on staff training. You’ll work closely with IT and Quality Assurance teams to weave validated systems into our operations seamlessly. The role isn’t just about compliance; it’s also about being proactive, identifying risks, and suggesting process improvements. You’ll participate in audits, refine our practices, and maintain the highest quality and regulatory standards. We value continuous improvement, so your insights into tech advancements and regulatory updates will be welcomed. If you come with at least five years of experience in computerized system validation, coupled with a degree in Computer Science, Life Sciences, or a related field, you’re on the right track! We prioritize building durable relationships with our clients, so strong communication and analytical skills are essential. Additionally, our hybrid working policy allows for flexibility, ensuring that you can balance work and life effectively. Join Allucent, where your contributions matter, and you have the opportunity to grow your career while making a real impact in the biopharmaceutical field!
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