Teva Pharmaceuticals Hiring Regulatory Affairs Associate I in Goa, India. Apply now for RA jobs in the pharmaceutical industry.
Teva Pharmaceuticals Hiring Regulatory Affairs Associate I – 2025 Career Opportunity in Goa
Teva Pharmaceuticals, one of the world’s largest and most respected manufacturers of generic medicines, is inviting applications for the position of Regulatory Affairs Associate I at its Goa facility. This opportunity is perfect for professionals with 2–4 years of experience in Regulatory Affairs, especially those who have worked with European and international markets. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
This role offers a chance to contribute to Teva’s global mission of improving access to affordable, high-quality medicines. As part of Teva’s regulatory team, you will play a key role in ensuring the company’s medicinal products comply with international regulatory standards and guidelines. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
About Teva Pharmaceuticals
Teva Pharmaceuticals, headquartered in Israel, is a global leader in the pharmaceutical industry and a trusted name in healthcare. With operations in nearly 60 countries, Teva employs tens of thousands of professionals committed to the same goal — making healthcare more accessible and affordable for millions worldwide. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
Every day, over 200 million people across the world take a Teva medicine, making the company one of the most significant contributors to global health and wellness. Teva’s product portfolio includes a broad range of generic, specialty, and over-the-counter (OTC) medicines, many of which appear on the World Health Organization’s Essential Medicines List. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
Working at Teva means being part of an organization that values integrity, innovation, teamwork, and a relentless commitment to quality.
Position Overview: Regulatory Affairs Associate I
- Position: Regulatory Affairs Associate I
- Company: Teva Pharmaceuticals
- Location: Goa, India – 403722
- Job ID: 63852
- Experience Required: 2–4 years
- Qualification: B.Pharm / M.Pharm
- Employment Type: Full-Time
- Department: Regulatory Affairs
- Reports To: Associate Director, Regulatory Affairs
This position focuses on preparing, compiling, and maintaining the CMC (Chemistry, Manufacturing, and Controls) sections of product dossiers (Modules 2.3 and 3) for global submissions. The Regulatory Affairs Associate will work under general supervision to ensure compliance with international regulatory requirements while collaborating with multiple departments to support product registrations and variations. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
Key Responsibilities
As a Regulatory Affairs Associate I, you will be responsible for various documentation, evaluation, and compliance-related activities essential to the success of Teva’s global regulatory operations. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
1. Dossier Compilation
- Prepare and compile Module 3 (Quality Section) and the corresponding Module 2.3 Quality Overall Summary (QoS) for submission to regulatory authorities or clients.
- Ensure all documentation meets regulatory and company standards for accuracy, completeness, and compliance.
2. Evaluation and Review
- Critically evaluate the content of CMC modules for completeness, clarity, and relevance in supporting new product registrations.
- Review and analyze change controls to determine the impact on regulatory submissions and define the filing category based on applicable guidelines.
3. Regulatory Submissions and Queries
- Compile and submit variation packages as required for regulatory changes.
- Coordinate responses to queries from regulatory authorities or clients, ensuring all stakeholders (internal teams and external suppliers) are involved in providing timely and accurate information.
4. Compliance and Documentation
- Maintain the department’s internal databases and tracking systems with updated information on submissions, approvals, and regulatory timelines.
- Ensure all activities comply with ICH guidelines, Good Manufacturing Practices (GMP), and company Standard Operating Procedures (SOPs).
5. Cross-functional Collaboration
- Act as a liaison between Regulatory Affairs and other departments across business units, including Quality Assurance, Manufacturing, and R&D.
- Ensure smooth communication and cooperation among internal teams to meet regulatory deadlines efficiently.
6. Continuous Learning and Development
- Stay updated on evolving regulatory requirements, industry trends, and pharmacopoeial changes across key markets (Europe, US, and Rest of the World).
- Participate in internal training sessions and workshops to enhance regulatory knowledge and operational excellence.
Required Qualifications and Experience
Candidates applying for the position should meet the following criteria:
- Educational Qualification:
Bachelor’s or Master’s degree in Pharmacy (B.Pharm/M.Pharm) from a recognized institution. - Experience:
Minimum 2 to 4 years of experience in Regulatory Affairs within the pharmaceutical industry, specifically involving European and international markets. - Technical Skills:
- Strong understanding of CMC documentation and global regulatory requirements.
- Familiarity with ICH guidelines and regional submission procedures.
- Good IT proficiency, including the ability to use regulatory databases and document management systems.
- Soft Skills:
- Excellent English communication skills (spoken and written).
- Strong organizational abilities and attention to detail.
- Ability to work effectively under general supervision while meeting strict deadlines.
- Collaborative mindset with a team-oriented approach.
- Proactive, responsible, and result-driven personality.
Why Join Teva Pharmaceuticals?
Teva offers an inclusive and dynamic work environment that encourages growth, innovation, and collaboration. Employees benefit from working in a global organization that combines technical expertise with a commitment to social responsibility. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
Key Benefits:
- Opportunity to work with one of the world’s top generic medicine manufacturers.
- Exposure to international regulatory markets and global product portfolios.
- Continuous professional development and skill enhancement.
- Supportive, ethical, and diverse workplace culture.
- Strong focus on employee well-being, health, and safety.
Work Environment and Culture
At Teva, every team member contributes to a shared mission of improving lives through better health. The company promotes a culture built on diversity, inclusion, collaboration, and respect. Employees are empowered to bring their ideas forward, ensuring innovation and efficiency in every area of operation. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
The Goa facility is known for its state-of-the-art infrastructure, advanced technology, and skilled professionals who drive the company’s regulatory and manufacturing excellence. Working here means being part of a team that values precision, quality, and accountability. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to maintaining an inclusive workplace that respects all individuals and provides equal opportunities for employment and advancement. The company strictly prohibits discrimination based on age, gender, religion, disability, nationality, or any other protected status. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
If you are contacted during the recruitment process, you can request accommodations to ensure an equitable and accessible experience. All such information will remain confidential and used solely to provide necessary support. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
Career Growth at Teva
This role provides a gateway to long-term career development within Teva’s Regulatory Affairs department. Successful professionals can advance to roles such as Senior Regulatory Affairs Associate, Regulatory Manager, or Global Regulatory Lead, based on performance, experience, and technical expertise. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
With Teva’s strong focus on mentorship, global collaboration, and skill-building, this position is ideal for candidates who aspire to make a meaningful contribution to the pharmaceutical industry while expanding their professional horizons. Teva Pharmaceuticals Hiring Regulatory Affairs Associate I
How to Apply
Interested and eligible candidates can apply for the Regulatory Affairs Associate I position at Teva Pharmaceuticals by following the steps below:
- Prepare an updated resume/CV detailing your educational qualifications, professional experience, and relevant skills.
- Include a brief cover letter explaining your motivation to join Teva and your suitability for the Regulatory Affairs role.
- Visit the official Teva Pharmaceuticals Careers Page to find the job listing (Job ID: 63852) and submit your application online.
📍 Location: Goa, India – 403722
🌐 Official Website: https://www.tevapharm.com
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