• Gender: Male
• Age: 31
• Designation: Asst. Manager
• Highest Education Level: Diploma
• Preferred Country: India
• Preferred Location: New Delhi
• Work Experience: 12.1 Year(s)

Education

Diploma (Ceramic and Glass technology) from Government Polytechnic, Jhajjar (2009-2012).
Xth CLASS with HBSE syllabus with an aggregate of 83% from Bal Bharati high school (2009)
XII CLASS (SCIENCE) with an aggregate of 60% from NIOS (2011).
B.Tech in Mechanical Engineering from MDU

Skill Sets

7QC tools,
SPC (statistical process control).
5s team member
Certification of First Aider
Certification of Fire and safety's
Lean-Six Sigma Yellow Belt Certified
Lean-Six Sigma Green Belt Certified
Pursuing Black Belt Certification

Work Experience

Asst. Manager
From -2018 to till date
Company profile - Manufacturer & Supplier Of Glass Bottles, Vials Pharmaceuticals, Cosmetic Items & Bottles

Senior Inspector In Quality Control
From -2012 to 2018
Company profile - automated glass manufacturing

Job profile -
Height gauge (digital & analog)
Profile projector
Vernier caliper (digital & analog) and Micrometer
Thickness machine (AGR, MAGNA MIKE)

Job profile -
To ensure each and every processing stage of molded vials are meeting the Quality Standards.
To ensure all the Quality Operations are carried out as per Defined Standard Operating procedures.
Effective Hot End and Cold End communication for reducing the defects online.
Shift wise reporting and resolving quality related issues.
Planning, scheduling the IPQC and Batch Release shift priorities.
Qualification of Sorters & Final Checkers.
To Prepare Limit Sample job wise and as per specific customer.
Establish cGMP-GDP measurement of Process Capability (Cpk).
Reduce the SQC failure rejection rate from preceding year.
Effective Batch Management by ensuring all the operations are adhered to standard specifications from raw material to product dispatch of each batch.
Maintain Batch Records and control samples are stored in designated location for a defined storage period.
Address all the Quality Operations issues to the concerned section heads for taking necessary Corrective & Preventive actions.
Cross verify all the Quality Operations Corrective & Preventive Actions are effectively implemented.
Reviews all batch manufacturing and packaging records for correctness, completeness, and compliance to GMP standard.
Release the batch internally to warehouse through Material Clearance Note after reviewing all documents to be sure there are no loose ends (missing signatures, open deviations) and also examines testing data to confirm that the product meets specifications.
Release the batch commercially after ensuring the pre-dispatch report with certificate of Quality & receipt of internal batch release.
Utilize Quality tools to investigate & close the Non-conformities occurred during Batch Processing.
Follow-up Action Plans for process improvements, process deviations, Customers/auditors observations.