Regulatory Affairs Internship – Launch Your Pharma Career in Chennai!
Summary:
Levim Lifetech Pvt Ltd is seeking highly motivated and detail-oriented graduates to join our team as Regulatory Affairs Interns for a 6-month program in Taramani, Chennai. This is an exceptional opportunity for recent graduates and early-career professionals in Pharmacy, Life Sciences, or related fields to gain hands-on experience and build a strong foundation in regulatory affairs within the pharmaceutical industry. If you are eager to learn, contribute, and launch a successful career in this critical area, we encourage you to apply.
About Levim Lifetech Pvt Ltd:
[Insert a brief and compelling company description here. Focus on the company’s mission, values, and areas of specialization within the pharmaceutical industry. This is crucial for attracting candidates. Example: Levim Lifetech Pvt Ltd is a rapidly growing pharmaceutical company committed to developing and manufacturing innovative healthcare solutions. We strive for excellence in quality, safety, and efficacy, and we are dedicated to improving the lives of patients through our products.]
Job Title: Regulatory Affairs Intern
Location: Taramani, Chennai, Tamil Nadu, India
Duration: 6 Months
Department: Regulatory Affairs
Job Description:
As a Regulatory Affairs Intern at Levim Lifetech, you will be an integral part of our Regulatory Affairs team, gaining valuable practical experience in the core operations of this critical function. You will work alongside experienced professionals and contribute to ensuring our products meet all regulatory requirements for market approval and continued compliance. This internship offers a structured learning environment with opportunities to understand the complexities of regulatory dossiers, submissions, labeling compliance, and quality assurance.
Key Responsibilities:
- Submission Support: Assist in the preparation, compilation, and review of regulatory submissions, dossiers, and applications for various markets.
- Documentation Management: Support data collection, document formatting, and the management of regulatory documentation, ensuring accuracy and completeness.
- Cross-Functional Collaboration: Coordinate with various internal teams, including Quality Assurance (QA), Quality Control (QC), Production, Research & Development (R&D), and Pharmacovigilance, to gather necessary documents and information for regulatory submissions.
- Labeling Compliance: Review product artworks, labels, and packaging materials to ensure they comply with relevant regulatory guidelines and requirements.
- Administrative Support: Provide administrative and regulatory documentation support as needed, including maintaining databases, tracking submissions, and managing correspondence.
- Learning and Development: Actively participate in training sessions and seek opportunities to expand your knowledge of regulatory affairs principles and practices.
Qualifications:
- Educational Background: Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Chemistry, Biotechnology, or a related field.
- Attention to Detail: Exceptional attention to detail and accuracy in all tasks.
- Documentation Skills: Strong documentation skills, including the ability to organize, format, and maintain records effectively.
- Communication Skills: Excellent communication and interpersonal skills, with the ability to interact professionally with colleagues and stakeholders.
- Teamwork: Ability to work effectively as part of a cross-functional team.
- Learning Agility: A strong willingness to learn and adapt to new challenges and regulatory requirements.
- Computer Literacy: Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
Benefits:
- Stipend: ₹10,000 – ₹15,000 per month.
- Hands-on Experience: Gain practical, hands-on experience in Regulatory Affairs processes within a reputable pharmaceutical company.
- Mentorship: Work alongside experienced regulatory affairs professionals in a structured learning environment.
- Comprehensive Understanding: Develop a practical understanding of dossiers, submissions, labeling, and QA compliance within the pharmaceutical industry.
- Career Development: Opportunity to build a strong foundation for a successful career in Regulatory Affairs.
- Certificate of Completion: Receive a certificate upon successful completion of the internship program.
How to Apply:
Interested and qualified candidates are encouraged to submit their updated resume to [Email Address: [email protected]]. Please include “Regulatory Affairs Internship Application” in the subject line. We look forward to receiving your application!
Application Deadline: [Insert Application Deadline Here]
Levim Lifetech Pvt Ltd is an equal opportunity employer and values diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.