pharmaceutical or biotech industry and will have demonstrated project
management skills?
This is a contract role based in Dublin.
If you have the relevant experience, please forward your CV to **Apply
on the website** for review or call * **Apply
on the website** to discuss in confidence.
SENIOR PROJECT MANAGER – BIOTECH PROCESS DEVELOPMENT - DUBLIN
JOB DESCRIPTION
Our client is a leading international Biotechnology company with a
state of the art aseptic manufacturing facility in Dun Laoighaire,
South Dublin.
The plant is one of the most dynamic in Ireland and is currently
undergoing rapid expansion and capital investment.
This is an excellent opportunity to get experience on Ireland&#**Apply
on the website**;s leading aseptic manufacturing plant.
The Project Manager – Process Development will report to the Sr.
Manager Process Development in the Portfolio Management and Delivery
(PMD) group and will be responsible for managing new product
introduction and lifecycle management projects for drug product (DP)
and finished drug products (FDP).
Experience in a leadership role in a pharmaceutical or biotech
manufacturing facility that engages with site SMEs and managers, and
global functions
The ability to influence and lead cross functional teams to deliver to
ensure the smooth introduction of new products and the health of
existing products
The ability to work independently and identify risks and mitigation
pathways for new and existing products
A passion for continuous improvement applied to product and program
leadership
Arrange agreement among the project team, customers, and management on
the goals of the project
Develops and maintains the Project schedule/plan that addresses
quality, objective, scope, cost, schedule, resources, and
responsibilities - to deliver the project, and measure progress
against schedule and budget
Effectively communicate with everyone involved in the project
Have a controlled scope in place, that is understood by all
stakeholders and maintained throughout completion of the project
Execute prudent risk and issue management.
Maintains Actions/Risk and Decision logs
Generates and owns the GMP change control.
Motivate, support and direct project team members to deliver on
project plan.
Leads Team meetings and cross functional collaboration
Works with resource managers from across the organisation to
effectively obtain and allocate resources to complete programs and
projects on time
Compliance Related Tasks
Always ensure compliance to cGMP
Ensure safety & compliance standards are maintained to the highest
standards
Ensure financial compliance in line with Business & Financial guidance
Support a culture of personal responsibility within reporting
structure
REQUIREMENTS
Technical Degree and/or Masters’ or equivalent
* years of experience (including min of 3yrs as
Project Manager) in a Life Science / Pharmaceutical / Biotechnology
Environment
Preferred Experience: Portfolio Management, Portfolio Resource
Management, Business Case Development
MS Office, MS Project, MS PowerPoint and MS Visio,
Change Control & Document Management Systems
Preferred Requirements: Smartsheet
High Energy and Commitment
Ability to work independently
Comfortable leading across multiple stakeholders & multinational teams
Strong ability to influence and affect change
Capable of resolving issues of conflict effectively
Strong communicator
A proven track record in the ability to transfer goals and objectives
into measurable plans
Ability to identify gaps/risks and put appropriate remediation plans
in place
Uses strong relationships to identify requirements and potential
opportunities
Employs project management techniques and Problem Solving
Provides leadership, guidance, and advice in own field of project
management
PACKAGE
Contract role
Hourly Rate € * - € *
per hour
Minimum * month contract
We need : English (Good)
Type: Permanent
Payment: EUR 55 - 65 Per Hour
Category: Construction
