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S/4 Hana Qm Implementation Lead Resume

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PROFESSIONAL SUMMARY:

  • 24 years of professional experience which includes 16 years in SAP and worked primarily in the domain of Quality Management. This is backed with over 8 years of domain experience of Pharmaceutical Manufacturing Industry.
  • Experience on End to End implementation, Roll out, Support and Upgrade projects.
  • Quality experience in all aspects of project work: Design, Configuration, Unit testing, Integration testing, Documentation, Conversion/Migration, End user Training and cutover, hyper - care and support
  • Expertise in Inbound and outbound interfaces for seamless SAP integration with Labware LIMS, Star LIMS
  • Strong functional understanding of Integration points with MM, WM, PP, SD and FICO.
  • Strong knowledge on data mapping, creating QM master data, writing and presentation of training documentation
  • Proficient in conversion of business requirements into functional specification and technical specification for solution design, development, unite and integration testing and other aspects of software development life cycle.
  • Custom designed solutions for Large International Clients.
  • Strong problem-solving skills, analytical skills and ability to make balanced independent decisions
  • Excellent communication and Interpersonal skills.
  • Strong Classroom Management Skills
  • Industries supported Pharmaceutical, Chemical, Personal Care products, Medical devices & diagnostics, Food, Itanium Oxide & Liquid Crystal Business Unit, Auto spare manufacturer, Truck manufacturer, Pencil Manufacturing, Diamond manufacturing, Auto Engineering, Soap manufacturing, Confectionary.
  • Possesses good analytical and troubleshooting skills. Ability to manage team of consultants. Good Team Player.
  • Excellent Training Skills

SKILL:

  • S/4 HANA - Quality Management
  • S/4 HANA - Batch
  • Management
  • S/4 HANA - Integration points with MM, WM, PP and SD

TECHNICAL SKILLS:

Specialization: S/4 HANA QM CONSULTANT

ERP version: SAP 4.6, 4.7, ECC 6.0

Tools: HPQC, Solution Manager, Remedy, Share point, SOLID

Siemens Tools: RBE+ Reverse Business Engineering

IBM Tools: IBM Solution Builder, IBM Rational ClearQuest IBM Rational Portfolio Manager, IBM Rational ClearCase Knowledge Management Portal

PROFESSIONAL EXPERIENCE:

Confidential

S/4 HANA QM Implementation Lead

Confidential

Project Manager - Plan & Build Team

Confidential

SAP QM Consultant

Confidential

QM Lead Consultant

Confidential

Global Support Engineer - Lead QM/PP/MM/WM

Confidential

AMS support QM Lead consultant

Confidential

Data Conversion Functional Consultant

Confidential

AMS Support QM Consultant

Confidential

Offshore QM Consultant

Confidential

Lead Consultant QM/PP - Enhancement factory

Confidential

Business Impact Assessment Consultant

Responsibilities:

  • Temperature condition storage condition
  • Minimum remaining shelf life
  • Total shelf life
  • Period indicator for shelf life
  • Rounding rule for SLED
  • Batch management
  • QM Material authorization (digital signatures)
  • GR processing time
  • Inspection interval
  • Plant specific material status
  • QM procurement activation
  • QM Control keys
  • Certificate types
  • Inspection Setup, Multiple specification (Country / customer specific limits), control Inspection lot setup, Average inspection duration, Q-score procedure, Individual QM order,
  • Catalogs
  • Selected set
  • Master inspection characteristics (Qualitative / Quantitative)
  • Reference characteristics
  • Inspection method
  • Sampling procedure
  • Sampling scheme
  • Sample drawing procedure
  • Dynamic modification Rule
  • Quality work center
  • Inspection Plan
  • Client setup
  • Maintain setting at plant level
  • Define Control keys
  • Define keys for certificate processing
  • Define delivery block
  • Define status of supply relationship
  • Define Number ranges for Inspection characteristics, inspection methods
  • Assignment of Task list types to material types
  • Define Task List Usages
  • Define Task List status
  • Maintain parameters for Task list types
  • Maintain Number ranges for Inspection Plan
  • Define Inspection points
  • Define Object types for multiple specification
  • Define Objects for multiple specification
  • Define Control Keys for Inspection operation
  • Maintain Inspection Types
  • Maintain Inspection lot origin and assign inspection types
  • Maintain Number ranges for inspection lot
  • Deactivation of Quality Inspection for movement types
  • Define follow-up actions
  • Define Inventory postings
  • Define Usage decision codes
  • Define User status Profile
  • Define Number ranges for sample management
  • Define print control, form and print programs
  • Define configuration for copy of inspection results
  • Define notification types
  • Define Number ranges for notification types
  • Define sample container for stability studies
  • Define storage condition for stability studies
  • Define Material authorization group
  • Define Authorization group for QM Master data
  • Define defect classes
  • Define User fields - Operation (Inspection plan)
  • Define Task list usage
  • Define Organizational area
  • Update Standard characteristics LOBM*
  • Define Temperature conditions
  • Define Storage conditions
  • Activation of batch number assignment
  • Batch number range maintenance
  • Assignment of inspection type to Delivery Type for Customer returns
  • Goods receipt inspection - procured material
  • Source Inspection
  • Goods receipt inspection - subcontracting
  • Goods issue inspection
  • In-process Inspection
  • Goods receipt inspection - manufactured material
  • Early Inspection Lot - manufactured material
  • Other Goods receipt inspection
  • Inspection for customer returns
  • Vendor audit inspection
  • Stock transfer inspections
  • Recurring inspection
  • Inspection for delivery to customer with order
  • Inspection for delivery to customer without order
  • Inspection of physical samples
  • Stability study inspections
  • Stability Study - Trends
  • Other Inspections
  • Quality Info Records
  • AMPL/MPN – Approved Manufacturer Part List – Manufacturer Part Number
  • Quality Notifications – Vendor/Customer/Inhouse
  • Quality Notification – Stability Studies
  • Designed and Configured Statistical Process Control (SPC) and Dynamic modification rule.
  • Configured and Implemented Quality Certificates
  • Configured certificate profiles and implementation of certificates of analysis
  • Designed and Configured Dynamic Modification Rule, Quality Level for the Dynamic Modification of the Inspection Scope
  • Batch determination – FIFO / FEFO / LIFO
  • Batch Derivation – Sending & Receiving
  • Batch search strategies
  • DMS – Document Management System
  • SNC Collaboration Experience with Quality Management
  • Interfacing with g-QTS Track-wise
  • LIMS Interface (Labware/Star LIMS)

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