|Salary||£25.00 - £30.21 per hour, Benefits: Free- Parking Onsite||Sector||HSE, Security & Risk Management, Health & Medical, Government & Public Sector, Education & Training, Professional & Admin, Manufacturing & Industrial, Executive and Management, Engineering|
We are looking for a full-time , experienced Project Manager from a Pharmaceutical cGMP/Scientific or Medical background and If you have a Prince2 this is a huge bonus!!
The role is a Pharmaceutical Project Manager , this is not a software or IT Project Manager role we need an experienced Project Manager from the Pharmaceutical or Medical /Science background.
This Pharmaceutical Project Manager role requires at least 5 years plus experience.
Salary: between £25.00-£30.21 per hour depending on experience.
Working Hours: 35 per week
Fantastic Benefits with an amazing company
The Pharmaceutical or Scientific Project Manager will be responsible for managing the qualification and commercial launch of new manufacturing line located in Wiltshire. The project scope includes a new manufacturing line, waste abatement equipment, and the technical transfer of quality methods from the contract manufacturing vendor (CMO). The anticipated duration of the project is 12 months, from commissioning of equipment to regulatory approval. The Project Manager will work with all functions of the company's technical operations and the CMO in support of key project deliver-ables. The Technical Project Manager, working closely with the CMO's Project Manager, is responsible for facilitating cross-functional team coordination through the project management life cycle, including project initiation, planning, execution, performance control, and reporting. Knowledge of cGMPs and experience with Medical/Scientific/Pharmaceutical is essential.
Facilitate overall project coordination, execution, communication, and discussions between client and the CMO. Document work breakdown structure and related deliver-ables in project planning tools.
Create the appropriate resource and execution plan, including defined roles and responsibilities, to achieve milestones.Coordinate, verify, and track Commissioning and Installation-Operational Qualification (IQQ) protocols for pharmaceutical systems and equipment. Monitor Training status and GMP document generation (SOP's and BR's) Project Change Control tracking. Track validation plans and document approval. Raw material and process development batch forecasting Scheduling Plant Maintenance and Shutdown activities into overall project schedule. Managing capital expenditure and expense budgeting, including purchase order and invoice management.Ensuring timely service, quality, and accountability from the CMO.Effectively identify, communicate, and manage risks associated with project execution.
Ability to communicate overall project status, schedule, budget adherence, and risks to project team, sponsor, stakeholders, and steering committee. The ability to understand and work across many functional disciplines; and act as a key liaison with the CMO.
Education/Experience required for this role:
Direct experience with Project Management, PMBOK guidelines and standards. PMP Certification not required, but preferable.
Relevant cGMP Pharmaceutical /Medical /Pharmaceutical Manufacturing experience
BS degree in Electrical/ Mechanical/ Chemical Engineering preferred, or equivalent years of experience.
We would certainly like to hear from you if you have the above proven experience, you want a fresh start ! A great employer, amazing company in Wiltshire then please call Pertemps Chippenham Branch 01249 467665 ASAP or better still send us your CV ASAP.