Inspiron RegTech Hiring Regulatory Affairs Officer
- Company Overview
- Job Role & Responsibilities
- Regulatory Affairs Officer
- Eligibility / Qualifications
- Location & Salary Insights
- Application Process
- Why Choose a Career in Regulatory Affairs?
- Career Outlook in Regulatory Compliance
- Frequently Asked Questions (FAQs)
- 1. Are freshers eligible for this role?
- 2. Is prior regulatory experience mandatory?
- 3. What computer skills are required?
- 4. Which qualifications are accepted?
- 5. How can I apply?
- Job Summary
BPharm MPharm RA Officer Vacancy at Inspiron
BPharm, MPharm, MSc Regulatory Affairs Officer vacancy for freshers/experienced at Inspiron RegTech. Apply via email.
Inspiron RegTech is hiring for the position of Regulatory Affairs Officer, inviting applications from pharmacy and analytical chemistry graduates who are looking to build or advance their careers in pharmaceutical regulatory affairs. Both freshers and experienced candidates are eligible to apply, making this a strong opportunity for individuals seeking entry into the highly specialized and high-growth regulatory compliance domain.
Regulatory Affairs is one of the most critical and high-value segments within the pharmaceutical and life sciences industry. As global regulatory standards become stricter, demand for skilled regulatory professionals continues to rise. If you have a background in B.Pharm, M.Pharm, or M.Sc Analytical Chemistry and want to work in pharmaceutical documentation, drug approval processes, and compliance management, this role offers a structured pathway.
Company Overview
Inspiron RegTech operates in the pharmaceutical regulatory and compliance support space. Companies in the regulatory consulting and compliance management sector play a key role in helping pharmaceutical manufacturers meet domestic and international approval requirements.
Regulatory Affairs professionals ensure that pharmaceutical products comply with national and international guidelines before reaching patients. This includes documentation preparation, dossier compilation, submission tracking, and coordination with regulatory authorities.
Working in a regulatory-focused organization provides exposure to:
- Drug regulatory documentation processes
- Dossier preparation (CTD/eCTD formats)
- Pharmaceutical compliance standards
- Product registration procedures
- International regulatory frameworks
As pharmaceutical exports and global drug registrations increase, regulatory affairs careers continue to gain strategic importance within the life sciences ecosystem.
Job Role & Responsibilities
Regulatory Affairs Officer
Qualification: M.Sc (Analytical Chemistry), M.Pharm (QA, Regulatory Affairs, Pharmaceutics), B.Pharm
Experience: Freshers / Experienced Candidates
Skill Requirement: Basic computer knowledge (Excel, Word, Email communication)
Key Responsibilities:
- Assisting in preparation and review of regulatory documents
- Supporting compilation of CTD and eCTD dossiers
- Coordinating with internal departments for documentation collection
- Maintaining regulatory submission records
- Reviewing technical data for compliance alignment
- Supporting variation filings and post-approval changes
- Ensuring documentation accuracy and data integrity
Freshers selected for this role will gain foundational exposure to pharmaceutical regulatory systems, while experienced candidates may handle more independent submission responsibilities.
Strong attention to detail and documentation discipline are essential for success in this role.
Eligibility / Qualifications
Educational Qualifications (comma-separated):
M.Sc Analytical Chemistry, M.Pharm Quality Assurance, M.Pharm Regulatory Affairs, M.Pharm Pharmaceutics, B.Pharm
Eligibility Criteria:
- Freshers with strong academic background can apply
- Experienced candidates with regulatory documentation exposure preferred
- Basic knowledge of Microsoft Excel, Word, and email communication required
- Strong written communication skills
- Understanding of pharmaceutical manufacturing and quality systems preferred
Regulatory Affairs roles demand precision, compliance awareness, and structured documentation practices. Candidates lacking documentation discipline may struggle in this domain.
Location & Salary Insights
The job location is associated with Inspiron RegTech operations (specific location details will be shared during the recruitment process).
Salary will depend on:
- Educational qualification
- Regulatory documentation exposure
- Communication skills
- Industry experience (if any)
Regulatory Affairs is considered a high-growth pharmaceutical career path due to increasing global compliance requirements, USFDA guidelines, WHO-GMP frameworks, and international drug approval systems.
Professionals in this field often progress into:
- Regulatory Affairs Executive
- Senior Regulatory Affairs Associate
- Dossier Specialist
- Regulatory Compliance Manager
- Global Regulatory Affairs Manager
With experience, regulatory professionals command strong compensation due to the technical complexity and compliance risk associated with pharmaceutical approvals.
Application Process
Interested candidates should send their updated CV to:
Email: hr@inspironregtech.com
Application Steps:
- Update your CV highlighting regulatory, QA, or pharmaceutical academic projects.
- Mention any exposure to dossier preparation or documentation systems.
- Ensure computer proficiency is clearly stated.
- Send your application via email.
Shortlisted candidates will be contacted for further evaluation.
Why Choose a Career in Regulatory Affairs?
Pharmaceutical Regulatory Affairs professionals act as the bridge between drug development and market approval. Without regulatory clearance, pharmaceutical products cannot reach patients.
This field offers:
- Stable career growth
- High compliance-driven demand
- Opportunities in global markets
- Exposure to international regulatory standards
- Long-term leadership pathways in compliance management
As pharmaceutical exports expand globally, regulatory expertise becomes increasingly valuable. Early entry into this domain provides a strong long-term advantage.
Career Outlook in Regulatory Compliance
India’s pharmaceutical industry is among the largest globally. Increasing exports to regulated markets such as the US and Europe require strict documentation and submission processes.
Professionals trained in:
- CTD/eCTD submissions
- Regulatory documentation review
- Compliance management systems
- Post-approval variations
- Audit documentation support
are positioned for consistent career advancement.
Regulatory Affairs is less saturated compared to production roles, making it a strategic choice for pharmacy graduates.
Frequently Asked Questions (FAQs)
1. Are freshers eligible for this role?
Yes. Freshers with relevant pharmacy or analytical chemistry qualifications can apply.
2. Is prior regulatory experience mandatory?
No. Experienced candidates are preferred but freshers are eligible.
3. What computer skills are required?
Basic knowledge of MS Excel, Word, and email communication is mandatory.
4. Which qualifications are accepted?
M.Sc Analytical Chemistry, M.Pharm (QA/RA/Pharmaceutics), and B.Pharm.
5. How can I apply?
Send your CV to hr@inspironregtech.com.
Job Summary
| Company | Inspiron RegTech |
|---|---|
| Vacancies | Regulatory Affairs Officer |
| Required Education | M.Sc Analytical Chemistry, M.Pharm (QA/RA/Pharmaceutics), B.Pharm |
| Experience | Freshers / Experienced |
To apply for this job email your details to hr@inspironregtech.com
