Allrite Pharma: Company Introduction
Allrite Pharma, a leading name in the pharmaceutical industry, specializes in the development, manufacturing, and regulatory compliance of high-quality medicinal products. With a strong commitment to innovation and excellence, the company caters to a global market, ensuring its products meet the stringent requirements of international regulatory authorities. Located in the thriving industrial hub of Baddi, Allrite Pharma is a preferred employer for skilled professionals looking to advance their careers in regulatory affairs.
Responsibilities in the Job
As a Regulatory Affairs professional at Allrite Pharma, you will play a crucial role in ensuring compliance with regulatory standards for the EU market. Key responsibilities include:
- Preparing, reviewing, and submitting dossiers for EU market approvals.
- Managing regulatory documentation and ensuring timely filings.
- Liaising with regulatory authorities and addressing queries effectively.
- Staying updated on EU regulatory guidelines and ensuring adherence to them.
- Supporting product lifecycle management, including amendments and renewals.
Qualifications Required
To qualify for this position, candidates must possess the following:
- A degree in M.Sc, M.Pharm, or B.Pharm.
- 2 to 6 years of experience in regulatory affairs, specifically with EU market exposure.
Skills and Expertise
- Comprehensive knowledge of EU regulatory requirements and dossier preparation.
- Strong analytical and problem-solving abilities.
- Excellent written and verbal communication skills.
- Ability to manage multiple projects and meet strict deadlines.
- Proficiency in regulatory software tools and MS Office applications.
How to Apply
Interested candidates can apply by sending their updated resume to one of the following email addresses:
- regulatory@allrite.in
