
Bristol Myers Squibb
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more careers.bms.com/working-with-us.
In this position the OSD Manufacturing Master Data – Specialist will execute tasks related to Manufacturing and Quality Control master data in the Manufacturing ERP System (SAP) following the GXP guidelines.
This includes and is not limited to data entry, data analysis, workflow follow-up, functional testing of ERP system, manufacturing ERP data technical development, master data SME, and coordinate or lead on manufacturing ERP data project.
This position will work in close collaboration with Boudry Manufacturing departments, Global Master Data, Quality Assurance and other internal stakeholders.
Duties/Responsibilities
The OSD Manufacturing Master Data – Specialist
- Is able to timely execute the assigned tasks and assess the impact of these changes upon other Manufacturing ERP Data within the ERP system. He/She understands the full scope and is consulted during the reflection on timelines and impacts.
- Prepares and follows data templates and workflows in order to meet the requested timelines and makes the data entry in the ERP system.
- Is CAPA action owner and change control action owner and must ensure that the proper actions are done in due time and according to the GxP guidelines and liaise with more global project timelines.
- Collects user’s requests and proactively proposes solutions for improvement to the impacted departments and involve the relevant person upon need. He/She will creatively think of solution that could be process oriented.
- Coordinates the stakeholder session of routing improvement.
- Analyse the impact of improvement request and will advise the stakeholder of the impact and will take the relevant action in order to stay aligned across routings with timelines
- Ensures proper IT development; implements and executes the needed data tests/loads within the ERP system.
- Has the expertise to conceptualize, create and update packaging routings and to update existing bulk routings.
- Provides necessary training on routings and other master data for any employee, function or department requiring such training.
- Plays an active role during UAT sessions for ERP improvement or org developments. He/she can be consulted during UAT script creation, execution of tests related to master data, production, QC, QA, Scheduling and Warehouse functions/modules, and can also participate as coordinator for these sessions.
- Is expert in using the different tool related to data entry, such as data loader and/or conversion tool.
- Participates to data collection for KPI analyses and KPI set-ups.
- Participates in project related to MDM activities as subject master expert and can lead or co-lead such projects.
- Act as the back-up of his/her peers and managers mainly regarding coordination activities.
Qualifications
- Commercial diploma, (CFC ) or equivalent
- at least 2 year’s of experience in Manufacturing Master Data management ( Materiel Master, BOM, and Receipe) ( mandatory)
- Conscientious, reliable in action follow-up and priority management
- Strong team-player
- Fluency both in French and English is required
- Good insight in processes and dependencies
- Concentrated conscious, aiming for “right first time”
- Aiming for the full picture and the full understanding of the of other’s implication
- Interested and skills in relationship and cross-department interactions.
- Strictly follow established processes but also be able to actively contribute in defining new processes
- Interested and motivated to expand project lead skills
- A first experience with manufacturing ERP
- Excellent IT proficiency MS Office, Excel, SAP
- GxP mindset and culture
- First experiences in project management is an asset.
If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
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