MSN Group is thrilled to announce a walk-in drive for experienced professionals in Formulation R&D – Technology Transfer! This is an exciting opportunity to join a dynamic team within the pharmaceutical and life sciences industry. If you’re a skilled and motivated individual with a passion for innovation, we encourage you to attend our walk-in interview.
Walk-In Drive Details: Your Path to a Rewarding Career
Date: Saturday, May 17th, 2025
Time: 9:30 AM – 3:00 PM
Venue: MSN Laboratories Pvt. Ltd, R&D Centre, Pashamylaram (Village), Patancheru (Mandal), Sangareddy District, Telangana.
Make sure to arrive on time with your updated resume and relevant documents. We look forward to meeting you and discussing how your skills and experience can contribute to our ongoing success. This is a fantastic chance to learn more about MSN Group, our innovative culture, and the numerous career progression opportunities available.
A Thriving Career in Formulation R&D – Technology Transfer
This position offers a full-time, permanent role within our Formulation R&D department, specifically focusing on Technology Transfer. You will be a key contributor to our ongoing efforts to improve and expand our pharmaceutical manufacturing capabilities. This role demands a high level of expertise and attention to detail, making it ideal for ambitious and dedicated professionals.
Role: Executive / Senior Executive
Department: Formulation R&D – FML (Technology Transfer)
Industry: Pharmaceuticals & Life Sciences
Employment Type: Full Time, Permanent
Eligibility and Qualifications: Are You the Right Fit?
To be considered for this exciting opportunity, we are looking for candidates with the following qualifications and experience:
- Qualification: B.Sc, B.Pharm, or M.Pharm. Candidates with advanced degrees in related fields are also encouraged to apply. We value a strong academic foundation and a demonstrated commitment to continuous learning.
- Experience: 2 to 7 years of experience in Formulation R&D and Technology Transfer is required. Successful candidates will possess a strong understanding of pharmaceutical manufacturing processes, quality control procedures, and regulatory guidelines. We are searching for individuals with a proven track record of success in a fast-paced, results-oriented environment.
Key Responsibilities: Making a Significant Impact
The successful candidate will play a critical role in several key areas, including:
- Batch Record Management: Preparation of accurate and compliant Batch Manufacturing Records (BMRs) and Batch Packing Records (BPRs) is paramount. This involves meticulous attention to detail and a deep understanding of Good Manufacturing Practices (GMP).
- Process Validation: Drafting and executing Process Validation protocols and reports, ensuring the consistent quality and efficacy of our products. This requires a strong understanding of validation principles and a commitment to data integrity.
- Process Optimization: Handling and maintaining documentation related to process optimization initiatives. This involves collaborating with cross-functional teams to identify and implement improvements to manufacturing processes.
- Quality Management System (QMS): Managing various QMS activities, including Change Controls, Out of Specification (OOS) investigations, Out of Trend (OOT) investigations, and Deviation management. This involves a proactive approach to quality assurance and a strong commitment to compliance.
Work Location: Investing in Our Future
Following a successful interview and selection process, the work location will be in Kothur, Mekaguda, Telangana. We offer a collaborative and supportive work environment, with ample opportunities for professional development and growth. This is more than just a job; it’s an investment in your future and the future of innovative pharmaceutical manufacturing.
