Mahendra Deshmukh
Trainee Senior Officer @Glenmark Pharmaceuticals
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WORK HISTORY
Trainee Senior Officer @Glenmark Pharmaceuticals
Mapusa, IN
Major Duties :Overseeing daily pharmaceutical manufacturing operations to ensure compliance with GMP (Good Manufacturing Practices).Supervising batch production and documentation in line with regulatory guidelines.Performing and Documenting Cleaning and Line Clearances.Coordinating with cross-functional teams (QA, QC, Maintenance) to maintain uninterrupted production flow.Monitoring equipment performance and ensuring preventive maintenance schedules are followed.Training and mentoring junior staff on SOPs, safety procedures, and regulatory compliance.Participating in internal and external audits and implementing CAPA (Corrective and Preventive Actions).Major Successes:Executed a Cleaning Validation protocol to include scrubbing time of the APCG Equipment and its parts in the Type-B cleaning checklist.Zero Line Clearance failure.
EDUCATION
Dr. Babasaheb Ambedkar Technological University (DBATU)
Bachelor of Pharmacy - BPharm, Pharmacy
Shoolini University
Master of Business Administration - MBA, Pharmaceutical and Healthcare Management
OYSTER INSTITUTE OF PHARMACY, AURANGABAD
Bachelor of Pharmacy - BPharm, Pharmacy, Pharmaceutical Sciences, and Administration
ABOUT MAHENDRA DESHMUKH
As a dedicated Pharmaceutical Science graduate, I am passionate about ensuring the highest standards of quality and safety in the production of pharmaceutical products. With a strong academic foundation in drug formulation, regulatory compliance, and manufacturing processes, I am eager to apply my knowledge to roles in Production, Quality Control and Quality Assurance within the pharmaceutical industry.Throughout my studies, I gained hands-on experience with GMP (Good Manufacturing Practices), analytical techniques, and the importance of maintaining stringent quality standards to meet regulatory requirements. I am particularly interested in contributing to the optimization of production processes, ensuring product consistency, and safeguarding patient safety by adhering to the highest quality assurance protocols.Key strengths include:• In-depth understanding of Pharmaceutical manufacturing processes and Quality control techniques.• Familiarity with regulatory standards (FDA,ICH) and GMP guidelines.• Strong problem-solving skills, attention to detail, and ability to work effectively in team environments.• Enthusiasm for continuous learning and staying updated on the latest industry advancements.I am eager to connect with professionals in the pharmaceutical industry to share insights, exchange knowledge, and explore opportunities where I can contribute to the development and manufacturing of safe, high-quality pharmaceutical products.Let’s connect!
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