R&d Master Data Originator Job in Procter & Gamble

Job Location

Job Description

Overview of the job/company

From its foundation 185 years ago as a soap and candle start-up, P&G today is one of the most successful consumer goods manufacturers in the world. We are home to iconic, trusted brands that touch 5 billion consumers worldwide and make life a little bit easier in small but meaningful ways.

In our production sites, products are manufactured for the entire global market. Using the latest high-tech control and manufacturing technology, we are expanding our leading market position in almost all markets in the world.

Our people are our greatest asset: with our philosophy of promotion from within, we are committed to finding and fostering world-class talent. Learn from our inspiring leaders, shape our supportive and welcoming culture, and place your personal development at the core of your work!

This is an exciting position within Personal Healthcare known for brands such as Vicks, Neurobion etc., from both technical and managerial point of view, that provides close collaboration with multi-functional technical teams while being on the digital site.

Your team

You will join a multi-national organization, a vibrant team and dynamic business environment on the journey toward the digitalization where high quality of data in core technical R&D systems is key in delivering product innovations.

Responsibilities of the role

As R&D Master Data originator Asia, Middle East & Africa (AMA) Personal Healthcare you will be responsible for:

• Driving implementation of R&D data standards in AMA region defined by global technical standards system owners in compliance with SOPs and guidelines
• Having very good understanding of the product data life cycle system processes such as change control, vendor set ups (ARAVO), SAP and PASS
• Assuring data completeness for incoming project requests covering all range of projects from base business as well as new initiatives, as well as verifying request related change control content and its status required for execution
• Following up with Technical Content Owners on missing data attributes/documents
• Origination of complex product and packaging specifications and automation requests in PLM system
• Performing all validation checks such as CA, BOM set ups (W&D), POA availability, for interdependent systems data flows
• Assuring availability of needed route templates for review and approval
• Pushing/routing created specifications and documentations into review and approval (validate requirements vs AMAT guidance)
• Assigning parts to correct libraries, maintaining master parts libraries
• Following up on missing R&A when due (system due date)

Role Requirements

We are looking for a passionate candidate with a strong sense of responsibility and accountability as well as attention to detail on the job. Good organization, collaboration and communication skills, both verbal and written, will be a plus when leading system implementation of projects and programs across all PHC (Personal Healthcare) brands and sites (incl. Contract Manufacturers) in AMA regions. Previous working knowledge of any commercially available master data system, skills in Microsoft Power Platforms (PowerApps, Power BI etc.) and experience in pharmaceutical/regulated industry would be a strong asset for this role. Advanced level of English and strong analytical thinking and problem-solving mindset is a must.

Job Qualifications

Graduation in Science or B. Pharm

Min exp 1-3 years

Preferably from Healthcare or Pharma industry