Mira Road Mumbai Maharashtra Regulatory affairs specialist Jobs – 13 Open Jobs Today

Specialist - Regulatory Affairs - Operations 4A
Genpact India Pvt. Ltd. —Mumbai, Maharashtra
- Full-time
- Hybrid work
- English
- Microsoft Office
- Master's degree
Quick apply
8d
Sr. Specialist - Regulatory Affairs - Operations 4C
Genpact India Pvt. Ltd. —Mumbai, Maharashtra
- Full-time
- Hybrid work
- English
- Microsoft Office
- Master's degree
Quick apply
8d
Specialist Regulatory Affairs LCM - Strategic Growth Products
Advanz Pharma —Andheri, Mumbai, Maharashtra
- Master's degree
- Bachelor's degree
- Agile
- Health insurance
- Work from home
Specialist - Product information Specialist
Orion Corporation —Mumbai, Maharashtra
- Email
- Hybrid work
- Microsoft Word
- Word processing
- Master's degree
Regulatory Affairs – Chief Manager
Exeltis India —Mumbai, Maharashtra
- Email
- Master's degree
- Bachelor's degree
- APIs
Associate- Product Intelligence
Azelis —Mumbai, Maharashtra
- Night shift
- CRM software
- Microsoft Excel
- Customer service
Copywriting Specialist
Accenture —Mumbai, Maharashtra
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Medicine
Sr. Technical Specialist (175411)
Colgate-Palmolive —Mumbai, Maharashtra
- Microsoft Access
- Computer Science
- Software troubleshooting
Lead Analyst - Process Analytics - Supply Chain - Procurement 4D
Genpact India Pvt. Ltd. —Mumbai, Maharashtra
- Full-time
- Hybrid work
- Computer Science
- English
- Research
Quick apply
Senior Manager - Medical Affairs
Sun Pharmaceutical Industries Ltd —Mumbai, Maharashtra
- Weekend availability
- Research
- Analysis skills
- Travel
VP ALCM - Partnering and Insight
HSBC Global Services Limited —Mumbai, Maharashtra
- Full-time
- Master's degree
- AI
National Sales Manager
Arkon Solution LLP —Mumbai, Maharashtra
- ₹15,00,000 - ₹25,00,000 a month
- Full-time
- Medicine
- Sales
- Master's degree
- Health insurance
- Paid time off
Quick apply
9d

More jobs to discover

Find similar jobs that you might be interested in.

Sr. Specialist - Regulatory Affairs - Operations 4C
Genpact India Pvt. Ltd. —Mumbai, Maharashtra
Collaborate effectively with cross‑functional teams (e.g., QA, QC, manufacturing, supply chain, packaging, device, and analytics), CMOs, and external partners…
Quick apply
8d

I want to receive the latest job alerts for regulatory affairs specialist in mira road mumbai maharashtra

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

regulatory affairs specialist jobs near mira road mumbai maharashtra

Copywriter jobs in Mumbai, Maharashtra

Regulatory Affairs Specialist jobs in Mumbai, Maharashtra

Vice President jobs in Mumbai, Maharashtra

Supply Chain Analyst jobs in Mumbai, Maharashtra

Associate Product Owner jobs in Mumbai, Maharashtra

Regulatory Affairs Manager jobs in Mumbai, Maharashtra

Email Copywriter jobs in Mumbai, Maharashtra

Copywriter jobs in Kochi, Kerala

Copywriter jobs in Surat, Gujarat

Freelance Copywriter jobs in Remote

Junior Copywriter jobs in Mumbai, Maharashtra

Copywriter ₹1,50,000 jobs in Remote

Copywriter jobs in Marathahalli, Bengaluru, Karnataka

Regulatory Affairs Specialist jobs in Ahmedabad, Gujarat

Regulatory Affairs Specialist jobs in Race Course, Vadodara, Gujarat

Regulatory Affairs Specialist jobs in Patan, Gujarat

Ministry Of Home Affairs, Govt Of India jobs in Bengaluru, Karnataka

Regulatory Affairs Specialist jobs in Kochi, Kerala

Vice President jobs in Sanand, Ahmedabad, Gujarat

Teacher, Admin, Principal, Vice Principal jobs in Bhatinda, Punjab

Specialist - Regulatory Affairs - Operations 4A

Genpact India Pvt. Ltd. -
Mumbai, Maharashtra

Quick apply

Job details

Full-time
8 days ago

Qualifications

Power BI
SAP
English
Microsoft Office
Master's degree
Quality assurance
Bachelor's degree
Quality control
MA
QA/QC
BA
Communication skills

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

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 of small molecules/ pharma, large molecules/ biologicals, etc.
Work on authoring CMC documentation for worldwide marketing of pharmaceutical products for initial registration and life-cycle management submissions under 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.
Understanding of job responsibilities & processes of cross-functional teams, manufacturing sites, Quality Assurance, Quality control, etc. Prior experience in these departments is preferable.
Experience in RA/ QA/ QC system and tools like SAP, documentum, Veeva, LIMS, spotfire, Power BI, etc is preferrable.
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 to 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.

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

Pharmaceutical Regulatory Affairs

Language

English (Required)

Language Proficiency -

Proficient - C2

Additional Job Location -

Job Type

Regular

Master Skill List -

Regulatory Affairs - Operations

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.

Quick apply

Refine Your Search

regulatory affairs specialist jobs in mira road mumbai maharashtra

Specialist - Regulatory Affairs - Operations 4A

Sr. Specialist - Regulatory Affairs - Operations 4C

Specialist Regulatory Affairs LCM - Strategic Growth Products

Specialist - Product information Specialist

Regulatory Affairs – Chief Manager

Associate- Product Intelligence

Copywriting Specialist

Sr. Technical Specialist (175411)

Lead Analyst - Process Analytics - Supply Chain - Procurement 4D

Senior Manager - Medical Affairs

VP ALCM - Partnering and Insight

National Sales Manager

More jobs to discover

I want to receive the latest job alerts for regulatory affairs specialist in mira road mumbai maharashtra

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected