JAMP India Hiring Officer/Sr. Officer – Regulatory Affairs
JAMP India Pharmaceuticals hiring Officer/Sr. Officer in Regulatory Affairs (Biosimilars). Apply now for exciting pharma career opportunities.
JAMP India Pharmaceuticals, a fast-growing player in the global pharmaceutical industry, is expanding its Regulatory Affairs (Biosimilars) team. The company is inviting applications for Officer and Senior Officer positions. This is an excellent opportunity for skilled pharma professionals seeking to build a rewarding career in biosimilars regulatory affairs while contributing to compliance and healthcare innovation.
Company Overview
JAMP India Pharmaceuticals is recognized for its commitment to high-quality medicines and regulatory excellence, with a strong footprint in the biosimilars and generics market. With a collaborative work environment and focus on compliance with international standards, JAMP India continues to strengthen its presence in regulated markets, including Canada, the US, and Europe.
Job Role & Responsibilities
As an Officer / Senior Officer in Regulatory Affairs (Biosimilars), you will:
- Assist in preparing post-approval submissions such as Notifiable Changes, Supplemental New Drug Submissions, and New Drug Submissions under supervision
- Support preparation of response packages for Health Canada queries, ensuring timely delivery to avoid review delays
- Ensure documentation is scientifically accurate, complete, and in compliance with applicable guidelines
- Collaborate with cross-functional teams to ensure smooth regulatory submission processes
- Gain exposure to international regulatory frameworks and biosimilar product development compliance
Eligibility / Qualifications
- Qualification: B.Pharm, M.Pharm, M.Sc (Regulatory Affairs, Life Sciences, Pharmaceutical Sciences)
- Experience: 2–6 years (Regulatory Affairs experience preferred; biosimilars experience a plus)
- Key Skills:
- Knowledge of regulatory submission processes
- Familiarity with Health Canada guidelines
- Strong technical writing and documentation skills
Relevant education backgrounds include: B.Pharm, M.Pharm (Regulatory Affairs, Pharmaceutical Technology, Quality Assurance), M.Sc (Life Sciences, Biotechnology, Microbiology, Biochemistry).
Location & Salary
- Work Location: JAMP India Pharmaceuticals (specific location details available upon application)
- Salary: Competitive package based on experience and role
- Type: Full-time permanent role
Application Process
Interested candidates may apply directly by sending their updated CV to the company’s HR team (official email will be shared upon application request).
Apply soon to secure your opportunity with JAMP India Pharmaceuticals.
Why Join JAMP India?
- Exposure to global regulatory markets including Canada, US, and Europe
- Hands-on experience in biosimilars regulatory submissions
- Career growth in a fast-expanding pharmaceutical company
- Collaborative work environment with expert mentors
FAQs
Q1: What is the qualification required?
B.Pharm, M.Pharm, or M.Sc in Regulatory Affairs, Life Sciences, or related fields.
Q2: What experience level is needed?
2–6 years of experience in Regulatory Affairs; freshers with strong academic background may be considered for Officer level.
Q3: What is the role’s focus?
Preparation of regulatory submissions for biosimilars and responses to Health Canada.
Q4: Where is the job location?
At JAMP India Pharmaceuticals; detailed location will be shared during the recruitment process.
Q5: How do I apply?
Send your CV to the HR contact provided in the official job posting.
Summary Table
| Category | Details |
|---|---|
| Company | JAMP India Pharmaceuticals |
| Vacancies | Officer / Senior Officer – Regulatory Affairs (Biosimilars) |
| Required Education | B.Pharm, M.Pharm, M.Sc (Regulatory Affairs, Life Sciences, Pharmaceutical Sciences) |
| Experience | 2–6 years (Regulatory Affairs; biosimilars experience preferred) |
