Join KAMLA Lifesciences Ltd. as a Regulatory Affairs Officer for injectable products. This pharma job offers excellent opportunities in global regulatory submissions with 2-6 years of experience required. Ideal for professionals seeking pharmaceutical careers in India.
Contents
- 1 About the Company
- 2 Job Details
- 3 Job Description
- 4 Skills/Qualifications
- 5 Key Responsibilities
- 6 Benefits/Perks
- 7 How to Apply
- 8 Why You Should Join
- 9 FAQs
- 9.1 Q1. What is the required experience for the Regulatory Affairs Officer position?
- 9.2 Q2. Is this position suitable for freshers?
- 9.3 Q3. Which markets will I handle in this job?
- 9.4 Q4. How can I apply for this pharma job in Boisar, Tarapur?
- 9.5 Q5. What growth opportunities does KAMLA Lifesciences offer?
About the Company
KAMLA Lifesciences Ltd. is a fast-growing injectable manufacturing company committed to delivering quality medicines that improve lives. With a strong focus on innovation, regulatory compliance, and global standards, the company specializes in high-quality injectables for various international markets including the US, EU, and ROW regions.
Known for its collaborative culture and patient-centric approach, KAMLA Lifesciences provides a supportive environment where professionals can grow while contributing to better health outcomes worldwide.
Job Details
- Company Name: KAMLA Lifesciences Ltd.
- Experience: 2-6 Years (Injectable background mandatory)
- Qualification: B.Pharm / M.Pharm in Life Sciences
- Location: Boisar, Tarapur
- Work Type: On-site
Job Description
KAMLA Lifesciences Ltd. is hiring a talented Regulatory Affairs Officer to strengthen its Regulatory Affairs team. This role is critical for ensuring timely submissions and compliance across global markets for injectable products. The position offers significant exposure to international regulatory frameworks and lifecycle management.
- Regulatory Affairs Officer Department: Regulatory Affairs
- Market: USFDA, EU, TGA, ROW
- Role: Regulatory Affairs Officer (Injectables)
- Experience: 2-6 Years
- Education/Qualification: B.Pharm / M.Pharm in Life Sciences
Skills/Qualifications
- Strong injectable background with hands-on regulatory experience
- Exposure to USFDA, EU, TGA, or other international regulatory submissions
- Excellent knowledge of eCTD/CTD dossier preparation and submissions
- Proficiency in handling product registrations, variations, and renewals
- Strong communication, analytical, and documentation skills
- Ability to coordinate effectively with cross-functional teams
- Thorough understanding of global regulatory guidelines and local regulations
Key Responsibilities
- Preparation, review, and submission of regulatory documents (CTD/eCTD)
- Handling product registrations, variations, renewals, and lifecycle management
- Responding to regulatory queries and deficiency letters
- Ensuring compliance with global regulatory guidelines
- Coordinating with cross-functional teams for timely submissions
Benefits/Perks
- Work on challenging global regulatory submissions across diverse markets
- Collaborative, supportive, and growth-oriented work culture
- Excellent opportunities to learn, develop skills, and make a meaningful impact
- Be part of a rapidly expanding injectable manufacturing company
- Long-term career growth in a compliance-focused environment
How to Apply
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the KAMLA Lifesciences Ltd. career page.
Interested candidates meeting the requirements can send their updated CV to anjali.yadav@kamlagroup.co.in.
For more information, contact: 8956480712 / 7972964497.
Don’t miss this excellent pharma job opportunity in Regulatory Affairs. Apply now and take the next step in your pharmaceutical career.
For more regulatory affairs jobs, QA jobs, QC jobs, and production jobs across India, visit Pharma Recruiter.
Why You Should Join
KAMLA Lifesciences Ltd. offers a dynamic workplace where compliance meets innovation. Employees benefit from a supportive culture that values professional growth and recognizes contributions to quality healthcare.
With expertise in injectables and a commitment to global standards, joining the team means long-term career stability, continuous learning, and the chance to work on impactful projects that reach patients worldwide. The company’s focus on “Quality Today, Compliance Always, Better Health Tomorrow” creates an inspiring environment for regulatory professionals.
FAQs
Q1. What is the required experience for the Regulatory Affairs Officer position?
A: Candidates need 2-6 years of experience in Regulatory Affairs with a mandatory injectable background.
Q2. Is this position suitable for freshers?
A: No, this role requires relevant industry experience in regulatory affairs, particularly with injectables.
Q3. Which markets will I handle in this job?
A: The role involves submissions for USFDA, EU, TGA, ROW, and other international markets.
Q4. How can I apply for this pharma job in Boisar, Tarapur?
A: Mail your CV to anjali.yadav@kamlagroup.co.in or call 8956480712 / 7972964497 for details.
Q5. What growth opportunities does KAMLA Lifesciences offer?
A: The company provides global exposure, skill development, and career advancement in a growing injectable manufacturing setup.
