Kandivali Mumbai Maharashtra Regulatory affairs specialist Jobs – 20 Open Jobs Today

Specialist - Regulatory Affairs - Operations 4B
Genpact India Pvt. Ltd. —Mumbai, Maharashtra
- Full-time
- Hybrid work
- Management
- English
- Master's degree
Quick apply
1d
Lead Associate – Regulatory Affairs
Genpact India Pvt. Ltd. —Mumbai, Maharashtra
- Full-time
- Hybrid work
- Medicine
- English
- Master's degree
Quick apply
Manager – Regulatory Affairs
Genpact India Pvt. Ltd. —Mumbai, Maharashtra
- Full-time
- Azure
- English
- Master's degree
Quick apply
QA Specialist
Sun Pharmaceutical Industries Ltd —Mumbai, Maharashtra
- Microsoft Excel
- English
- Windows
Regulatory Affairs – Chief Manager
Exeltis India —Mumbai, Maharashtra
- Email
- Master's degree
- Bachelor's degree
- APIs
Scientific Content Professionals – Physician Education
Centrix Healthcare Limited —Andheri West, Mumbai, Maharashtra
- ₹5,00,000 - ₹12,00,000 a year
- Full-time
- Medicine
- Master's degree
- Bachelor's degree
- Paid time off
- Paid sick time
Quick apply
6d
Copywriting Specialist
Accenture —Mumbai, Maharashtra
- Full-time
- Medicine
- English
- Analysis skills
Lead - Clinical Nutrition
Sun Pharma Laboratories Ltd —Mumbai, Maharashtra
- Weekend availability
- Doctoral degree
- Research
- Master's degree
AVP – Medical Strategy & Physician Education
Centrix Healthcare Limited —Andheri West, Mumbai, Maharashtra
- ₹15,00,000 - ₹30,00,000 a year
- Full-time
- Medicine
- Bachelor's degree
- In-person
- Paid time off
- Paid sick time
Quick apply
7d
Senior Specialist, Regulatory Affairs Manager EP
Cencora —Mumbai, Maharashtra
- Full-time
- Bachelor's degree
SE Asia & India MCO Rare Disease Medical Lead
Sanofi —Mumbai, Maharashtra
- Medicine
- Research
- Travel
13d
Senior Manager - Medical Affairs
Sun Pharmaceutical Industries Ltd —Mumbai, Maharashtra
- Weekend availability
- Research
- Analysis skills
- Travel
Medical Advisor - CVD
Sun Pharmaceutical Industries Ltd —Mumbai, Maharashtra
- Medicine
- Research
- Project management
VP ALCM - Partnering and Insight
HSBC Global Services Limited —Mumbai, Maharashtra
- Full-time
- Master's degree
- AI
3d
Veeva Publishing SME
Atos —Mumbai, Maharashtra
7d
Veeva Submission SME
Atos —Mumbai, Maharashtra
7d
Lead Associate -Regulatory Affairs'
Genpact India Pvt. Ltd. —Mumbai, Maharashtra
- Full-time
- English
- Master's degree
- Bachelor's degree
Quick apply

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Specialist - Regulatory Affairs - Operations 4B

Genpact India Pvt. Ltd. -
Mumbai, Maharashtra

Quick apply

Job details

Full-time
1 day ago

Qualifications

Management
English
Master's degree
Project management
Bachelor's degree
MA
Project implementation
BA

Full job description

Specialist - Regulatory Affairs - Operations

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

The Role demands for a demonstrated ability to execute responsibility in a highly regulated & process driven environment, the Person will be responsible for all the activities related to.
Manage and deliver end to end submissions for US, Europe, Canada, Japan, EAEU and ROW market in eCTD, NeeS and Paper format.
Act as liaison between the client and internal project team, Coordinating for routine regulatory submissions.
Provide timely invoices, project budget and keep visibility of overall financial health of engagement.
Manage the team by providing project management, prioritization, direction and leadership to team members in order to accomplish defined project deliverables on given deadlines.
Leverage subject matter knowledge on business / project implementation issues related to the Regulatory process.
Recruit new team members. Mentor for their growth.
Conduct Governance with the client and execute metrics compliance in the process.
Resolve technical, validation issues and provide guidance to team
Manage work triage and task allocation to ensure rapid turnaround for high-priority requests.
Monitor and report submissions activity, such as reporting volume, timelines, and quality metrics; informing future planning and forecasting activities; supporting overall regulatory intelligence.

Qualifications

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

Certifications

Certified Compliance Officer (CCO) - VskillsVskills, Certified Public Accountant (CPA) - Perfekt SzolnokPerfekt Szolnok, Certified Regulatory and Compliance Professional (CRCP) - JSS UniversityJSS University, Certified Regulatory Compliance Manager (CRCM) - The International Association of Risk and Compliance Professionals (IARCP)The International Association of Risk and Compliance Professionals (IARCP)

Required Skills

People Management, Project Management, Publishing, Submission Management

Language

English (Required)

Language Proficiency -

Proficient - C2

Additional Job Location -

Job Type

Regular

Master Skill List -

Regulatory Affairs - Operations

Remote Type -

Hybrid

Work Shift -

Evening 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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Refine Your Search

regulatory affairs specialist jobs in kandivali mumbai maharashtra

Specialist - Regulatory Affairs - Operations 4B

Lead Associate – Regulatory Affairs

Manager – Regulatory Affairs

QA Specialist

Regulatory Affairs – Chief Manager

Scientific Content Professionals – Physician Education

Copywriting Specialist

Lead - Clinical Nutrition

AVP – Medical Strategy & Physician Education

Senior Specialist, Regulatory Affairs Manager EP

SE Asia & India MCO Rare Disease Medical Lead

Senior Manager - Medical Affairs

Medical Advisor - CVD

VP ALCM - Partnering and Insight

Veeva Publishing SME

Veeva Submission SME

Lead Associate -Regulatory Affairs'

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