noida uttar pradesh regulatory affairs Jobs – 17 Open Jobs Today

Lead Consultant – Regulatory Affairs
Genpact India Pvt. Ltd. —Noida, Uttar Pradesh
- Full-time
- Hybrid work
- English
- Microsoft Office
- Master's degree
Quick apply
1h
Regulatory Affairs Executive
Accure Medical Pvt Ltd —Noida, Uttar Pradesh
- ₹12,000 - ₹16,000 a month
- Full-time
- Microsoft Word
- Microsoft Excel
- Bachelor's degree
Quick apply
5d
Regulatory Affairs Executive
Diligence Certifications —Noida, Uttar Pradesh
- ₹15,000 - ₹30,000 a month
- Full-time
- Microsoft Office
- Master's degree
- Bachelor's degree
- Paid time off
- Cell phone reimbursement
Quick apply
4d
Senior Manager - Regulatory Affairs CMC
Cencora —Noida, Uttar Pradesh
- Full-time
- Presentation skills
- Bachelor's degree
- Communication skills
Regulatory Affairs Executive
ACER BIOMEDICALS LLP —Noida, Uttar Pradesh
- ₹12,000 - ₹15,000 a month
- Full-time
- Microsoft Word
- Microsoft Excel
- Bachelor's degree
Quick apply
Regulatory Affairs Manager/Senior Manager-(EP)
Cencora —Noida, Uttar Pradesh
- Full-time
- Bachelor's degree
- Leadership
- Communication skills
Regulatory Affairs Manager / Senior Manager – EU Hub
Cencora —Noida, Uttar Pradesh
- Full-time
- Bachelor's degree
- Quality control
- Leadership
Analyst- Licensing & Registration
Ameriprise India —Noida, Uttar Pradesh
- Full-time
- Bachelor's degree
- Communication skills
- Work from home
Human Resources Manager
SSSi Online Tutoring Services —Noida, Uttar Pradesh
- Full-time
- Microsoft Powerpoint
- Project management
- Communication skills
Junior Research Fellow
Amity University —Noida, Uttar Pradesh
- ₹31,000 a month
- Email
- Research
- Master's degree
Team Lead – Regulatory & Sectoral Strategy
ICF —New Delhi District, Delhi
- Full-time
- Engineering
- Master's degree
- Bachelor's degree
General Compliance - Technical Filings ( FSSAI, MSME, GST)
Corpseed ITES Private Limited. —Noida, Uttar Pradesh
- ₹20,000 - ₹25,000 a month
- Urgently hiring
- Bachelor's degree
- In-person
- Cell phone reimbursement
Quick apply
2d
Regulatory Affair Sales Executive
Diligence Certifications —Noida, Uttar Pradesh
- ₹10,000 - ₹20,000 a month
- Full-time
- Bachelor's degree
- In-person
- Communication skills
Quick apply
Drug Registration Consultant
Professional Utilities —Nehru Place, Delhi, Delhi
- Up to ₹35,000 a month
- Full-time
- Bachelor's degree
- In-person
- Paid time off
- Paid sick time
Quick apply
Business Development Executive
MEDYUR PHARMACEUTICALS LIMITED —Noida, Uttar Pradesh
- ₹11,515.86 - ₹40,970.79 a month
- Full-time
- Sales
- Marketing
- English
- Health insurance
Quick apply
Admin Executive
Big Bee Consultant —Greater Noida, Uttar Pradesh
- ₹2,00,000 - ₹4,00,000 a year
- Microsoft Office
- Administrative experience
- Bachelor's degree

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Regulatory Affairs Executive
Accure Medical Pvt Ltd —Noida, Uttar Pradesh
The role is ideal for fresher or candidates with up to 2 years of experience who are eager to build a career in regulatory affairs within the medical device /…
₹12,000 - ₹16,000 a month
Quick apply
5d
Regulatory Affairs Executive
Diligence Certifications —Noida, Uttar Pradesh
2–3 years of relevant experience in Regulatory Affairs. Ensure compliance with applicable regulatory requirements and guidelines.
₹15,000 - ₹30,000 a month
Quick apply
4d

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Lead Consultant – Regulatory Affairs

Genpact India Pvt. Ltd. -
Noida, Uttar Pradesh

Quick apply

Job details

Full-time
1 hour ago

Qualifications

English
Microsoft Office
Master's degree
Project management
Quality assurance
Bachelor's degree
Data management
Mentoring
MA
Quality systems
BA
Communication skills
Information management

Full job description

Sr. Consultant - Regulatory Affairs

Ready to turn bold ideas into real-world impact?
At Genpact, we don’t just adapt to change, we lead it. AI and digital innovation are transforming the way businesses work, and we’re at the forefront of it. Genpact’s AI Gigafactory, our industry-first accelerator, exemplifies how we scale advanced technology solutions to help global enterprises work smarter, grow faster, and transform at scale. Whether tackling complex challenges through large-scale models or 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 agentic and advanced technology solutions company. We leverage process intelligence and artificial intelligence to deliver measurable outcomes. With a strong partner ecosystem and decades of client trust, we provide innovative solutions that transform how businesses run. Powered by a team with an active learning mindset and client centricity at its core, we deliver lasting value for the world’s leading enterprises.
Get to know us at genpact.com and on LinkedIn, YouTube, X, and Facebook.

Job Description

We are inviting applications for the role of lead Associate or lead Consultant Regulatory Affairs. Responsibilities: - Responsible for leading and executing CMC regulatory strategies for assigned postapproval pharmaceutical products in alignment with global regulations guidance and defined regulatory strategies including preparation and critical review of data and documents required for postapproval CMC submissions and lifecycle management. - Accountable for authoring reviewing and coordinating CMC documentation to support worldwide postapproval changes and lifecycle activities (variations supplements amendments) for commercial products under the strategic direction of senior regulatory CMC scientists or product leads. - Experienced in evaluating scientific and technical information to assess the merits and regulatory impact of proposed postapproval changes ensuring that rationales are clearly articulated riskbased and fully supported by appropriate data. - Able to prioritize plan and drive multiple CMC postapproval projects in parallel ensuring timely preparation review and submission of highquality dossiers in line with agreed project plans regulatory timelines and internal milestones. - Works effectively with crossfunctional teams (e.g. - QA QC manufacturing supply chain packaging device and analytics) to track and close out documentation gaps coordinate on change implementation status and provide clear concise regulatory updates to stakeholders through appropriate communication channels. - Demonstrates strong written and verbal communication skills including the ability to translate complex technical concepts into clear regulatory justifications and to influence decisionmaking in crossfunctional and global forums. - Shows sound understanding of related technical disciplines (such as pharmaceutical manufacturing analytical testing quality assurance and quality systems) and applies this knowledge when defining regulatory strategies and compiling CMC dossiers. - Proven ability to identify regulatory risks and opportunities generate innovative yet compliant solutions to issues and collaborate effectively with internal and external partners to align on regulatory pathways. - Active participation in departmental and crossfunctional continuous improvement initiatives such as enhancement of templates processes systems; - maintenance of standard operating procedures and internal guidelines etc. - Demonstrates flexibility and resilience in managing changing priorities unforeseen regulatory queries or health authority expectations and timesensitive projects while maintaining accuracy and compliance. - Exhibits strong leadership stakeholder management and interpersonal skills including mentoring junior colleagues and representing CMC regulatory function in project and governance meetings. - Possesses advanced working knowledge of MS Office and relevant regulatory/quality IT systems (e.g. - document management RIMS and tracking tools) to efficiently prepare manage and archive CMC regulatory documentation.

Qualifications

Bachelors - Health Administration, Bachelors - Healthcare, Bachelors - Pharmacy, Masters - Public Health, Masters - Regulatory Affairs

Certifications

Certified Compliance Officer (CCO) - VskillsVskills, Regulatory Affairs Certification (RAC) - UdemyUdemy

Required Skills

Change Management, Data Consulting, Data Management, Project Management, Quality Assurance (QA), Regulatory Affair Management, Regulatory Information Management, Strategic Planning

Language

English

Language Proficiency -

Proficient - C2

Additional Job Location -

Job Type

Regular

Master Skill List -

Regulatory Affairs - Practice

Remote Type -

Hybrid

Work Shift -

Day Job (India)

Why join Genpact?

Lead AI-powered transformation – Drive innovation and solve real-world business challenges that matter
Make an impact – Help global enterprises solve business challenges that matter
Accelerate your career – Gain hands-on experience, mentorship, and world-class learning opportunities to stay ahead
Work with the best – Join 140,000+ bold thinkers and problem-solvers who push boundaries every day
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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regulatory affairs jobs in noida uttar pradesh

Lead Consultant – Regulatory Affairs

Regulatory Affairs Executive

Regulatory Affairs Executive

Senior Manager - Regulatory Affairs CMC

Regulatory Affairs Executive

Regulatory Affairs Manager/Senior Manager-(EP)

Regulatory Affairs Manager / Senior Manager – EU Hub

Analyst- Licensing & Registration

Human Resources Manager

Junior Research Fellow

Team Lead – Regulatory & Sectoral Strategy

General Compliance - Technical Filings ( FSSAI, MSME, GST)

Regulatory Affair Sales Executive

Drug Registration Consultant

Business Development Executive

Admin Executive

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