RESUME

PAVAN KUMAR.L

Flat No.***, Cecon, La Gardenia Apartment

Pragathi enclave, Miyapur * : adp0an@r.postjobfree.com

Hyderabad 500049, Telangana ( : +91-964*******.

Career Objective:

Seeking a challenging and rewarding career as SAP QM professional where I can contribute my knowledge and skills for growth and development of the organization and to be able to implement solutions that meet the customer requirements using my variety of software development skills and technical expertise.

Professional Summary:

8 Years of Domain experience and 6 years of functional consultant experience in SAP PP and QM Module.

Experienced in implementation of two Full Life Cycle Implementations and one Support Projects in SAP ECC 6.0 and 7.4.

Having good experience in Reports, Interface, Enhancements and Forms.

Prepare the configuration document having the configuration changes and functional specification document containing the development requirements.

Prepare Unit test document after the successful testing once the development is completed.

Responsible for integration testing, UAT and fixing the issues raised by users either in UAT or after go live and during hyper care.

Proficient in business process study, gathering requirements, process design, configuration and development, preparation of functional specifications, testing processes, quality processes, end user training and documentation.

Having good experience on charm process and solman.

8 years of domain experience in Quality control with roles of testing of raw materials, semi-finished materials, finished materials, packing material. Performing results recording for Inspection lots, usage decision and stock posting. Calibration and troubleshooting of analytical equipment’s, stability study, conducting internal audits, review of QMS activities.

Possess excellent multitasking skills and ability to make confident and independent decisions with good analytical and problem-solving skills.

Strong domain and functional experience in customizing, configuring, Integrating and testing.

Integration knowledge of QM-MM, QM-PP, QM-PM & PP-SD, PP- MM, PP- QM, PP- SD & PP- PM.

Strong Supporting experience in Quality management includes Quality Planning, Quality Notifications, and Quality Inspection.

Strong supporting experience in Production planning includes Master data, S and OP, Demand management, Production order execution, Batch management, Discrete manufacturing, REM, Process industries.

Strong supporting experience in Quality management includes creation of master data like Material master, Inspection Plan, Inspection types, MIC’s like qualitative and quantitative, calculated characteristic, conditional characteristic, catalogs, selected set, material specification, batch management. Results recording, usage decision, Stock posting, Inspection during production like time based intervals, quantity based intervals, freely defined intervals. Quality inspection at the end of the production process, defect recording, creation of quality notification during defect.

Strong Supporting experience in master data includes Material master, BOM, work center, routing, production version, Sales and Operational Planning includes standard SOP and Flexible planning, Demand management includes make to order (10,11,40) and Make to Stock(20,50), Batch management, REM, PP-PI and Discreet manufacturing.

Handling of other software’s like LIMS (Caliber), DMS (Metric Stream), Empower 2 &3 with audit trail and Lab Solution.

Experience in Production-Process industry and Repetitive Manufacturing.

Extensive expertise in Configuration, Development, Testing, and user defined Reports in QM.

Part of a team to gather business requirement and had closely worked with the solution owners to understand and provide them the feasible solution.

Good knowledge on planning strategies like Make to Stock and Make to Order.

Good knowledge of manufacturing types like Discrete, Repetitive and Process industries.

SAP Expertise:

Working as a Functional Consultant in SAP PP/QM in various phases of SAP implementation, Configuration, Integration with MM and SD.

Part of 2 full life Cycle Implementations and one supporting Project.

Worked on automatic Quality notification creation when Customer created Quality Notification.

Worked on custom reports like sending offline COA to the customer.

Worked on Idoc to send COA to the customer when POD is done.

Worked on sending automatic E-mail alert when Inspection lot and quality notification is created.

Worked on notifying relevant partners to approve or reject when quality notifications are overdue.

Worked on triggering automatic Email alert when production order released and TECO.

Good experience in process industries, PI sheets, control recipe, process messages.

Experience in various phases of project Implementation like requirement gathering, development, documentation, testing. Also having experience in maintenance/support project.

Have positive attitude and proven to work well with individuals at all levels and ability to work under pressure.

Keen to learn new technologies.

Having good knowledge on SAP production planning like master data, BOM, routing, work centre, product version, creation of production order and Convert material from one type to another type. Download master data to excel.

Roles and Responsibilities:

Responsible for the configuration of SAP PP/QM area to meet the business requirement to enhance the quality management process.

An ability to solve complex problems quickly and creatively.

Strong domain and functional knowledge of Quality Management processes and techniques with a confident approach and excellent communication skills.

Configuration of new action items in Notifications and implemented new functionalities for them as per business requirement.

Work Experience:

Role

SAP Sr Consultent

Organization

Tech Mahindra

Duration

9 months (02/2021 - Till date)

Team Size

10 Members

Tech Mahindra is an Indian multinational technology company that provides Information Technology and Business Process Outsourcing services.

Project-1:

Client: Sadara Chemical Company

Duration: 02/2021 to till date

Type of Project: Implementation

Achievements for PP/QM:

Strong Implementation experience in creating Design document, configuration, functional specs and Unit test document which suits the business needs.

Developed customer specific repot like offline COA, Online COA through IDOC and Quality Certificate.

Prepared test scripts for integration testing and prepared test data for user acceptance testing.

Supported in resolving the issues raised by the end users after analysing and discussing the issue with them and upon approval from them.

Configurations and customizations as per the customer latest requirements.

As a functional consultant in SAP QM/PP, involved in master data like material master, inspection lot(automatic and manual),Sampling Procedure, Sampling Scheme, Sample Drawing Procedure, Catalogue, Selected set, catalogue profile, Inspection plan, Inspection method, Master inspection characteristic like qualitative, quantitative, calculated characteristic, Conditional Characteristic, material specification.

In PP Involved in Master data like BOM, Resource, Master recipe, Product version. S and OP, Demand management, batch management, Batch determination, MPS and MRP.

Good Handling experience on Inspection Types like 01,02,03,04,05,06,08,09,10,14,15,16 and 89 according to business requirement.

Stock posting and usage decision process completed without entering results recording based on priority and Selecting automatic inspection select or deselect depending on requirement.

Created calculated characteristic for packing material

Created conditional characteristic when skip test is allowed.

Periodic Training of the end users

Solving end user issues on master data, Quality Planning, Quality Execution and other areas.

Role

SAP Consultent

Organization

Grapple Info Solutions Pvt. Ltd.

Duration

4.9 Years (01/2016 - Till Date)

Team Size

10 Members

Grapple Info Solutions empowers executives, developers, and business users with Fast Data solutions that make the right data available in real time for faster answers, better decisions, and smarter action. Thousands of businesses across the globe have relied on Grapple technology to integrate their applications and ecosystems, analyze their data, and create real-time solutions.

Project-1:

Client: Hetero Drugs

Duration: 01/2016 to 03/2018

Type of Project: Implementation

Achievements for PP/QM:

Strong Implementation experience in creating configuration and functional specs which suits the business needs.

Prepared test scripts for integration testing and prepared test data for user acceptance testing.

Supported in resolving the issues raised by the end users after analysing and discussing the issue with them and upon approval from them.

Configurations and customizations as per the customer latest requirements.

As a functional consultant in SAP QM/PP, involved in Master data like Material Master, inspection lot(automatic and manual),Sampling Procedure, Sampling Scheme, Sample Drawing Procedure, Catalogue, Selected set, Catalog Profile, Inspection plan, Inspection Method, Master inspection characteristic like qualitative, quantitative, calculated characteristic, Conditional Characteristic, material specification.

In PP Involved in Master data like BOM, Resource, Master recipe, Product version. S and OP, Demand management, batch management, Batch determination, MPS and MRP.

Good Handling experience on Inspection Types like 01,02,03,04,05,06,08,09,10,14,15,16 and 89 according to business requirement.

Good experience in planning strategies like Make to stock (10, 11 and 40) and Make to order (20 and 50).

Implemented triggering an automatic Email alert when Inspection lot and quality notification is created.

Implemented cancelling all purchase orders of a vendor, when a customer returns a product more times than a threshold and alert the purchasing and sales team.

Good experience on production planning for process industries, process instructions (PI) sheets, control recipe, Process messages, Control recipe destination, relations ships, process control systems.

Generation of control recipe, send control recipe to process control system, maintain PI sheet, sending process message to process order.

Automatic goods receipt and goods using PI sheets.

Good experience on By Product & Co Product.

Implemented notifying relevant partners to approve or reject when quality notifications are overdue.

Implemented triggering an automatic Email alert when production order released and TECO.

Client Specific report developments like Daily production report, Material Reconciliation report, Daily Quality report etc were developed.

Having good knowledge on creation of Production order, Convert material from one type to another type, download master data to excel.

Stock posting and usage decision process completed without entering results recording based on priority and Selecting automatic inspection select or deselect depending on requirement.

Created calculated characteristic for packing material

Created conditional characteristic when skip test is allowed.

Periodic Training of the end users

Solving end user issues on master data, Quality Planning, Quality Execution and other areas.

Project-2:

Client: Apollo Distilleries

Duration: 04/2018 to 02/2021

Type of Project: Support

Achievements for QM:

Work actively with team members to analyse and resolve application issues.

Worked on issue with customer received empty inspection lot data.

Worked on Quality notification Issues.

Strong supporting experience in fixing the defects without missing SLA.

Implemented change requests.

Master data creation like characteristic, class, assigning class to materials.

Batch determination procedure and rules.

Gave training on creation of BOM, Resource, Master recipe, product version.

Production order and shop floor control customizing and process orders.

PP-PI Process orders and process management.

Designation

Sr.Executive, QC

Organization

Hetero Drugs, Hyderabad

Duration

1 Year 3 Months (09/2014 – 01/2016)

Team Size

25 Members

The Hetero is one of India’s leading generic pharmaceutical companies and the world’s largest producer of anti-retroviral drugs. Hetero’s business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics.

Roles and Responsibilities:

Monitoring quality management service activities like deviation, change control and CAPA.

Preparation and review of SOP’s and STP’S.

Review of Deviation like planned and unplanned and provide CAPA.

Review of change controls and assigned to respected areas.

Conduction internal audits.

Investigation of OOS and OOT (Quality notification)

Provide product consistency by using Statistical process control, control charts.

Maintain Stability management.

Creation of calibration schedule.

Designation

Team member, QC

Organization

Dr. Reddy’s Laboratories

Duration

2 Year 1 Month (08/2012 – 09/2014)

Team Size

40 Members

The Dr. Reddy’s Laboratories is a multinational pharmaceutical company. it began as a supplier to Indian drug manufacturers, but it soon started exporting to other less-regulated markets that had the advantage of not having to spend time and money on a manufacturing plant that would gain approval from a drug licensing body such as the U.S. Food and Drug Administration (FDA).

Roles and Responsibilities:

Created inspection lots, results recording, usage diction, stock posing.

Created MIC like qualitative and quantitative using QS21

Created sampling Procedure by using QDV1 and Inspection methods by using QS31.

Created catalogs, selected set, and assigned catalog to selected set using QS41 and QS51.

Assigning inspection plan to material using QP01.

Change inspection type according to material.

Creation of calibration inspection (Test equipment management)

Creation of certificate profile and certificate printing.

Batch releases, investigation of market complaints by using Quality Notifications. Change controls, deviations and CAPA.

Created Physical samples like Primary samples, Pooled samples and reserved samples.

Print COA by using Quality Certificates and maintained Recurring Inspections.

Prepare PQR Document By using SPC.

Designation

Sr.Executive, QC

Organization

Virupaksha Organics Pvt.Ltd.

Duration

3 Years (09/2009 – 08/2012)

Team Size

15 Members

The Virupaksha Organics is a fast-emerging API manufacturer with diversified Global Presence and with state-of- art infrastructure. We are building a global specialty pharmaceutical products and developing a wide range of API’s from recombinant

Roles and Responsibilities:

Created inspection lots, results recording, usage diction, stock posing.

Analysis of Raw material, In-process, Finished Product, Reserve samples, Stability Samples.

Collection of physical samples from where house according to sampling procedure,

Calibration of instruments like HPLC, GC, pH meter, etc.

Preparation of SOP’s and STP’s, upload in DMS (Metric Stream)

Designation

Sr.Executive, QC

Organization

SRAAC Pvt.Ltd.

Duration

2 Years (10/2007 – 09/2009)

Team Size

10 Members

The SRAAC Limited is the flagship company of the TGV Group It is the leading producer of Chlor-Alkali products and also manufactures Castor Derivatives and Fatty Acids. Besides operating a commercial Power Project of 28MW.

Roles and Responsibilities:

Analysis of Raw material, In-process, Finished Product, Reserve samples, Stability Samples

Collection of physical samples from where house according to sampling procedure,

Calibration of instruments like HPLC, GC, pH meter, etc.

Preparation of SOP’s and STP’s, upload in DMS (Metric Stream)

Educational Background:

Master of Science (M.Sc) in chemistry from Sri Krishnadevaraya University, Ananatur.

Bachelor’s degree (B.Sc) in MPC from Sri Krishna Devaraya University.

Personal details:

Name : L. Pavan Kumar Rao

Father’s Name : L. Rama Mohan Rao

Date of Birth : 19th May 1985

Gender : Male

Marital status : Married

Languages Known : Telugu, English & Hindi.

Declaration:

I hereby declare that the above mentioned information is correct to the best of my knowledge.

Place:

Date: (Pavan Kumar Rao. L)

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