Regulatory Affairs Associate at Dr. Reddy’s Laboratories, MSc Lifescience/ Biotech candidates can apply!
Company Description: Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company that provides access to affordable and innovative medicines globally. With over 24,000 employees, we are committed to accelerating healthcare solutions because Good Health Can’t Wait. Established in 1984, we have grown to have a presence in 66 countries, focusing on access, affordability, and innovation in pharmaceuticals. Dr. Reddy’s promotes a diverse and inclusive work environment and is an equal opportunity employer.
Job Summary: We seek a Regulatory Affairs Specialist to manage regulatory submissions, product lifecycle activities, and quality management. This role involves collaborating with internal teams to ensure compliance and successful audits.
Roles & Responsibilities:
- Support the preparation and publishing of regulatory submissions.
- Manage product lifecycle activities such as variations and renewals.
- Review source documents for regulatory dossier authoring.
- Support internal and external audits and implement CAPA measures.
- Develop and maintain internal and external networks.
- Perform other duties assigned by the supervisor.
Qualifications:
- Educational Qualification: Master of Science in life sciences, Biotechnology, or related field.
- Minimum Work Experience: 3-6 years in regulatory affairs.
Skills & Attributes:
- Knowledge of Regulatory guidelines.
- Proficiency in spoken and written English.
- Computer proficiency, including Google Applications and MS Excel.
- Strong interpersonal and communication skills.
- Attention to detail and ability to meet deadlines.
- Knowledge of Veeva Vault/Docubridge is a plus.
Benefits Offered: At Dr. Reddy’s, we prioritize your career growth with personalized learning programs. Our benefits package includes support for relocation, maternity & paternity benefits, medical coverage, life insurance, and continuous learning opportunities.
Keywords: Regulatory Affairs Associate, Dr. Reddy’s, Regulatory Affairs Specialist, Pharmaceutical Company, Regulatory Submissions, Product Lifecycle Management, Compliance, Audits, Regulatory Guidelines, Biotechnology, Multinational, Healthcare Solutions.CAPA, Veeva, Vault, Docubridge, Dr., Reddy’s Laboratories, Quality Management Experience Applications, Google, Excel.
