Glenmark Pharmaceuticals Hiring Officer Labelling Regulatory Operations
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Join Glenmark Pharmaceuticals?
- FAQs
- Summary Table
B.Pharm / M.Pharm – Officer Labelling Regulatory Operations | Mumbai
Apply now for Officer – Labelling Regulatory Operations at Glenmark Pharmaceuticals, Mumbai. Open for B.Pharm / M.Pharm with 1–3 years of experience
Join Glenmark Pharmaceuticals as Officer – Labelling Regulatory Operations
Glenmark Pharmaceuticals, a global innovation-driven pharmaceutical company, is hiring passionate professionals for the position of Officer – Labelling Regulatory Operations within the Global Regulatory Affairs team. This opportunity is ideal for candidates eager to build a rewarding career in regulatory affairs and global compliance.
At Glenmark, you’ll contribute to developing and maintaining high-quality regulatory documentation that ensures patient safety and product compliance across multiple international markets.
Company Overview
Glenmark Pharmaceuticals is a research-led, global pharmaceutical company headquartered in Mumbai, India. With a presence in over 80 countries, Glenmark focuses on discovering, developing, and marketing innovative therapies in oncology, respiratory care, and dermatology. The company is committed to improving patient outcomes through ethical research, innovation, and sustainable healthcare solutions.
As part of its Global Regulatory Affairs division, Glenmark provides opportunities to work on end-to-end regulatory documentation and submissions for regulated markets like the EU, USA, Canada, and Australia.
Job Role & Responsibilities
As an Officer – Labelling Regulatory Operations, you will:
- Manage labelling and safety assessments for Glenmark’s global pharmaceutical products.
- Review and maintain Reference Safety Information (RSI) for global submissions.
- Author and review Labelling Core Notification Forms (LCNF), Summary of Product Characteristics (SmPC), and Patient Information Leaflets (PIL) for the EU market.
- Maintain and update trackers for labelling activities and safety updates.
- Collaborate with cross-functional teams in pharmacovigilance, regulatory affairs, and medical writing.
- Gain exposure to labelling requirements for the USA, Canada, Australia, and New Zealand.
- Work with RIMS (Regulatory Information Management Systems) and eCTD submissions for document management.
This position requires a detail-oriented professional with a strong understanding of global regulatory frameworks and documentation processes.
Eligibility / Qualifications
- Qualification: B.Pharm / M.Pharm (Pharmacy, Pharmaceutical Sciences, or related field)
- Experience: 1–3 years in Regulatory Affairs or Labelling Operations
- Preferred Skills:
- Understanding of ICH, GxP, and GCP guidelines
- Experience with global submissions and safety updates
- Familiarity with electronic Common Technical Document (eCTD) format
- Strong written and verbal communication skills
Location & Salary
- Location: Mumbai, Maharashtra, India
- Work Mode: On-site, Full-time
- Compensation: Competitive salary package commensurate with experience and industry standards
Application Process
Interested and eligible candidates can apply by sending their updated resume to:
📧 purna.ambekar@glenmarkpharma.com
Apply early to secure your spot in this competitive recruitment drive at one of India’s top pharmaceutical companies.
Why Join Glenmark Pharmaceuticals?
- Opportunity to work on global regulatory submissions and labelling operations.
- Exposure to international markets and regulatory compliance standards.
- Collaborative environment fostering continuous learning and professional growth.
- Strong focus on innovation, ethics, and patient safety.
FAQs
1. What qualifications are required for this role?
Candidates should hold a B.Pharm or M.Pharm degree with relevant experience in regulatory affairs or labelling operations.
2. Is prior experience necessary?
Yes, applicants should have 1–3 years of hands-on experience in regulatory affairs, preferably with exposure to global submissions.
3. What is the work mode and location?
This is a full-time, on-site position based in Mumbai, Maharashtra.
4. How do I apply for the position?
Send your updated resume to purna.ambekar@glenmarkpharma.com and mention the position title in the subject line.
5. What is the salary range for this role?
Salary will be based on experience and aligned with Glenmark’s competitive compensation structure.
Summary Table
| Category | Details |
|---|---|
| Company | Glenmark Pharmaceuticals |
| Vacancies | Officer – Labelling Regulatory Operations |
| Required Education | B.Pharm / M.Pharm (Pharmacy, Pharmaceutical Sciences, or related fields) |
| Experience | 1–3 Years in Regulatory Affairs / Labelling Operations |
To apply for this job email your details to purna.ambekar@glenmarkpharma.com
