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Regulatory Affairs Executive Opening at VINS Bioproducts Limited
The pharmaceutical and life sciences industry continues to expand rapidly, creating exciting career opportunities for regulatory professionals. If you are an experienced Regulatory Affairs Executive with expertise in sterile injectable products, this opportunity in Hyderabad could be the next step in your career. VINS Bioproducts Limited is looking for a skilled professional who can manage regulatory submissions, documentation, and compliance activities in the pharmaceutical sector. This Life Sciences Job offers excellent exposure to regulatory processes and an opportunity for Immediate Joining for qualified candidates.
About VINS Bioproducts Limited
VINS Bioproducts Limited is a leading biopharmaceutical company specializing in the development and manufacturing of life-saving biological products. The company focuses on producing high-quality antivenoms, vaccines, and injectable pharmaceutical products that meet international regulatory standards. With advanced manufacturing facilities and strong R&D capabilities, VINS Bioproducts plays a crucial role in delivering innovative healthcare solutions globally while maintaining strict compliance with pharmaceutical regulatory guidelines.
Job Description:
- Job Title: Regulatory Affairs Executive – Injectable (Pharmaceutical)
- Company: VINS Bioproducts Limited
- Location: Hyderabad
- Role: Regulatory Affairs Executive
- Experience: 2–5 Years
- Salary: Depends on Previous CTC
- Joining: Immediate Joiner Preferred
Job Summary
We are looking for a Regulatory Affairs Executive with experience in the pharmaceutical domain, specifically sterile injectable products. The candidate will be responsible for handling regulatory submissions, documentation, and compliance activities related to injectable formulations.
Key Responsibilities
- Preparation, compilation, and submission of regulatory dossiers for injectable pharmaceutical products.
- Handling CTD/eCTD documentation and maintaining regulatory records.
- Preparation and submission of applications to Central Drugs Standard Control Organization (CDSCO) and other regulatory authorities.
- Coordination with internal departments such as Quality Assurance, Manufacturing, and R&D for regulatory documentation.
- Reviewing regulatory guidelines and ensuring compliance with current regulatory requirements.
- Preparation and review of product registration documents, variations, amendments, and renewals.
- Maintaining regulatory database and ensuring timely submissions.
- Supporting regulatory inspections and audits when required.
Required Qualifications
- Master’s/Bachelor’s degree in Pharmacy, Biotechnology, Life Sciences, or related field.
- 2–5 years of experience in Regulatory Affairs within the pharmaceutical industry.
- Mandatory experience in sterile injectable products.
- Strong knowledge of pharmaceutical regulatory guidelines and documentation.
- Good communication and coordination skills.
Preferred Candidate
- Immediate joiners will be given preference.
- Experience handling injectable regulatory submissions is highly desirable.
APPLY ONLINE HERE
