Yash Pharma Laboratories Pvt. Ltd. is hiring for the positions of Regulatory Affairs Executive / Senior Executive at its Thane, Maharashtra location. Candidates with 1–3 years of hands-on experience in pharmaceutical regulatory affairs and a Bachelor’s or Master’s degree in Pharmacy or Life Sciences can apply.
The role involves preparing and reviewing regulatory dossiers, coordinating with cross-functional teams, supporting submissions to regulatory authorities, maintaining regulatory documentation, and reviewing product artwork for compliance.
About Yash Pharma Laboratories Pvt. Ltd.
Established in 1972, Yash Pharma Laboratories Pvt. Ltd. focuses on pharmaceutical solutions, scientific advancement, and portfolio innovation, guided by its purpose of “Healing the World with Compassion.”
The company’s focus areas include dermatology, patient health, quality care, and collaboration with healthcare professionals and stakeholders. Its global export operations involve teams working across business development, regulatory affairs, product management, and logistics to support the delivery of finished pharmaceutical formulations to international markets.
Yash Pharma Laboratories also provides contract-manufacturing services to pharmaceutical companies in India. Its manufacturing portfolio includes external preparations, liquids, tablets, and nasal sprays.
The company also states that it is USFDA-approved for external preparations.
For more information, visit the official website: https://yashpharma.com/
Regulatory Affairs Executive / Senior Executive Vacancy Details
Yash Pharma Laboratories is looking for a Regulatory Affairs professional to join its Regulatory team in Thane, Maharashtra.
The position is suited to candidates with practical experience in pharmaceutical regulatory affairs, particularly those familiar with regulatory documentation, dossier preparation, and submission requirements for domestic and international markets.
Experience required: 1–3 years in pharmaceutical regulatory affairs.
Job location: Thane, Maharashtra, India.
Eligibility Criteria and Qualifications
Candidates interested in this opportunity should meet the following requirements:
- Educational qualification: Bachelor’s or Master’s degree in Pharmacy or Life Sciences.
- Professional experience: 1–3 years of experience in pharmaceutical regulatory affairs.
- Regulatory knowledge: Understanding of regulatory submissions and country-specific requirements.
- Communication skills: Strong communication and coordination abilities.
- Organizational skills: Ability to manage regulatory documentation and related activities systematically.
Candidates with relevant pharmaceutical regulatory affairs experience and the required educational background can consider applying.
Key Responsibilities of the Regulatory Affairs Executive
The role involves supporting regulatory documentation, submissions, and compliance-related activities, including:
- Preparing, compiling, and reviewing regulatory dossiers in CTD and ACTD formats for submission to regulatory authorities.
- Supporting regulatory submissions for ROW (Rest of World), MENA, LATAM, EU, and UK markets.
- Coordinating with Quality Assurance (QA), Quality Control (QC), Research and Development (R&D), and Production teams to obtain the documents required for regulatory submissions.
- Liaising with national and international regulatory agencies to support timely submissions and approvals.
- Keeping up to date with applicable regulatory guidelines, including those associated with WHO and USFDA, and supporting compliance-related activities.
- Maintaining and updating regulatory databases, submission trackers, and documentation systems.
- Reviewing product artwork, labels, and promotional materials for regulatory compliance.
This position combines dossier preparation, regulatory coordination, document management, and review of product-related materials across pharmaceutical markets.
Skills Required for This Regulatory Affairs Job
Candidates should have a sound understanding of pharmaceutical regulatory guidelines and documentation processes for domestic and international markets.
Relevant knowledge of CTD/ACTD dossier preparation, country-specific submission requirements, and regulatory documentation is important for the advertised role.
The position also calls for strong communication, coordination, and organizational skills. The ability to work with cross-functional departments and maintain systematic regulatory records is relevant to the responsibilities involved.
How to Apply for the Yash Pharma Regulatory Affairs Vacancy
Interested candidates can apply by sending their updated resume to the following email address:
Application email: regulatory2@yashpharma.com
Before applying, ensure that your resume clearly presents your educational qualifications, pharmaceutical regulatory affairs experience, and relevant dossier preparation or submission work.
Use the application contact details carefully, and avoid paying recruitment fees to individuals or intermediaries without independently establishing the legitimacy of the request.
Frequently Asked Questions
1. What qualification is required for the Yash Pharma Regulatory Affairs vacancy?
Candidates should have a Bachelor’s or Master’s degree in Pharmacy or Life Sciences.
2. How much experience is required for this position?
The stated requirement is 1–3 years of experience in pharmaceutical regulatory affairs.
3. Where is the Regulatory Affairs Executive job located?
The position is located in Thane, Maharashtra, India.
4. How can candidates apply for this vacancy?
Candidates can send their updated resume to regulatory2@yashpharma.com.