Regulatory Affairs Executive Vacancies at Piramal Pharma
- Piramal Critical Care Hiring Executive Labelling – Regulatory Affairs in Mumbai
- Company Overview
- Job Role & Responsibilities
- Executive Labelling – Regulatory Affairs Responsibilities
- Skills Required
- Eligibility / Qualifications
- Educational Qualification
- Experience Requirement
- Location & Salary
- Location
- Estimated Salary
- Application Process
- Apply Online
- Job ID
- Department
- Business Unit
- Application Deadline
- Frequently Asked Questions (FAQs)
- 1. What role is Piramal Critical Care hiring for?
- 2. Which qualifications are eligible for this pharmaceutical regulatory role?
- 3. What experience is required for this opportunity?
- 4. Which regulatory markets are preferred for this role?
- 5. What is the estimated salary for Executive Labelling roles?
- 6. What is the work location for this opportunity?
- Summary Table
Piramal Critical Care Hiring Executive Labelling – Regulatory Affairs in Mumbai
Piramal Critical Care has announced a new hiring opportunity for the position of Executive Labelling – Regulatory Affairs at its Kurla, Mumbai location. The company is inviting applications from experienced pharmaceutical regulatory affairs professionals with expertise in global labeling compliance, artwork management, regulatory submissions, and healthcare documentation.
This recruitment drive is attracting candidates searching for regulatory affairs jobs in Mumbai, pharma labelling specialist careers, global regulatory compliance jobs, artwork management vacancies, pharmaceutical labeling executive openings, USFDA regulatory affairs jobs, EU regulatory submission careers, and healthcare compliance opportunities.
Candidates with strong knowledge of global labeling regulations, pharmaceutical submissions, regulatory documentation, and compliance management can apply for this opportunity.
Company Overview
Piramal Critical Care (PCC), a business unit of Piramal Pharma, is one of the global leaders in inhaled anesthetics and hospital generic products. The company operates across more than 100 countries and provides critical care solutions for healthcare providers and patients worldwide.
PCC has strong expertise in inhalation anesthetics including Sevoflurane, Isoflurane, and Halothane, along with therapies related to spasticity management and hospital critical care products. The organization operates state-of-the-art manufacturing facilities in India and the United States, regularly inspected by global regulatory authorities including the US FDA and UK MHRA.
The pharmaceutical labeling and regulatory affairs sector continues to generate strong demand for professionals due to evolving global compliance standards, product lifecycle management requirements, labeling harmonization activities, and international healthcare regulations.
Mumbai remains one of India’s largest pharmaceutical and regulatory affairs hubs, creating strong career opportunities in global labeling operations, healthcare compliance, artwork management, regulatory submissions, and pharmaceutical documentation management.
Job Role & Responsibilities
Executive Labelling – Regulatory Affairs Responsibilities
Candidates selected for this role will support global labeling operations and regulatory compliance activities for Piramal Critical Care products.
Key responsibilities include:
- Managing artworks and labeling components for global pharmaceutical products
- Ensuring compliance with global labeling regulations and GMP standards
- Supporting label evaluations, maintenance, reviews, and approvals
- Coordinating with cross-functional teams for regulatory submissions
- Preparing labeling documents including SmPC, PIL, and labeling texts for EU submissions
- Supporting timely labeling approvals and query resolution activities
- Proofreading label copies and annotation documents for accuracy
- Creating SPL for US human and veterinary product submissions
- Supporting annual drug listing and establishment registration activities
- Monitoring innovator labeling updates for generic products
- Performing side-by-side comparison with RLD labeling requirements
- Coordinating CCDS development and labeling updates
- Supporting promotional material review and labeling compliance
- Maintaining centralized repositories for labeling documentation
- Coordinating with health authorities, CMOs, distributors, and external stakeholders
Skills Required
Candidates should possess:
- Strong regulatory affairs and labeling knowledge
- Global pharmaceutical labeling compliance expertise
- Artwork management and proofreading skills
- Knowledge of EU and US regulatory submission requirements
- SPL creation and labeling documentation expertise
- GMP and healthcare compliance understanding
- Project management and coordination skills
- Communication and stakeholder management abilities
- Organizational and documentation management skills
- Attention to detail and analytical abilities
Candidates with exposure to USFDA, EU, MHRA, and Rest of World regulatory markets will have an advantage.
Eligibility / Qualifications
Educational Qualification
Candidates with pharmaceutical educational backgrounds are eligible.
Relevant educational qualifications include:
B.Pharm, M.Pharm, Pharmaceutical Sciences, Regulatory Affairs, Clinical Research, Healthcare Compliance.
Experience Requirement
- Minimum 4 years of regulatory affairs experience
- Global regulatory experience preferred
- US, EU, and Rest of World labeling experience preferred
- Experience in labeling compliance and regulatory documentation preferred
- Artwork management and submission experience preferred
These openings are suitable for:
- Regulatory affairs executives
- Global labeling specialists
- Pharmaceutical compliance professionals
- Artwork and labeling associates
- Regulatory documentation specialists
- Healthcare compliance professionals
- USFDA and EU regulatory affairs candidates
Location & Salary
Location
Kurla, Mumbai
Estimated Salary
₹7 LPA – ₹14 LPA approximately
Salary may vary depending on global regulatory experience, labeling expertise, artwork management exposure, and healthcare compliance knowledge.
Application Process
Interested candidates can apply through the official Piramal Pharma careers portal.
Apply Online
Job ID
R00002017
Department
Regulatory Affairs
Business Unit
Piramal Critical Care
Application Deadline
24 June 2026
Frequently Asked Questions (FAQs)
1. What role is Piramal Critical Care hiring for?
Piramal Critical Care is hiring for the position of Executive Labelling – Regulatory Affairs.
2. Which qualifications are eligible for this pharmaceutical regulatory role?
Candidates with B.Pharm, M.Pharm, Pharmaceutical Sciences, and Regulatory Affairs qualifications can apply.
3. What experience is required for this opportunity?
Candidates with at least 4 years of regulatory affairs and global labeling experience are preferred.
4. Which regulatory markets are preferred for this role?
Experience in US, EU, and major Rest of World regulatory markets is preferred.
5. What is the estimated salary for Executive Labelling roles?
The expected salary range is approximately ₹7 LPA to ₹14 LPA depending on regulatory expertise and global labeling experience.
6. What is the work location for this opportunity?
The work location is Kurla, Mumbai.
Summary Table
| Company | Piramal Critical Care |
|---|---|
| Department Vacancies | Executive Labelling – Regulatory Affairs |
| Qualification | B.Pharm, M.Pharm, Pharmaceutical Sciences, Regulatory Affairs |
| Experience | 4 Years Regulatory Affairs Experience |
| Location | Kurla, Mumbai |
To apply for this job please visit piramalpharma.wd102.myworkdayjobs.com.
