SAP Master Data Specialist
- Contractor
- Full-Time
- Devens, MA
- Splintpharma
- Prefferd visa: OPT, CPT, F1, H4, L2, J1, Have H1 Visa, Need H1 Visa, EAD, US Citizen
- Posted 3 years ago – Accepting applications
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Offerd Salary $ 30 - $ 40
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Required Position 2-4 hires
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Experience 0-3 Years Required
Core job description:
• Performs quality approval of routine SAP Master Data.
• Update Quality Master Data in SAP including inspection plans and Inspection Characteristics
• Assist in the start up of the Devens Cell Therapy facility, including:
o Assist in drafting Standard Operating Procedures (SOPs) and Work Practices (WPs) with management guidance
o Participates in business processes to monitor and track routine workload
• Works closely with supply chain, manufacturing, and QA Management with to escalate and report discrepancies in SAP processes.
• Other responsibilities as needed
Knowledge and skillset:
• Knowledge of science generally attained through studies resulting in a B.S., in science, engineering, biochemistry, related discipline, or its equivalent.
•Experience in Quality is desired.
• Ideal candidate is recommended to have a minimum of 6 years of directly relevant experience in a regulated environment.
• Prior evidence of successful participation on work/study teams where combined contribution, collaboration, and time bound results are expected.
• Demonstrated proficiency in common computer tools such as word processing, spreadsheet and web based applications, as well as ERP solutions such as SAP. Direct experience with SAP Master Data is highly preferred.
• Work/study experience where attention to detail and personal accountability were critical to success.
• Previous work experience where attention to detail and personal accountability were critical to success.
• Strong communication skills and the ability to follow written and verbal instructions.
Core job description:
• Performs quality approval of routine SAP Master Data.
• Update Quality Master Data in SAP including inspection plans and Inspection Characteristics
• Assist in the start up of the Devens Cell Therapy facility, including:
o Assist in drafting Standard Operating Procedures (SOPs) and Work Practices (WPs) with management guidance
o Participates in business processes to monitor and track routine workload
• Works closely with supply chain, manufacturing, and QA Management with to escalate and report discrepancies in SAP processes.
• Other responsibilities as needed
Knowledge and skillset:
• Knowledge of science generally attained through studies resulting in a B.S., in science, engineering, biochemistry, related discipline, or its equivalent.
•Experience in Quality is desired.
• Ideal candidate is recommended to have a minimum of 6 years of directly relevant experience in a regulated environment.
• Prior evidence of successful participation on work/study teams where combined contribution, collaboration, and time bound results are expected.
• Demonstrated proficiency in common computer tools such as word processing, spreadsheet and web based applications, as well as ERP solutions such as SAP. Direct experience with SAP Master Data is highly preferred.
• Work/study experience where attention to detail and personal accountability were critical to success.
• Previous work experience where attention to detail and personal accountability were critical to success.
• Strong communication skills and the ability to follow written and verbal instructions.