Suraj Kumar
Quality Control professional with 6 years of experience in pharmaceutical manufacturing and laboratory operations
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نبذة
Results-driven Quality Control professional with 6 years of experience in pharmaceutical manufacturing and laboratory operations. Skilled in raw material analysis, finished product testing, stability studies, documentation, GMP compliance, and laboratory investigations. Experienced in handling HPLC, UV, dissolution, FTIR, and wet chemistry instruments.
Strong leadership ability with experience guiding QC analysts, maintaining data integrity, and ensuring compliance with WHO-GMP, EU-GMP, and MHRA standards. Seeking a position as QC Leader/QC Supervisor in a reputed pharmaceutical company in Dubai.
الخبرة
Quality Controller - Quest Vitamin Middle East Free Zone LLC - Dubai, UAE
(2022-04)
- Performed analysis of raw materials, in-process samples, finished products, and stability samples as per approved specifications.
- Operated and maintained analytical instruments including HPLC, GC, UV Spectrophotometer, Dissolution Apparatus, FTIR, and pH meter.
- Reviewed analytical reports and ensured compliance with GMP and laboratory SOPs.
- Investigated OOS and OOT results with root cause analysis.
- Assisted QC Manager in batch release activities and audit preparation.
- Maintained laboratory documentation in accordance with ALCOA+ data integrity principles.
- Trained junior analysts on analytical procedures and laboratory safety practices.
- Coordinated calibration and preventive maintenance activities for laboratory instruments.
- Reduced analytical report errors by 25% through improved review procedures.
- Supported regulatory audits with zero critical observations.
- Led laboratory workflow coordination during high production demand.
QC Officer - Akums Drug and Pharmaceuticals Pvt. Ltd. - Haridwar, India
(2019-01 - 2021-06)
- Conducted routine analysis of pharmaceutical products according to USP/BP/IP methods.
- Assisted senior analysts in chemical and instrumental analysis.
- Performed testing of raw materials and packaging materials.
- Prepared reports and maintained laboratory documentation.
- Prepared standard solutions, reagents, and volumetric solutions.
- Performed environmental monitoring and water analysis.
- Maintained instrument logbooks and analytical records.
- Supported method verification and transfer activities.
- Ensured laboratory cleanliness and compliance with safety standards.
- Improved sample turnaround time by 20%.
- Assisted in successful WHO-GMP inspection readiness.
التعليم
Master of Science - Chemistry - Dr. Ram Manohar Lohia Avadh University (2023)
Bachelor of Science - Chemistry - Dr. Ram Manohar Lohia Avadh University (2017)
