▷ (Urgent Search) Lead Consultant - Regulatory Affairs
3 weeks ago
Ready to build the future with AI At Genpact we don t just keep up with technology we set the pace AI and digital innovation are redefining industries and we re leading the charge Genpact s AI Gigafactory our industry-first accelerator is an example of how we re scaling advanced technology solutions to help global enterprises work smarter grow faster and transform at scale From large-scale models to agentic AI our breakthrough solutions tackle companies most complex challenges If you thrive in a fast-moving innovation-driven environment love building and deploying cutting-edge AI solutions and want to push the boundaries of what s possible this is your moment Genpact NYSE G is an advanced technology services and solutions company that delivers lasting value for leading enterprises globally Through our deep business knowledge operational excellence and cutting-edge solutions - we help companies across industries get ahead and stay ahead Powered by curiosity courage and innovation our teams implement data technology and AI to create tomorrow today Get to know us at genpact com and on LinkedIn X YouTube and Facebook Inviting applications for the role of Management Trainee Assistant Manager- Lead Associate or Lead Consultant Regulatory affairs Responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations guidance and defined regulatory strategies along with the preparation and review of information required for development of regulatory CMC dossiers for commercial products Responsibilities The core responsibility will be to review the authored documents compare them with source documents ensure there are no transcription or formatting errors no quality errors and ensure compliance with regulatory guidelines Maintaining the quality of documents through quality reviews ensuring No Queries received from Health Authorities Work on authoring CMC documentation for worldwide marketing of pharmaceutical products for initial registration and life-cycle management under the direction of team scientists Experience in reviewing scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data Able to prioritize execute the project according to the project plan timelines schedules Work with cross-functional teams to track and follow up outstanding documentation coordinate on project status reporting to stakeholders using different communication channels Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner Strong listening skills Demonstrated understanding of related fields e g pharmaceutical manufacturing analytical testing and quality assurance Ability to generate innovative solutions to problems and effectively collaborate with and communicate with key stakeholders Active participation in departmental improvement activities such as system modifications maintenance of standard operating procedures internal guidelines etc Demonstrated flexibility in responding to changing priorities multi-tasking and dealing with unexpected events Effective leadership communication and interpersonal skills Advanced knowledge of MS Office Superior attentiveness to detail has a strong regulatory background Qualifications we seek in you Bachelor s or master s degree required in science engineering or related field advanced degree preferred Why join Genpact Lead AI-first transformation - Build and scale AI solutions that redefine industries Make an impact - Drive change for global enterprises and solve business challenges that matter Accelerate your career Gain hands-on experience world-class training mentorship and AI certifications to advance your skills Grow with the best - Learn from top engineers data scientists and AI experts in a dynamic fast-moving workplace Committed to ethical AI - Work in an environment where governance transparency and security are at the core of everything we build Thrive in a values-driven culture - Our courage curiosity and incisiveness - built on a foundation of integrity and inclusion - allow your ideas to fuel progress Come join the 140 000 coders tech shapers and growth makers at Genpact and take your career in the only direction that matters Up Let s build tomorrow together Genpact is an Equal Opportunity Employer and considers applicants for all positions without regard to race color religion or belief sex age national origin citizenship status marital status military veteran status genetic information sexual orientation gender identity physical or mental disability or any other characteristic protected by applicable laws Genpact is committed to creating a dynamic work environment that values respect and integrity customer focus and innovation Furthermore please do note that Genpact does not charge fees to process job applications and applicants are not required to pay to participate in our hiring process in any other way Examples of such scams include purchasing a starter kit paying to apply or purchasing equipment or training
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Officer - Regulatory Affairs
2 days ago
Lucknow, Uttar Pradesh, India Geetank Pharmaceutical pvt ltd Full timeGeetank Pharmaceutical Pvt. Ltd. URGENT REQUIREMENT MALE CANDIDATE. POST- OFFICER REGULATORY AFFAIRS RESPONSIBILITIES- 1.DOSSIER 2.REVIEW 3.QUERY SOLVED QUALIFICATION- B PHARMA EXPERIENCE - MIN 02 YEAR (QA, RA ) SALARY - 12 K TO 16 K OFFICE TIME -10:00AM TO 6:00 PM INTERVIEW TIME- 11:00 AM TO 5:00PM CALLING TIME -10:00AM TO 6:00PM PRIYANKA...
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senior drug regulatory affairs executive
1 week ago
Lucknow, Uttar Pradesh, India Geetank Pharmaceutical Pvt. Ltd. Full time ₹ 1,44,000 - ₹ 2,04,000 per yearGeetank Pharmaceutical Pvt. Ltd.Urgent Requirement only male candidate .post- senior drug regulatory affairs executivequalification- B pharmaexperience – only Drug regulatory affairs experience 1 year ( Dossier Preparation and dossier review CTD & ACTD )salary – 12 k to 17 kOffice time -10:00 am to 6:00 pmInterview Time- 11:00 am to 5:00 pmCalling Time...
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Regulatory Affairs Executive
15 hours ago
Noida, Uttar Pradesh, India Diligence Certification Full timeJob Summary: Key Responsibilities: Prepare, review, and maintain regulatory submissions and documentation. Communicate with clients and regulatory authorities for updates and approvals. Ensure compliance with all relevant regulations, standards, and guidelines. Maintain accurate records of communications, approvals, and submissions. Support internal...
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Regulatory Affairs Executive
15 hours ago
Noida, Uttar Pradesh, India diligence certifications Full time**Job Summary**: **Key Responsibilities**: - Prepare, review, and maintain regulatory submissions and documentation. - Communicate with clients and regulatory authorities for updates and approvals. - Ensure compliance with all relevant regulations, standards, and guidelines. - Maintain accurate records of communications, approvals, and submissions. -...
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Drug Regulatory Affairs Executive
2 weeks ago
Lucknow, India Lucent Biotech Ltd. Full timeLucent Biotech Limited company Hiring For **Drug Regulatory Affairs Executive.** **Regulatory affairs officers ensure the appropriate licensing, marketing and legal compliance of a range of pharmaceutical and medical products in order to control their safety and efficacy** As a regulatory affairs officer you'll be the crucial link between your company, its...
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Regulatory Affairs Specialist
7 days ago
uttar pradesh, India Shiv Nadar School Full timeJob Title: Senior Manager – Regulatory Affairs & Legal CompliancesLocation: Core Office, NoidaEmployment Type: Full-timeJob Summary:We are seeking a detail-oriented and proactive professional to oversee the organization’s legal, regulatory, and compliance functions. The incumbent will be responsible for ensuring adherence to statutory requirements,...
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Regulatory Affairs Specialist
5 days ago
uttar pradesh, India Shiv Nadar School Full timeJob Title: Senior Manager – Regulatory Affairs & Legal Compliances Location: Core Office, Noida Employment Type: Full-time Job Summary: We are seeking a detail-oriented and proactive professional to oversee the organization’s legal, regulatory, and compliance functions. The incumbent will be responsible for ensuring adherence to statutory requirements,...
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Manager - Regulatory Affairs
3 weeks ago
Lucknow, Uttar Pradesh, India GENPACT Full timeReady to build the future with AI At Genpact we don t just keep up with technology we set the pace AI and digital innovation are redefining industries and we re leading the charge Genpact s AI Gigafactory our industry-first accelerator is an example of how we re scaling advanced technology solutions to help global enterprises work smarter grow faster and...
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Regulatory Affairs Associate
6 days ago
Ghaziabad, Uttar Pradesh, India Shredwolf Incorporation Full time**Role Overview** We are seeking a detail-oriented and proactive **Regulatory Documentation Associate** to support the preparation, review, and submission of documents for regulatory approvals with authorities such as **CDSCO, BIS, FSSAI**, and other relevant bodies. The role involves managing documentation processes, ensuring compliance with regulatory...
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Senior Regulatory Affairs Trainer
4 weeks ago
Guntur, Andhra Pradesh, India, Andhra Pradesh Tek Support Part timeJob Title: Regulatory AffairsLocation: RemoteJob type: Part-timeJob Summary:We are seeking a highly experienced Regulatory Affairs Trainer with over 10 years of expertise in global regulatory compliance, submissions, and lifecycle management across medical devices, pharmaceuticals, biotech, and FMCG sectors. The trainer will be responsible for designing and...