DRA Officer Job: The pharmaceutical industry continues to grow rapidly, and one of the most critical domains within it is Drug Regulatory Affairs (DRA). If you are a pharmacy graduate looking to build a strong career in regulatory functions, this opportunity from Brawn Laboratories could be an excellent starting point.
The company is currently hiring for the position of DRA Officer, inviting applications from freshers as well as candidates with up to 3 years of experience. This role offers hands-on exposure to regulatory documentation, dossier preparation, and compliance processes—skills that are highly valued across the global pharmaceutical sector.
DRA Officer Job Overview
- Job Title: DRA Officer
- Company: Brawn Laboratories
- Experience Required: 0 – 3 Years
- Salary Range: ₹2.25 – 3 LPA
- Job Location: Faridabad
- Industry: Pharmaceutical & Life Sciences
- Employment Type: Full-Time, Permanent
- Department: Healthcare & Life Sciences
This role is ideal for candidates who want to work closely with regulatory authorities and gain in-depth knowledge of global submission standards.
Key DRA Officer Job Highlights
Working as a DRA Officer involves contributing directly to the regulatory approval process of pharmaceutical products. The selected candidate will:
- Gain practical experience in regulatory dossier preparation and submission
- Work extensively with CTD, ACTD, and eCTD formats, which are internationally accepted documentation standards
- Handle queries raised by regulatory authorities and ensure timely responses
- Collaborate with multiple departments to gather and verify required documentation
- Ensure that all submissions comply with applicable regulatory guidelines
This is not just a job—it is a gateway into one of the most strategic and high-responsibility areas of the pharma industry.
Detailed Job Description
As a DRA Officer at Brawn Laboratories, your responsibilities will revolve around maintaining regulatory compliance and supporting product approvals.
Your core responsibilities will include:
- Regulatory Dossier Preparation & Submission: You will be responsible for compiling, reviewing, and submitting regulatory dossiers in the required formats. This includes ensuring that all scientific, technical, and legal documents are complete and accurate.
- Handling Regulatory Queries: Regulatory authorities often raise queries during the approval process. You will need to analyze these queries, coordinate with internal teams, and prepare appropriate responses within deadlines.
- Knowledge of CTD / ACTD / eCTD Formats: A strong understanding of Common Technical Document (CTD), ASEAN CTD (ACTD), and electronic CTD (eCTD) formats is essential. These formats are used globally for drug registration and approval.
- Cross-Functional Coordination: You will work closely with departments such as Quality Assurance (QA), Research & Development (R&D), and Manufacturing to collect necessary data and documentation.
- Ensuring Regulatory Compliance: Maintaining compliance with national and international regulatory guidelines is a key responsibility. Any deviation can delay approvals or lead to rejection, making accuracy extremely important.
Educational Qualification
To be eligible for this role, candidates must have:
- Undergraduate Degree: B.Pharm (any specialization)
- Postgraduate Degree: M.Pharm (preferred but not mandatory)
Fresh graduates with a strong understanding of regulatory concepts are encouraged to apply.
Required Skills
To succeed in this role, candidates should possess a combination of technical knowledge and soft skills:
- Strong understanding of Regulatory Affairs and Drug Regulatory processes
- Expertise in Dossier Preparation
- Familiarity with CTD, ACTD, and eCTD formats
- Excellent documentation and organizational skills
- Ability to coordinate effectively with multiple teams
- Good analytical and problem-solving abilities
Candidates who have completed internships or training in regulatory affairs will have an added advantage.
Career Growth in Regulatory Affairs
Drug Regulatory Affairs is one of the most promising career paths in the pharmaceutical industry. Starting as a DRA Officer can open doors to advanced roles such as:
- Regulatory Affairs Executive
- Senior Regulatory Specialist
- Global Regulatory Manager
- Dossier Strategy Expert
With experience, professionals can also work on international submissions for regulatory bodies like the USFDA, EMA, and WHO.
Working with a reputed company like Brawn Laboratories provides a solid foundation and significantly enhances your career prospects.
Location Advantage – Faridabad
The job is based in Faridabad, which is part of the National Capital Region (NCR) and a well-established industrial hub.
Advantages of working in this location include:
- Presence of multiple pharmaceutical and healthcare companies
- Better career opportunities and professional networking
- Easy connectivity to Delhi and nearby cities
Why You Should Apply
This opportunity is particularly valuable because:
- It is open to freshers, making it beginner-friendly
- It offers hands-on industry experience in regulatory affairs
- It builds a strong foundation for a long-term pharma career
- It provides exposure to global documentation standards
If you are serious about entering the regulatory domain, this role can be a turning point in your career.
Final Note
If you are a pharmacy graduate aiming to establish yourself in Drug Regulatory Affairs, this is a great opportunity to start your journey. Make sure to prepare your resume carefully and highlight any relevant training, internships, or academic projects related to regulatory work.
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