Dadar Mumbai Maharashtra Consultant – regulatory affairs Jobs – 14 Open Jobs Today

Regulatory Affairs Associate
Pharmanovia —Mumbai, Maharashtra
- Full-time
- Remote
- Bachelor's degree
Lead Consultant – Regulatory Affairs
Genpact India Pvt. Ltd. —Mumbai, Maharashtra
- Full-time
- Hybrid work
- English
- Microsoft Office
- Master's degree
Quick apply
Manager - Regulatory Affairs
Samarth Life Sciences —Goregaon, Mumbai, Maharashtra
- ₹6,00,000 - ₹8,00,000 a year
- Full-time
- Bachelor's degree
- In-person
- Health insurance
- Flexible schedule
Quick apply
Manager - Regulatory Affairs
Samarth life sciences PVT LTD —Mumbai, Maharashtra
- ₹4,50,000 - ₹8,00,000 a year
- Full-time
- B.Sc
- Master's degree
- Bachelor's degree
- Flexible schedule
Quick apply
Regulatory & Compliance Associate. Skyleaf consultants
Skyleaf Consultants —Mumbai, Maharashtra
- ₹8,00,000 - ₹10,00,000 a year
- Full-time
- Research
- Communication skills
Executive Regulatory Affair
Ascent Meditech —Goregaon, Mumbai, Maharashtra
- B.Sc
- Master's degree
- Bachelor's degree
Liasoning Officer
VIVAAN WATER & ENVIRO SOLUTIONS PVT. LTD. —Vileparle, Mumbai, Maharashtra
- ₹40,000 - ₹50,000 a month
- Full-time
- Microsoft Excel
- Microsoft Office
- Bachelor's degree
Quick apply
5d
Company Secretary & Compliance Officer
Dear Shadow —Vikhroli, Mumbai, Maharashtra
- ₹8,00,000 - ₹10,00,000 a year
- Full-time
- Microsoft Office
- Master's degree
- In-person
Quick apply
Liaison Manager
Vivaan Water & Enviro Solutions Pvt. Ltd. —Mumbai, Maharashtra
- ₹30,000 - ₹50,000 a month
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Head of Exports
Oh!G snack —Mumbai, Maharashtra
- ₹40,000 - ₹80,000 a month
- Full-time
- Master's degree
- Bachelor's degree
- Travel
Quick apply
Graduate Trainee
Russell Investments —Mumbai, Maharashtra
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Legal Manager
Man Investment Services —Mumbai, Maharashtra
- ₹4,00,000 - ₹6,00,000 a year
- Full-time
- English
- Analysis skills
- Bachelor's degree
Quick apply
8d
Company Secretary - M1
LenDenClub —Mumbai, Maharashtra
- Microsoft Office
- Master's degree
- Communication skills
Quick apply
14d
Legal Manager Leading indian fashion retail pioneer
Skyleaf Consultants —Mumbai, Maharashtra
- ₹15,00,000 - ₹20,00,000 a year
- Full-time

More jobs to discover

Find similar jobs that you might be interested in.

Lead Consultant – Regulatory Affairs
Genpact India Pvt. Ltd. —Mumbai, Maharashtra
Experienced in evaluating scientific and technical information to assess the merits and regulatory impact of proposed post approval changes ensuring that…
Quick apply
Head of Exports
Oh!G snack —Mumbai, Maharashtra
The *Head – Exports* will be responsible for driving the Company's international business growth by developing new export markets, appointing distributors and…
₹40,000 - ₹80,000 a month
Quick apply

I want to receive the latest job alerts for consultant – regulatory affairs in dadar 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

consultant – regulatory affairs jobs near dadar mumbai maharashtra

Legal Manager jobs in Mumbai, Maharashtra

Compliance Consultant jobs in Mumbai, Maharashtra

Regulatory Affairs Specialist jobs in Mumbai, Maharashtra

Secretary jobs in Mumbai, Maharashtra

Liaison jobs in Mumbai, Maharashtra

Legal Officer jobs in Jharkhand

Legal Manager jobs in Vashi, Navi Mumbai, Maharashtra

Government Legal jobs in Ahmedabad, Gujarat

Legal Manager jobs in Kerala

Legal Manager jobs in West Bengal

Sales Manager jobs in Aurangabad, Maharashtra

Legal Manager jobs in Ghaziabad, Uttar Pradesh

Retainer Advocate, Legal Consultant jobs in Mumbai, Maharashtra

Compliance Consultant jobs in Gurgaon, Haryana

Compliance Broking jobs in Gujarat

Compliance Consultant jobs in Delhi

Compliance Consultant jobs in Kochi, Kerala

Travel Consultant jobs in Mohali, Punjab

Regulatory Affairs Specialist jobs in Kochi, Kerala

Regulatory Affairs Specialist jobs in Dehradun, Uttarakhand

Regulatory Affairs Associate

Pharmanovia -
Mumbai, Maharashtra

Apply Now

Job details

Full-time

Qualifications

French
Clinical research
Bachelor's degree
Technical writing
Document management systems
Italian
Information management
German
Product lifecycle management

Full job description

Regulatory Affairs Associate – Full Time – Hybrid – Based in Mumbai or Vadodara – (3 days in the office and two days working from home)

About the Company

Pharmanovia is a dynamic, fast-growing international pharmaceutical company with a portfolio of over 20 brands across more than 140 markets. Our mission is to improve patient health globally by revitalising niche, tried-and-trusted medicines. Since its inception in 2013, Pharmanovia has grown consistently year on year, focusing on delivering high-quality branded prescription medicines to patients, prescribers, and healthcare providers worldwide. Our growth has enabled the company to reinvest in its products, brands, people, and communities. Today, Pharmanovia employs more than 300 colleagues representing 29 nationalities and operates across Europe, the Middle East, Asia-Pacific, and Latin America. Our core therapeutic areas include Cardiovascular, Oncology, Endocrinology, and Neurology. We are an agile, entrepreneurial, and innovative speciality pharmaceutical company committed to maximising the value of established and speciality medicines while improving patient access worldwide.

About the Role

We are seeking a Regulatory Affairs Associate to join our growing Global Regulatory Affairs team. This is an excellent opportunity for a regulatory professional with experience in product labelling, lifecycle management and global regulatory processes to contribute to a diverse international portfolio. You will support global regulatory activities, product information maintenance, labelling compliance, and regulatory submissions, while collaborating closely with Regulatory Affairs, Pharmacovigilance, Artwork, Supply Chain, and external partners worldwide. The successful candidate will play a key role in ensuring regulatory compliance, maintaining accurate product information, supporting global labelling strategies and driving timely implementation of regulatory changes across international markets.

Responsibilities

Supporting the development, maintenance and implementation of global product labelling strategies, including CCDS, SmPCs, package inserts and associated patient information documents.
Preparing, reviewing and maintaining global and regional product information documentation to ensure compliance with applicable regulatory requirements.
Managing global labelling updates and lifecycle maintenance activities across multiple international markets.
Reviewing prescribing information, patient information leaflets and product labelling for Europe, North America, Australia and key emerging markets.
Preparing and managing regulatory documentation to support product information variations, updates and submissions.
Acting as a key contributor to Labelling Committee activities, including preparation, review and presentation of supporting documentation.
Maintaining accurate product information records within regulatory information management systems (RIMS) and electronic document management systems (eDMS).
Ensuring timely implementation and communication of approved labelling changes to internal and external stakeholders.
Supporting the preparation, review and quality control of regulatory submission packages and associated documentation.
Reviewing and approving artwork and packaging components to ensure alignment with approved product information.
Working closely with global affiliates, distributors, consultants and health authorities to support regulatory submissions and product maintenance activities.
Monitoring regulatory developments and communicating regulatory risks, requirements and mitigation strategies to project teams and stakeholders.

Qualifications

Bachelor’s degree in a scientific, pharmaceutical, healthcare or life sciences discipline.

Required Skills

Experience within Regulatory Affairs, Regulatory Labelling, Medical Affairs, Pharmacovigilance, Clinical Research or a related pharmaceutical function.
Strong experience supporting global product labelling activities, including CCDS, SmPC updates, package inserts and artwork approval processes.
Good understanding of global regulatory labelling requirements and lifecycle management processes.
Experience maintaining product information and regulatory documentation across international markets.
Knowledge of regulatory submission structures and content, including MAA, NDA and lifecycle maintenance submissions.
Familiarity with EU regulatory requirements, guidelines and regulatory procedures.
Experience working with Regulatory Information Management Systems (RIMS) and electronic document management systems (eDMS).
Ability to review complex regulatory documents for accuracy, consistency and compliance.
Strong scientific and technical writing skills.
Excellent attention to detail with proven ability to identify inconsistencies and mitigate compliance risks.

Preferred Skills

Experience supporting global labelling governance processes.
Experience with product lifecycle management in international markets.
Additional language skills, particularly German, Italian or French.
Experience within speciality pharmaceuticals, branded medicines or multinational pharmaceutical organisations.

Pay range and compensation Package

We offer a competitive salary plus a bonus and rewards package, including holidays, employee recognition awards, social events, a pension scheme, and hybrid Working

Equal Opportunity Statement

Pharmanovia is an equal-opportunity employer. Pharmanovia does not unlawfully discriminate against employees or applicants for employment based on an individual’s race, colour, religion, creed, sex, sexual orientation, gender identity or expression, national origin, genetic information, age, disability, marital status or any other status protected by applicable law. This policy applies to all terms, conditions, and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. Pharmanovia will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Apply Now

Refine Your Search

consultant – regulatory affairs jobs in dadar mumbai maharashtra

Regulatory Affairs Associate

Lead Consultant – Regulatory Affairs

Manager - Regulatory Affairs

Manager - Regulatory Affairs

Regulatory & Compliance Associate. Skyleaf consultants

Executive Regulatory Affair

Liasoning Officer

Company Secretary & Compliance Officer

Liaison Manager

Head of Exports

Graduate Trainee

Legal Manager

Company Secretary - M1

Legal Manager Leading indian fashion retail pioneer

More jobs to discover

I want to receive the latest job alerts for consultant – regulatory affairs in dadar mumbai maharashtra

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected