Pharmaceutical Project Manager

Posted 21 days ago by Pertemps
Location Wiltshire Job Type Temporary
Salary £25.00 - £30.21 per hour, Benefits: Free- Parking Onsite Sector HSE, Security & Risk Management, Health & Medical, Education & Training, Professional & Admin, Manufacturing & Industrial, Executive and Management, Engineering
Pertemps would like to present you with an exciting Opportunity based in Wiltshire!!  Are you an experienced Project Manager??? We need a Pharmaceutical Project Manager on a 12 Month Temporary Assignment.

We are looking for a full-time , experienced  Project Manager from a Pharmaceutical cGMP/Scientific or GMP Manufacturing background.
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 Manufacturing background.

Salary: between £25.00 per hour to £30.21 Depending on experience.

Working Hours: 35 per week 

Fantastic Benefits with an amazing company

Location: Wiltshire

The Technical 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 GMP manufacturing 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 manufacturing experience
BS degree in Electrical/ Mechanical/ Chemical Engineering preferred, or equivalent years of experience.

Strong organisational and teamwork skills.
Ability to influence and manage individuals without having direct authority over those individuals.
Effective oral, written, and interpersonal English communication skills, including presentation skills.
Creative problem solver with ability to work effectively, both independently and as an integral contributor on a multi-disciplinary team.
Budget, Forecasting, and understanding of actual business events and related financial implications.
Proficient at creating and managing detailed Excel spreadsheets and Microsoft Project Plans.
Knowledge of cGMP, aseptic processes, and/or automated systems is a plus.
Have a sense of urgency and ownership to meet company and project time-lines and objectives.

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 ASAP or better still send us your CV ASAP. 

We are here to help!!!!  give us a Call or Knock our door!!