Base Medico Hiring Quality Control Officers and Senior Officers | B.Sc, M.Sc, B.Pharm Candidates Can Apply (Base Medico Hiring Quality Control Officers & Senior Officers) The pharmaceutical manufacturing industry continues to generate excellent employment opportunities for professionals specializing in Quality Control, laboratory operations, analytical testing, and regulatory compliance. Companies are increasingly seeking qualified candidates who can ensure pharmaceutical products consistently meet quality standards and regulatory requirements. BASE MEDICO PRIVATE LIMITED has announced an exciting recruitment opportunity for Quality Control professionals at its OSD manufacturing facility located in Vadodara, Gujarat. The company is looking for candidates with educational qualifications in B.Sc, M.Sc, or B. Pharm who possess strong analytical skills and practical exposure to pharmaceutical quality control systems. This opportunity is suitable for professionals seeking career growth ...
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Florencia Healthcare Hiring Regulatory Affairs Executive 2026 | B.Pharm Jobs in Noida
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Florencia Healthcare Hiring Regulatory Affairs Executive 2026 | B.Pharm Jobs in Noida
If you are planning to build a career in pharmaceutical regulatory affairs, this opportunity can be a strong starting point. The demand for regulatory professionals is increasing in 2026 as pharmaceutical companies focus more on compliance, documentation, and global submissions.
Florencia Healthcare is hiring a Regulatory Affairs Executive in Noida, offering a great opportunity for candidates who already have basic experience in dossier preparation and regulatory processes.
About The Company
Florencia Healthcare is an emerging pharmaceutical company in India, involved in the development, manufacturing, and regulatory compliance of pharmaceutical products.
The company focuses on maintaining high-quality standards and ensuring compliance with national and international regulatory guidelines. While detailed public data about the founding year and employee strength is limited, the organization is actively expanding its regulatory and product portfolio.
Working here provides exposure to drug approval processes, dossier preparation, and regulatory submissions, which are critical for a long-term career in pharma.
Job Overview Summary
The Regulatory Affairs Executive role is designed for candidates who want to specialize in pharmaceutical documentation, CTD/ACTD dossier preparation, and regulatory submissions.
This role involves working closely with different departments to compile documents, ensure compliance, and support product approvals in various markets.
Vacancy Details (Official)
Company: Florencia Healthcare
Role: Regulatory Affairs Executive
Location: Noida, Uttar Pradesh
Job Type: Full-Time
Experience: Minimum 1 Year
Salary: ₹15,000 – ₹35,000 per month
Responsibility Explanation
In this role, your main responsibility will be to prepare and manage regulatory documents required for drug approvals.
You will work on compiling CTD and ACTD dossiers, which include detailed information about the product, manufacturing, quality, and safety. You will also coordinate with internal teams to collect data and ensure everything is accurate and submission-ready.
Additionally, you will review formulations, ensure compliance with regulatory guidelines, and support the company in submitting documents to regulatory authorities.
Eligibility (Official)
B.Pharm / M.Pharm
Minimum 1 year of experience in Regulatory Affairs
Knowledge of CTD/ACTD dossier preparation
Understanding of pharmaceutical regulatory frameworks
Skills Required
To succeed in this role, you need strong attention to detail and a structured working approach.
You should be comfortable working with documentation and regulatory guidelines. Good communication skills are important because you will coordinate with multiple departments.
Basic knowledge of global regulatory processes and the ability to manage timelines will help you grow faster in this field.
Salary Estimate
The salary for this role ranges from ₹15,000 to ₹35,000 per month, depending on experience and skills.
For candidates entering regulatory affairs, this is a good starting salary, and with experience, salaries can grow significantly in this domain.
Q1. Is this job suitable for freshers? No, at least 1 year of regulatory affairs experience is required.
Q2. What is CTD in pharma? CTD (Common Technical Document) is a format used for submitting regulatory applications for drug approval.
Q3. Can B.Pharm students apply? Yes, B.Pharm and M.Pharm candidates are eligible.
Q4. What is the growth in regulatory affairs? Regulatory affairs offers strong long-term career growth with high salary potential.
Q5. Is this a good career option in 2026? Yes, regulatory affairs is one of the most stable and in-demand pharma careers.
Final Conclusion
The Regulatory Affairs Executive role at Florencia Healthcare is a valuable opportunity for candidates who want to build expertise in drug approvals, dossier preparation, and compliance.
With increasing global regulations in pharma, this field offers job stability, career growth, and international opportunities. If you already have basic experience in regulatory affairs, this role can help you take the next step in your career.
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