Freshers Hiring for Regulatory Affairs and Project Management at RegTech India
Location: Ahmedabad, Gujarat
Job Roles: Regulatory Affairs Officers & Project Management Officers
Experience Required: 0–1 Year
Qualification: B.Pharm, M.Pharm, M.Sc
RegTech India, a rising leader in regulatory compliance and pharmaceutical project management, has opened multiple fresh job opportunities for aspiring candidates in the pharmaceutical and life sciences fields. This is an excellent chance for freshers to begin their career journey in one of India’s most promising pharma-tech organizations. Freshers Hiring for Regulatory Affairs and Project Management
This recruitment drive by RegTech India is aimed at expanding its dedicated team for Regulatory Affairs and Project Management. The company is looking for enthusiastic, detail-oriented, and ambitious professionals who are ready to work on high-impact pharmaceutical regulatory and GMP projects.
About RegTech India
RegTech India Solutions is headquartered in Ahmedabad, Gujarat, and is recognized for its cutting-edge solutions in regulatory affairs, pharmacovigilance, clinical research, and Good Manufacturing Practices (GMP). The company assists pharmaceutical and biotechnology clients in converting complex compliance requirements into streamlined business operations. Freshers Hiring for Regulatory Affairs and Project Management
It also manages PharmaBharat.com, a fast-growing digital platform for pharmaceutical professionals. The platform delivers the latest industry updates, job opportunities, and expert insights for candidates across India.
Current Openings at RegTech India
RegTech India is hiring for the following roles with 0–1 year of experience. These positions are full-time, and preference will be given to candidates located in or around Ahmedabad, Gujarat. Freshers Hiring for Regulatory Affairs and Project Management
1. Project Management Officer
Qualification: B.Pharm
Experience: 0–1 year
Location: Ahmedabad
Key Responsibilities:
- Coordinate project activities across departments like Regulatory Affairs, Pharmacovigilance, Clinical, and GMP.
- Maintain trackers, submission logs, and other regulatory documentation.
- Collaborate with internal teams and external clients to ensure timely project delivery.
- Track milestones and ensure compliance with regulatory deadlines.
This role is ideal for pharmacy graduates who are organized, proactive, and keen on building careers in pharmaceutical project coordination. Freshers Hiring for Regulatory Affairs and Project Management
2. Regulatory Affairs Officer – Clinical Focus
Qualification: M.Pharm (Clinical Pharmacy)
Experience: 0–1 year
Location: Ahmedabad
Key Responsibilities:
- Support clinical regulatory submissions using sound knowledge of clinical pharmacy.
- Draft, compile, and review regulatory documents as per CTD/ACTD formats (Modules 1–5).
- Work extensively with MS Word and Excel for documentation tasks.
- Ensure regulatory submissions meet accuracy and quality standards.
This position is perfect for fresh clinical pharmacy postgraduates who want to step into the regulatory world and contribute to clinical documentation and submissions. Freshers Hiring for Regulatory Affairs and Project Management
3. Regulatory Affairs Officer – QA & Analytical Chemistry
Qualification: M.Pharm (Quality Assurance) or M.Sc (Analytical Chemistry)
Experience: 0–1 year
Location: Ahmedabad
Key Responsibilities:
- Prepare high-quality documents for quality assurance and analytical chemistry-related submissions.
- Work with ICH guidelines and ensure accurate CTD dossier structuring.
- Use Excel, Word, and regulatory software tools to manage compliance documentation.
- Collaborate with cross-functional teams for successful dossier preparation and audit readiness.
This role suits candidates with a strong grasp of regulatory principles, attention to detail, and proficiency in documentation tools. Freshers Hiring for Regulatory Affairs and Project Management
Why Join RegTech India?
Choosing RegTech India as your first employer can provide a strong foundation for a long-term career in the pharmaceutical industry. Here’s what makes RegTech a desirable workplace for freshers:
- Exposure to Live Projects: Work directly on regulatory submissions, clinical documentation, and GMP audits.
- Mentorship & Learning: Learn from senior professionals and regulatory experts who guide you through real-world challenges.
- Skill Development: Gain hands-on experience in global regulatory standards, documentation tools, and client communication.
- Collaborative Work Culture: Join a team that values cooperation, learning, and professional growth.
- Career Advancement: Opportunity to grow within the organization based on performance, initiative, and learning aptitude.
How to Apply for RegTech India Jobs?
Eligible and interested candidates can apply by sending their latest resume or CV to the official HR email address:
📧 hr.regtechindia@gmail.com
When applying, mention the Job Title in the subject line of your email. Candidates who are local to Ahmedabad or willing to relocate will be given preference.
Important Tips Before You Apply
- Ensure that your resume highlights your educational qualifications, internships (if any), and software skills (especially MS Word and Excel).
- Customize your cover letter to explain why you are interested in Regulatory Affairs or Project Management.
- Showcase any project work or thesis related to pharmaceutical documentation, quality assurance, or clinical trials.
- Freshers Hiring for Regulatory Affairs and Project Management
Final Thoughts
If you are a B.Pharm, M.Pharm, or M.Sc graduate with 0–1 year of experience and are looking to break into the pharmaceutical regulatory or project management domain, RegTech India’s hiring drive is a great opportunity. With a dynamic work culture and exposure to live global projects, this is the right time to begin your professional journey. Freshers Hiring for Regulatory Affairs and Project Management
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