

Aequor
Business Analyst
β - Featured Role | Apply direct with Data Freelance Hub
This role is for an ERP Business Analyst II in Vacaville, CA (Hybrid) for 12 months+. Requires 3+ years GMP experience in biotech/pharmaceuticals, 5+ years SAP ECC master data experience, strong analytical skills, and proficiency in MS Office and BI systems.
π - Country
United States
π± - Currency
$ USD
-
π° - Day rate
Unknown
-
ποΈ - Date
October 1, 2025
π - Duration
More than 6 months
-
ποΈ - Location
Hybrid
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π - Contract
Unknown
-
π - Security
Unknown
-
π - Location detailed
Vacaville, CA
-
π§ - Skills detailed
#SAP #UAT (User Acceptance Testing) #Business Analysis #Databases #"ETL (Extract #Transform #Load)" #MDM (Master Data Management) #Data Lifecycle #Documentation #Compliance #BI (Business Intelligence) #Data Management #Strategy
Role description
Job Title: ERP Business Analyst II
Location: Vacaville, CA (Hybrid Role)
Duration: 12 months + will be extended.
Work schedule: Mon - Fri, only 3 days in a week.
Job Summary:
The ERP Business Systems Analyst II is responsible for all SAP attributes of the site Product and Quality Master Data Management throughout the data lifecycle.
Manages master data changes in the ERP (SAP) System.
SME for training of stakeholders/staff on standard and best practices.
Duties:
Partners with internal and external stakeholders within Supply Chain, Manufacturing, Technology, Quality and Finance organizations to implement the production master data lifecycle in SAP (design, develop, deploy, maintain, optimize, audit, and retire).
Maintains a high-level understanding of the data related business processes and systems within/ outside the ERP system landscape to ensure SAP data domain compliance/ alignment.
Create, mature, maintain, and retire SAP Master Data Objects related to Production and Quality Data. This includes, but is not limited to Material Masters, Recipes, Bill of Materials, Resources, Master Inspection Characteristics, Info Records and ancillary support/ table data.
Create, mature, maintain, and retire SAP Master Data Objects related to Quality Management (QM) Data. Including Direct Material data, Inspection Plans, Sampling Schemes, Draw Procedures, COA Profiles and Characteristics, and Raw Material Specifications.
Improves data structure quality and supply chain process efficiency by studying current practices and designing SAP data structure modifications or recommending network data alignment.
Support local/global SAP projects; participate in site user acceptance testing; provide user requirements review and input.
Proactively identify problems and own solutions for improving written procedures, business process instructions, workflows and training materials to maintain Operational Excellence.
Work independently on routine and non-routine production campaign-based activities; support team, department, site, and global project initiatives which impact the siteβs SAP Master Data structure; including product tech transfers under the direction of the manager or project lead.
Executes all work in accordance with Good Manufacturing Practice (GMP) standards, regulations, and documentation requirements.
Skills:
3+ years of GMP experience in a biotech, pharmaceutical, or chemical manufacturing environment.
5+ years of experience in creating/ maintaining SAP ECC master data.
Experience with use of computer-based systems, in a validated environment.
Able to organize large sets of electronic data in spreadsheets and databases.
Ability to influence both Supply Chain and functional leaders to support supply planning and site manufacturing strategy recommendations.
Good communication and presentation skills. Ability to present ideas in a clear and concise manner.
Strong analytical skills with the ability to support metrics (KPIβs) and identify issues through root cause analysis.
Competent using MS Office suite, particularly Excel and PowerPoint.
Ability to utilize Business Intelligence systems to extract data and generate reports.
Continuous improvement minded.
Job Title: ERP Business Analyst II
Location: Vacaville, CA (Hybrid Role)
Duration: 12 months + will be extended.
Work schedule: Mon - Fri, only 3 days in a week.
Job Summary:
The ERP Business Systems Analyst II is responsible for all SAP attributes of the site Product and Quality Master Data Management throughout the data lifecycle.
Manages master data changes in the ERP (SAP) System.
SME for training of stakeholders/staff on standard and best practices.
Duties:
Partners with internal and external stakeholders within Supply Chain, Manufacturing, Technology, Quality and Finance organizations to implement the production master data lifecycle in SAP (design, develop, deploy, maintain, optimize, audit, and retire).
Maintains a high-level understanding of the data related business processes and systems within/ outside the ERP system landscape to ensure SAP data domain compliance/ alignment.
Create, mature, maintain, and retire SAP Master Data Objects related to Production and Quality Data. This includes, but is not limited to Material Masters, Recipes, Bill of Materials, Resources, Master Inspection Characteristics, Info Records and ancillary support/ table data.
Create, mature, maintain, and retire SAP Master Data Objects related to Quality Management (QM) Data. Including Direct Material data, Inspection Plans, Sampling Schemes, Draw Procedures, COA Profiles and Characteristics, and Raw Material Specifications.
Improves data structure quality and supply chain process efficiency by studying current practices and designing SAP data structure modifications or recommending network data alignment.
Support local/global SAP projects; participate in site user acceptance testing; provide user requirements review and input.
Proactively identify problems and own solutions for improving written procedures, business process instructions, workflows and training materials to maintain Operational Excellence.
Work independently on routine and non-routine production campaign-based activities; support team, department, site, and global project initiatives which impact the siteβs SAP Master Data structure; including product tech transfers under the direction of the manager or project lead.
Executes all work in accordance with Good Manufacturing Practice (GMP) standards, regulations, and documentation requirements.
Skills:
3+ years of GMP experience in a biotech, pharmaceutical, or chemical manufacturing environment.
5+ years of experience in creating/ maintaining SAP ECC master data.
Experience with use of computer-based systems, in a validated environment.
Able to organize large sets of electronic data in spreadsheets and databases.
Ability to influence both Supply Chain and functional leaders to support supply planning and site manufacturing strategy recommendations.
Good communication and presentation skills. Ability to present ideas in a clear and concise manner.
Strong analytical skills with the ability to support metrics (KPIβs) and identify issues through root cause analysis.
Competent using MS Office suite, particularly Excel and PowerPoint.
Ability to utilize Business Intelligence systems to extract data and generate reports.
Continuous improvement minded.