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Job description

Leading Pharmaceutical Developer company seeks an experienced Project Coordinator

About the role:

To coordinate all aspects of customer projects through the entire life cycle of the project. To oversee a team of Project staff who are responsible for a portfolio of PDS projects.

Duties may include:

• Recruit, train and monitor performance of reporting staff, supporting, mentoring and coaching individuals to achieve highly effective levels of project management.
• Ensure customer specific requirements are met and communicated to all relevant disciplines.
• Ensure that all customer contact, oral and written is carried out professionally by reporting staff in order to develop and maintain good working relationships with each customer
• Monitor performance and workload within the reporting team and effect change where necessary to ensure each individual’s contribution to the project and customer is managed to the highest possible standard
• Maintain awareness of and as necessary, assist in the monitoring and control of client financial accounts.
• Track and report on both internal & customer metrics/KPIs
• Support Business Development and Quality by presenting at audits, customer meetings and workshops, as required.
• Coordinate and/or participate in project review meetings for key customers as necessary which may involve setting agendas and helping to prepare and deliver presentations.
• Deal with customer complaints escalated by reporting staff involving relevant Senior Managers as appropriate.
• Liaise with other departments to identify and improve cross-departmental processes and working relationships.
• Support cross-divisional initiatives pertaining to customer specific business projects and the key business area
• · Contribute to internal Projects where requested

Skills and experience:

• Bachelor’s degree (or equivalent) qualification
• Project Management with in the CMC/pharmaceutical area
• Manufacture of Clinical Supplies
• Formulation & Process Development
• Developing client accounts
• Proven ability to demonstrate knowledge of the regulatory framework governing development and commercialisation of pharmaceutical products
• Mentoring & coaching skills

Apply now for more information

Job Type: Permanent

Salary: £50,000.00-£65,000.00 per year

Schedule:

• 8 hour shift

Ability to commute/relocate:

• Loughborough: reliably commute or plan to relocate before starting work (required)

Education:

• Bachelor's (preferred)

Experience:

• Pharmaceutical Manufacturing: 3 years (preferred)
• GMP: 3 years (preferred)
• Process Development: 3 years (preferred)
• Project management: 1 year (preferred)

Work authorisation:

• United Kingdom (required)

Work Location: In person

Reference ID: MATECBB894