Sandoz Hiring Regulatory Affairs Specialist Hyderabad – Apply Now
- About Sandoz
- Job Details: Regulatory Affairs Specialist
- Key Responsibilities
- Qualifications and Skills Required
- Commitment to Diversity and Inclusion
- How to Apply
- Frequently Asked Questions (FAQs)
Sandoz Hiring Regulatory Affairs Specialist Hyderabad: Apply Now
Sandoz, a global leader in generic and biosimilar medicines, is currently hiring for the position of Regulatory Affairs Specialist in Hyderabad, Telangana. This is an excellent opportunity for professionals with a background in life sciences and regulatory compliance to join a company that is shaping the future of affordable healthcare. If you are passionate about ensuring compliance, managing projects, and working in a collaborative environment, this role is perfect for you.
About Sandoz
Sandoz is a pioneer in the generic and biosimilar medicines sector, touching the lives of nearly 500 million patients worldwide. With a commitment to innovation, sustainability, and inclusivity, Sandoz is dedicated to providing high-quality, low-cost medicines to patients globally. The company fosters a culture of collaboration, diversity, and personal growth, making it an ideal workplace for ambitious professionals.
Job Details: Regulatory Affairs Specialist
- Job ID: REQ-10038006
- Location: Hyderabad, Telangana, India
- Employment Type: Full-time, Regular
- Functional Area: Research & Development
- Shift Work: No
Key Responsibilities
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📱 Get More DetailsAs a Regulatory Affairs Specialist at Sandoz, you will be critical in ensuring compliance with regulatory requirements and maintaining product licenses. Your responsibilities will include:
- Achieving optimal product registration with commercially attractive labelling aligns with the registration plan.
- Maintaining and securing product licenses in compliance with local regulations, company strategy, and global standards.
- Ensuring adherence to NP4, KRPIA code of conduct, and relevant laws for CPO activities, including DRAGON updates, RMP, packaging materials, and promotional activities.
- Building and maintaining strong relationships with internal and external stakeholders.
- Reporting technical complaints, adverse events, and special case scenarios related to Sandoz products within 24 hours of receipt.
- Managing the distribution of marketing samples (where applicable).
Qualifications and Skills Required
To be considered for this role, candidates must meet the following requirements:
Essential Requirements:
- Education: A degree in Lifesciences or a related field.
- Experience: Minimum of 2 years of experience in regulatory affairs or a similar role.
- Functional Breadth: Demonstrated ability to manage cross-functional projects.
- Cross-Cultural Experience: Experience working in diverse, multicultural environments.
- Operations Management: Strong execution and operational management skills.
- Project Management: Proven ability to plan and execute projects effectively.
Key Skills:
- Analytical thinking and attention to detail.
- Knowledge of clinical trials and regulatory compliance.
- Strong collaboration and communication skills.
- Proficiency in project planning and execution.
Commitment to Diversity and Inclusion
At Sandoz, diversity and inclusion are at the core of our values. We are dedicated to building teams that reflect the communities and patients we serve. By fostering an inclusive environment, we empower our employees to bring their unique perspectives and ideas to the table.
How to Apply
If you meet the qualifications and are excited about the opportunity to join Sandoz as a Regulatory Affairs Specialist in Hyderabad, apply now!
Apply Here: Sandoz Careers – Regulatory Affairs Specialist
Frequently Asked Questions (FAQs)
What is the job location for the Regulatory Affairs Specialist role?
The job is located in Hyderabad, Telangana, India.
What qualifications are required for this role?
Candidates must have a degree in Lifesciences or a related field and at least 2 years of experience in regulatory affairs.
Is this a full-time position?
Yes, this is a full-time, regular employment opportunity.
What are the key skills needed for this role?
The role requires strong analytical skills, project management expertise, and knowledge of regulatory compliance and clinical trials.
To apply for this job please visit www.sandoz.com.