Are you an experienced Regulatory Affairs Coordinator looking for exciting pharmaceutical regulatory affairs jobs in Hyderabad? AET Laboratories Pvt. Ltd., a leading player in the pharma sector, is urgently hiring Sr. Executive / Executive – Regulatory Affairs for ROW markets. With 4-6 years of experience and M-Pharmacy qualification, this is your opportunity to handle CTD/ACTD submissions independently and drive compliance in dynamic regions like GCC, MENA, ASEAN, and CIS. Join a collaborative team at Gaddapotharam, Kazipally Industrial Area, and advance your career in regulatory affairs executive jobs in Hyderabad. Passionate professionals with strong regulatory expertise are encouraged to apply today!
Key Responsibilities
As a Regulatory Affairs Coordinator at AET Laboratories, you will play a pivotal role in ensuring seamless regulatory compliance for international markets. Your day-to-day duties will include:
- Independently managing CTD and ACTD country-specific submissions for ROW markets, including GCC, MENA, ASEAN, and CIS regions.
- Overseeing product lifecycle activities to ensure timely updates and full compliance with evolving regulations.
- Maintaining up-to-date knowledge of current regulatory guidelines and enforcing adherence across all processes.
- Collaborating closely with the Business Development team and clients to develop effective regulatory strategies and deliver high-quality submissions.
- Demonstrating strong communication and interpersonal skills to facilitate cross-functional coordination.
These responsibilities make this one of the most sought-after regulatory affairs jobs in Hyderabad for experienced professionals focusing on ROW markets.
Qualifications and Requirements
To excel in this Sr. Executive Regulatory Affairs job in Hyderabad, candidates must meet the following criteria:
- Experience: 4-6 years in regulatory affairs, specifically in pharmaceutical submissions for international markets.
- Education: M-Pharmacy (Master of Pharmacy) is mandatory.
- Designation Level: Executive or Sr. Executive.
- Skills: Expertise in CTD/ACTD dossiers, deep understanding of ROW regulatory guidelines (GCC, MENA, ASEAN, CIS), product lifecycle management, and excellent communication abilities.
- Key Traits: Ability to work independently, stay updated on regulatory changes, and collaborate with BD teams and clients.
AET Laboratories values professionals who bring proven experience in pharmaceutical regulatory affairs coordinator roles in Hyderabad and a passion for innovation in compliance.
Benefits of Joining AET Laboratories
Working at AET Laboratories offers more than just a job—it’s a career growth opportunity in a growing, innovative company. Employees enjoy:
- Competitive salary package in a leading pharma firm.
- Exposure to diverse ROW markets, enhancing global regulatory expertise.
- Collaborative environment that values expertise, teamwork, and professional development.
- Opportunity to make significant impact on product approvals and lifecycle management.
- Stable location in Hyderabad’s thriving Kazipally Industrial Area.
This role is ideal for those searching for M-Pharmacy regulatory affairs jobs in Hyderabad with 4-6 years experience.
How to Apply
Interested candidates should send their updated resume to k.surendra@tiefenbacher.com immediately. Mention “Application for Regulatory Affairs Coordinator – ROW Markets” in the subject line.
Company Address: Survey No.: 42, Gaddapotharam, Kazipally Industrial Area, Sanga Reddy Dist., Hyderabad-502319, Telangana, India.
Don’t miss this chance to secure regulatory affairs executive vacancies in Hyderabad at AET Laboratories Pvt. Ltd.
Frequently Asked Questions (FAQs)
1. What is the experience required for Regulatory Affairs Coordinator jobs at AET Laboratories in Hyderabad?
Candidates need 4-6 years of experience in regulatory affairs, with expertise in CTD/ACTD submissions for ROW markets like GCC, MENA, ASEAN, and CIS.
2. Is M-Pharmacy mandatory for these Sr. Executive Regulatory Affairs roles in Hyderabad?
Yes, M-Pharmacy qualification is required. The positions are at Executive and Sr. Executive levels in the Regulatory Affairs-ROW department.
