Kamla Group Hiring Regulatory Affairs Officer
- Regulatory Affairs Officer Opening | Kamla Group | Boisar, Maharashtra
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Join Kamla Group of Companies?
- High CPC Keywords Used Naturally
- FAQs
- Summary Table
Regulatory Affairs Officer Opening | Kamla Group | Boisar, Maharashtra
Kamla Group hiring Regulatory Affairs Officer for injectable formulation plant at Boisar, Maharashtra. 1–3 years experience required.
Kamla Group of Companies, a trusted name in pharmaceutical manufacturing, is looking for talented professionals to join its Injectable Formulation Plant in Boisar, Maharashtra. The company is hiring for the role of Regulatory Affairs Officer, a vital position responsible for ensuring compliance with global regulatory standards, dossier submissions, and product approvals.
Company Overview
Kamla Group of Companies is one of India’s leading pharmaceutical manufacturers, specializing in injectable formulations, oral solids, and sterile manufacturing for both domestic and international markets. The company is recognized for its commitment to quality, innovation, and patient safety, and has established regulatory approvals across USFDA, EU, WHO-GMP, and other global authorities.
With a focus on research-driven growth, Kamla Group’s facilities are equipped with modern technology and compliant infrastructure that meets stringent regulatory expectations. The organization offers its employees exposure to international pharmaceutical operations and a culture that values precision, teamwork, and professional development.
Job Role & Responsibilities
As a Regulatory Affairs Officer, you will play a critical role in supporting the company’s compliance and registration activities across regulated and semi-regulated markets.
Key Responsibilities:
- Prepare, compile, and submit regulatory dossiers for USFDA, EU, WHO, and ROW markets.
- Review and maintain technical documentation to ensure regulatory accuracy.
- Coordinate with R&D, QA, QC, and production teams for data collection and compliance support.
- Respond to regulatory queries, deficiency letters, and agency communications.
- Monitor global regulatory updates and maintain product lifecycle management documentation.
- Ensure timely submission and approval of product applications.
Eligibility / Qualifications
Education:
B.Pharm, M.Pharm, or M.Sc in Pharmaceutical Sciences, Chemistry, or related life sciences disciplines.
Experience:
1–3 years in Regulatory Affairs, preferably within sterile or injectable formulation manufacturing.
Preferred Skills:
- Proficiency in CTD/eCTD dossier preparation and submission.
- Familiarity with global regulatory frameworks (USFDA, EMA, WHO, TGA).
- Strong understanding of product registration procedures and post-approval documentation.
- Excellent communication and coordination skills.
- Attention to detail and ability to manage multiple projects simultaneously.
Location & Salary
Location: MIDC, Boisar, Maharashtra
Experience Required: 1–3 Years
Salary: Competitive; based on qualifications and experience.
Industry: Pharmaceutical Manufacturing (Injectable Formulation)
Application Process
Interested candidates can send their updated resumes directly to the HR department or connect through LinkedIn.
Contact Details:
- Email: Anjali.Yadav@kamlagroup.co.in
- Phone: 8956480712 / 7972964497
- LinkedIn: Kamla Lifesciences Ltd
Why Join Kamla Group of Companies?
- Opportunity to work in a globally recognized injectable formulation facility.
- Exposure to regulated market documentation and international submission processes.
- Career progression within a quality-focused, fast-growing pharmaceutical company.
- Collaborative environment promoting innovation and technical learning.
High CPC Keywords Used Naturally
pharmaceutical regulatory affairs jobs, injectable formulation vacancies, B.Pharm openings Maharashtra, M.Pharm regulatory roles, CTD dossier submission jobs, USFDA regulatory compliance, pharma documentation jobs India, WHO-GMP approved pharma companies, regulatory affairs officer careers, high-paying pharma jobs.
FAQs
1. What is the role of a Regulatory Affairs Officer?
The Regulatory Affairs Officer manages dossier preparation, compliance submissions, and communication with regulatory agencies for global product approvals.
2. Who can apply for this position?
Candidates with B.Pharm, M.Pharm, or M.Sc qualifications and 1–3 years of experience in regulatory affairs (injectables preferred).
3. Where is the work location?
The position is based at Kamla Group’s injectable formulation plant in Boisar, Maharashtra.
4. What kind of experience is preferred?
Candidates with prior exposure to CTD/eCTD dossier preparation, regulatory submissions, and sterile formulation documentation.
5. How can I apply?
Email your updated CV to Anjali.Yadav@kamlagroup.co.in or contact the HR numbers provided.
Summary Table
| Category | Details |
|---|---|
| Company | Kamla Group of Companies |
| Vacancies | Regulatory Affairs Officer (Injectable Formulation Plant) |
| Required Education | B.Pharm, M.Pharm, M.Sc (Pharmaceutical Sciences, Chemistry, Life Sciences) |
| Experience | 1–3 Years |
| Location | MIDC, Boisar, Maharashtra |
| Anjali.Yadav@kamlagroup.co.in | |
| Contact | 8956480712 / 7972964497 |

To apply for this job email your details to Anjali.Yadav@kamlagroup.co.in