• Gender: Male
• Age: 26
• Designation: Quality Assurance, Quality Control.
• Highest Education Level: Graduate - Degree
• Preferred Country: India
• Notice Period: 30  Days
• Preferred Location: Ahmedabad
• Work Experience: 6.1 Year(s)

Education

Bachelor of Science (2016-2019) Govt. Madhav Science College, Ujjain (Govt. Vikram University Ujjain)

Diploma In Computer Application (2017-2018) Omega Solutions Institute Ujjain MP

Higher Sec. School Certificate (HSS) ( 2014-2016) Govt. Higher Sec. School Soyat Kalan and Passed out HSSC with 74.33 % from MPEB.

High School Certificate (HSC)(2012-2014) Govt. Higher Sec. School Soyat Kalan and Passed out HSSC with 75.33 % from MPEB.

Skill Sets

Calibration
Validation
Verification
CGMP (Current Good manufacturing practice)
GDP (GOOD DOCUMATION Practice)
GLP (GOOD LABROTERY Practices)

Work Experience

Quality Assurance, Quality Control.
From 30 March 2021 to till date.
Company Profile- Plastic packaging solution provider in the global pharma space.

Job Profile-
Quality Assurance
External and Internal audit handling.
QMS documents handling
New joining and all employees provide training.
SOP, STP and Specification preparation and distribution of Master documents.
Superseded documents handling and destroy of controlled copy.
Handling of controlled copy documents.
Qualification Protocol (IQ, OQ, PQ) as AHU, IBM, IPQC & IPQA Analyst Q.As., Vision system, Compressed air Report Preparation and Approval.
Preparation of Calibration, validation schedule and check Report.
Control and calibration of all the instruments are available in the plant.
Assigning QA ID No. Instrument and Equipment.
Line Clearance, PSA, In process, Visual inspection Record, challenge test, Master label sheet, CCR, PDI, COC and COA monitoring and report approval.
Finished Product Release, Implementation and Monitoring
Batch Manufacturing Record (BMR) Review and Approval.
Batch Numbering System and Batch Reconciliation Monitoring.
Machine Parameters Record and Process Parameter record Approval.
Pest Control Activity Schedule monitoring and New Mould Verification.
RM and FP Control Sample Monitoring and Destruction.
Monitoring Proper FIFO System.
Implementation and Monitoring QMS, GMP, GDP, and GLP.
To generate indent for requirements of stationary, new instrument, testing of material, finish product and calibration of instruments by external agency.

Quality Control
Implementation and Monitoring GMP, GDP, and GLP.
In-process Product Quality approval.
Daily In-process Checking Report Review and Approval.
Preparation of Standard Testing Procedure and Specification.
Checklist List of Incoming RM and PM Approval.
Finished Product Annually and Quarterly Testing Schedule Monitoring.
Raw Material Regular and Quarterly Testing Monitoring.
Retest Raw Material and Finished Product Policy Monitoring.
Sampling of Raw Material, In-process and Finished product samples.
Sending samples RM and FP for Testing to Centralize Lab.
Verification of outside Testing RM and FP Analytical Report.
Sealing and Leak Test Report Approval.
Assigning QC Reference Number Monitoring.
Raw Material Sampling approval and Labeling Process Monitoring
Ability to train reporting team members / co-workers.
Preparation and review of SOP/STP/COC/COA/Specification.
Preparation of Test Data Sheet for Raw Material, In-process samples and finishedproduct.
Review and evaluation analytical reports.
Analytical Report compilation for Raw Material & Finished product.
Calibration/Verification of Analytical and Weighing balance for QC, Production and warehouse.
Approved/Rejection label print, sign and past on the respected batches.

Executive IPQA
From 26 July 2019 to 27 March 2021
Company Profile- Plastic packaging solution provider in the global pharma space.

Future Goals

To secure a challenging position in a reputable organization to expand my learnings, knowledge, and skills. Secure a responsible career opportunity to fully utilize my training and skills, while making a significant contribution to the success of the company.