Neha Patole

To obtain a challenging position in the pharmaceutical industry where I can utilize my experience in GMP Documentation, QMS activities and production compliance along with my chemical engineering and process design engineering knowledge to continuous improvement. Seeking opportunities in QA, Production & Process Engineering

Doc. Chemist - Avik pharmaceuticals Ltd - Vapi, Gujarat

(2025-05)

• Preparation and review of procedure like SOPs, BMR, BPCR, ECR, and Protocol & Validation Documents
• Brief Knowledge of QMS elements like change control, Deviation Handling SCM activities
• Reviewed of completed BPCR, ECR and related documents
• Preparation of Training calendar of staffs and workers and Job responsibility
• Coordination employee training programs and maintained training records
• Coordinate induction training and periodic GMP training Records
• Preparation of shift schedule of staff and workers for every month
• Preparation of KSM data analysis
• Preparation of documents required by President-Operation

GMP Coordinator - Swadev Chemicals Pvt. Ltd - Vapi, Gujarat

(2022-04 - 2025-05)

• Reviewed completed BMRs, BPRs, ECRs and production records
• Reviewed & maintained departmental logbooks
• Prepared & revised SOPs in compliance with GMP requirements
• Handled change control documentation activities
• Plant round observation
• Calculated raw material consumption & monthly production yields
• Verifying the labelling activity during Finished Goods Transfer

B.Tech. - Chemical Engineering - Department of technology, Shivaji University (2021)

Higher Secondary Certificate - Mahaveer College (2017)

Secondary School Certificate - Shri Ram High School (2015)