Location: Not Specified
_JOHNSON & JOHNSON WORKSENSE (VIA RANDSTAD SOURCERIGHT) IS RESPONSIBLE
FOR FINDING, ENGAGING AND CONTRACTING TALENT FOR THE JOHNSON & JOHNSON
CONTINGENT WORKFORCE._
We are currently seeking a PROJECT MANAGER to join our contingent
workforce at the Liffey Valley site in Dublin. The position will
initially be an **Apply on the website** months contract, with some
remote work available (there will also be onsite requirements).
The Project Manager will be support Johnson & Johnson&#**Apply on the
website**;s product and system transition from MDD to MDR. This
resource will lead Supply Chain-Deliver cutover plans and activities
across global and regional functional teams on the EU MDR and Version
Control Management implementation phase of the ongoing EU MDR project.
We are ideally seeking candidates with previous experience in med
device, or a highly compliance-driven / regulated environment.
THE ROLE:
As a Project Manager, you will lead the MDR implementation phase of
Johnson & Johnson&#**Apply on the website**;s EU MDR project, and
provide relevant assistance to a similar Version Control project. The
successful candidate will be tasked with:
PRODUCT TRANSITION MANAGEMENT FROM MDD TO MDR:
* Ensuring effective rolling change management through the MDD to
MDR transition, by working closely with the Network and Supply
Planning teams. Ensuring product is deployed to the right place at the
right time, in accordance with market registration constraints in a
controlled and compliant manner, whilst maintaining service
continuity.
* Responsibility for seamlessly transitioning supply planning to
down-stream supply chain organizations.
* Partnering with Supply chain workstream to execute cut over plans
* Ensuring phase planning is robust with full consideration for:
* Market registrations
* Product replacement / cannibalization
* MDR product phase-in, MDD product phase-out
* Define the key measures reports and KPIs for success
* Working with the MDR team to ensure a successful and controlled
product transition and discontinuation to MDD impacted products by
country of destination.
VERSION CONTROL MANAGEMENT - SYSTEMS AND TECHNICAL SUPPORT:
* Work with the Supply Chain functions to ensure systems parameters
are maintained in a timely manner through the full Product Life Cycle
of MDR related SKUs.
* Ensure process and systems are aligned to the MDR project to
support the Global Supply Chain deliver functions including key
deliverables:
* System control segregation
* Effective management and updates to rolling changes via accurate
reporting around timings and correct parameter setting to support
network planning and inventory deployment
* Ensuring accurate and timely reports are in place to correctly
identify and quantify with timings, potential risks in relation to
factors affecting service and cost.
MANAGING EU MDR ROLLOUT AND ENSURING EFFECTIVE SYSTEM CONTROLS ARE IN
PLACE TO SUPPORT PROPER EXECUTION.
SUPPORTING CAPACITY PLANNING & PROCESS MAPPING FOR CURRENT AND FUTURE
STATE AT EMEA DCS RELATIVE TO EU-MDR AND SKU LEVEL VERSION CONTROL
(MOD CODE) IMPLEMENTATION. Ensure E2E processes setup and system
controls are in place, starting from inbound receipts, order placement
& system allocations, pick & pack operations, returns, etc..
CANDIDATE REQUIREMENTS:
_EDUCATION:_
* B.S. degree in Engineering, Science, Supply Chain or equivalent
_PREVIOUS EXPERIENCE:_
* **Apply on the website** years of experience working in medical
device industry or equivalent (highly compliance-driven / regulated
environment), with a proven track record of successful project
management experience
* Experience / knowledge with EU MDR, labeling, supply chain highly
valuable
* Experience in working with multiple teams at different global
sites and complex systems
* Good knowledge of Supply Chain activities (demand, supply and
Inventory management), a good level of understanding of the Medical
Device Regulations and how they impact Supply Chain.
* Knowledge of SAP is highly valuable
* Well-versed in program and project management tools and practices,
including MS Project.
_OTHER RELEVANT SKILLS:_
* Excellent communication skills
* Ability to drive the projects without authorities
* Project Management skills
* Delivers on Commitments
* Product and market awareness, along with an understanding of
market dynamics and operations to apply that knowledge to the role.
* The ability to build Strong Relationships
* Cross Functional Collaboration skills
_IF YOU MEET OUR REQUIREMENTS AND ARE INTERESTED IN APPLYING FOR OUR
EU MDR PROJECT MANAGER ROLE, PLEASE DO NOT HESITATE TO APPLY THROUGH
THE PROVIDED LINK TODAY!_
Position: Project Manager (EU MDR)
Location: Not Specified
_JOHNSON & JOHNSON WORKSENSE (VIA RANDSTAD SOURCERIGHT) IS RESPONSIBLE
FOR FINDING, ENGAGING AND CONTRACTING TALENT FOR THE JOHNSON & JOHNSON
CONTINGENT WORKFORCE._
We are currently seeking a PROJECT MANAGER to join our contingent
workforce at the Liffey Valley site in Dublin. The position will
initially be an **Apply on the website** months contract, with some
remote work available (there will also be onsite requirements).
The Project Manager will be support Johnson & Johnson&#**Apply on the
website**;s product and system transition from MDD to MDR. This
resource will lead Supply Chain-Deliver cutover plans and activities
across global and regional functional teams on the EU MDR and Version
Control Management implementation phase of the ongoing EU MDR project.
We are ideally seeking candidates with previous experience in med
device, or a highly compliance-driven / regulated environment.
THE ROLE:
As a Project Manager, you will lead the MDR implementation phase of
Johnson & Johnson&#**Apply on the website**;s EU MDR project, and
provide relevant assistance to a similar Version Control project. The
successful candidate will be tasked with:
PRODUCT TRANSITION MANAGEMENT FROM MDD TO MDR:
* Ensuring effective rolling change management through the MDD to
MDR transition, by working closely with the Network and Supply
Planning teams. Ensuring product is deployed to the right place at the
right time, in accordance with market registration constraints in a
controlled and compliant manner, whilst maintaining service
continuity.
* Responsibility for seamlessly transitioning supply planning to
down-stream supply chain organizations.
* Partnering with Supply chain workstream to execute cut over plans
* Ensuring phase planning is robust with full consideration for:
* Market registrations
* Product replacement / cannibalization
* MDR product phase-in, MDD product phase-out
* Define the key measures reports and KPIs for success
* Working with the MDR team to ensure a successful and controlled
product transition and discontinuation to MDD impacted products by
country of destination.
VERSION CONTROL MANAGEMENT - SYSTEMS AND TECHNICAL SUPPORT:
* Work with the Supply Chain functions to ensure systems parameters
are maintained in a timely manner through the full Product Life Cycle
of MDR related SKUs.
* Ensure process and systems are aligned to the MDR project to
support the Global Supply Chain deliver functions including key
deliverables:
* System control segregation
* Effective management and updates to rolling changes via accurate
reporting around timings and correct parameter setting to support
network planning and inventory deployment
* Ensuring accurate and timely reports are in place to correctly
identify and quantify with timings, potential risks in relation to
factors affecting service and cost.
MANAGING EU MDR ROLLOUT AND ENSURING EFFECTIVE SYSTEM CONTROLS ARE IN
PLACE TO SUPPORT PROPER EXECUTION.
SUPPORTING CAPACITY PLANNING & PROCESS MAPPING FOR CURRENT AND FUTURE
STATE AT EMEA DCS RELATIVE TO EU-MDR AND SKU LEVEL VERSION CONTROL
(MOD CODE) IMPLEMENTATION. Ensure E2E processes setup and system
controls are in place, starting from inbound receipts, order placement
& system allocations, pick & pack operations, returns, etc..
CANDIDATE REQUIREMENTS:
_EDUCATION:_
* B.S. degree in Engineering, Science, Supply Chain or equivalent
_PREVIOUS EXPERIENCE:_
* **Apply on the website** years of experience working in medical
device industry or equivalent (highly compliance-driven / regulated
environment), with a proven track record of successful project
management experience
* Experience / knowledge with EU MDR, labeling, supply chain highly
valuable
* Experience in working with multiple teams at different global
sites and complex systems
* Good knowledge of Supply Chain activities (demand, supply and
Inventory management), a good level of understanding of the Medical
Device Regulations and how they impact Supply Chain.
* Knowledge of SAP is highly valuable
* Well-versed in program and project management tools and practices,
including MS Project.
_OTHER RELEVANT SKILLS:_
* Excellent communication skills
* Ability to drive the projects without authorities
* Project Management skills
* Delivers on Commitments
* Product and market awareness, along with an understanding of
market dynamics and operations to apply that knowledge to the role.
* The ability to build Strong Relationships
* Cross Functional Collaboration skills
_IF YOU MEET OUR REQUIREMENTS AND ARE INTERESTED IN APPLYING FOR OUR
EU MDR PROJECT MANAGER ROLE, PLEASE DO NOT HESITATE TO APPLY THROUGH
THE PROVIDED LINK TODAY!_
We need : English (Good)
Type: Permanent
Payment:
Category: Others
