Leben Life Sciences Pvt. Ltd. (LLS), a renowned pharmaceutical formulation company with over 40 years of industry experience, has opened a fantastic career opportunity for fresh M.Pharm graduates. Located at their EU-GMP approved manufacturing facility in Akola, Maharashtra, this walk-in interview invitation is the perfect gateway for enthusiastic individuals aiming to build a career in the dynamic field of Regulatory Affairs.
About Leben Life Sciences Pvt. Ltd.
Leben Life Sciences has long been a trusted name in the pharmaceutical sector, known for its high-quality formulations and strict adherence to global regulatory standards. Their Akola facility, compliant with EU-GMP guidelines, showcases their commitment to quality and innovation. The company fosters a collaborative work culture that encourages professional growth and continuous learning.
Trainee Regulatory Affairs Role Overview
This entry-level role is tailor-made for fresh M.Pharm graduates keen on gaining practical experience in regulatory affairs. As a Trainee, you will work closely with seasoned professionals and be involved in vital regulatory functions that impact the company’s product approvals and compliance worldwide.
Job Location & Interview Details
- Location: Akola, Maharashtra (On-site)
- Interview Date: Wednesday, May 7th, 2025
- Interview Time: 9:30 AM to 10:30 AM
- Venue: Leben Life Sciences Pvt. Ltd., Plot No. C-20/1 & C-21, Phase III, MIDC, Akola, Shivar, Maharashtra
Candidates should bring an updated resume and relevant documents to the walk-in interview.
Key Responsibilities
The regulatory affairs trainee role involves supporting various regulatory processes that ensure the company’s pharmaceutical products comply with legal and quality standards:
- Assisting in the preparation and submission of regulatory documents to local and international authorities.
- Maintaining regulatory files and ensuring accurate record-keeping.
- Supporting the development and implementation of regulatory strategies aligned with evolving guidelines.
- Conducting research and analysis on regulatory policies and requirements applicable to pharmaceutical products.
- Collaborating effectively with cross-functional teams, including production, quality assurance, and R&D, to guarantee regulatory compliance throughout product lifecycles.
Ideal Candidate Profile
- Educational Qualification: M.Pharm degree from a recognized university.
- Experience: Freshers are encouraged to apply; no prior experience necessary.
- Skills: Strong attention to detail, excellent organizational skills, proficiency in Microsoft Office Suite.
- Attributes: Highly motivated, quick learner, ability to work independently and in teams, enthusiasm for a career in regulatory affairs.
Why Choose Leben Life Sciences?
Choosing to start your regulatory affairs career with Leben Life Sciences offers several benefits:
- Growth Opportunities: The company invests heavily in employee development and promotes internal career progression.
- Collaborative Work Environment: You will work alongside experienced professionals who are supportive and ready to mentor fresh talent.
- Industry Leadership: Join a company with a strong reputation for quality, innovation, and global compliance.
- Global Standards: Gain hands-on experience in an EU-GMP approved facility that adheres to some of the most rigorous manufacturing standards worldwide.
How to Prepare for the Interview
- Review basic concepts of pharmaceutical regulatory affairs, including document types and regulatory bodies.
- Be ready to discuss your academic background and any relevant projects or internships.
- Demonstrate your eagerness to learn and your attention to detail.
- Prepare questions to ask about the role and company to show your genuine interest.
Conclusion
For fresh M.Pharm graduates, the Regulatory Affairs Trainee position at Leben Life Sciences offers an excellent platform to launch a rewarding career in the pharmaceutical industry. The walk-in interview on May 7th, 2025, provides an immediate opportunity to join a reputable company known for quality and compliance. If you are motivated, detail-oriented, and eager to grow professionally, this role is your chance to gain valuable industry exposure and build a strong foundation in regulatory affairs.
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