Our client, a multinational pharmaceutical industry, based at Cork location is looking for a “Senior Data Analyst” to join them for initially 12-month contract. As a Large Molecule Master Data Specialist, you’ll be responsible for the timely, efficient and accurate coordination, creation and maintenance of various master data elements (e.g. Material Master, BOM/Recipes, Production Versions, (time) standards, relationships and offsets, resources) in SAP/ECC and OMP+ and the execution of impact analyses or feasibility studies of change requests so that material planning, production, release, finance, or other processes can proceed optimally.
Essential Job Duties and Responsibilities
- Performs an assessment of the technical feasibility of change requests and/or introduction of new products based on input documents and in-depth technical system knowledge and possibly by conducting tests in a development environment
- Manages and processes various master data elements in ECC and OMP+:
- Initiates (technical) changes to the systems
- Critically checks supplied data, checks against (technical) specifications and instructions
- Performs Master Data creations / changes right first time in accordance with the applicable procedures and input supplied
- Becomes the point of contact for troubleshooting and root cause analysis on Master Data related issues.
- Performs various ad hoc tasks regarding Master Data Management:
- prepares, or adjusts, Master Data work instructions, guides new data managers & provides hands-on training, performs user acceptance tests, supports and concretizes global initiatives concerning Master Data in Sustain SAP and in OMP+
- Participates in or initiates actions to improve master data processes taking cGMP and lean principles into account, complies with cGMP and Safety regulations and actively supports site-related initiatives regarding e.g. safety, health, environment, Credo, D&I, Faster Forward, Cost Saving
- Coordinates master data management changes at the site supporting large projects impacting the systems’ setup of data.
- In this role you will work closely with other departments (e.g. Planning (MPS, DSS, MRP), Operations, Tech Ops, Process Engineers, Bio-TD, Finance, Warehousing, Quality Assurance) for coordinating and monitoring implementation data of various Master Data.
- A minimum of a Bachelor’s/University degree or equivalent and 2 years+ experience is required. APICS and Green Belt certification is preferred.
- Strong experience and thorough knowledge, preferably within the health care or FMCG industry.
- Good understanding of Data processing systems (e.g. SAP required, OMP+ preferred), procedures for processing and managing Master Data and production and / or lab processes.
- Experience working in GxP/GMP requirements.
- Ability to correctly perform impact analyses and/or (technical) feasibility studies and critically test the correctness of a multitude of data coming from multiple departments
- Ability to process, follow up and extract various data from various systems (query – use and possibly writing)
- Acquire the overview of and manage accurately a multitude of data
- Ability to give the right priority when processing data (first support for the most urgent processes)
- Collaborates effectively, strong communication skills
- Strong analytical and quantitative skills
- English fluently required, Dutch language skills an advantage
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Role:Salary: Daily Rate
Contact: Vandana Sharma