Jobs in Tredegar, gwent, uk

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

We are looking for a Director of Pharmaceutical Development to join our team in Tredegar, Wales.

Main purpose of role :

To lead and inspire the Pharmaceutical Development groups, to deliver technical excellence and agreed client development milestones. To support Development & Manufacturing thought leadership efforts, PCI BD sales support, and strong leadership, developing a team of experts at the Tredegar site to drive an ecosystem of strong science and customer service.

Main responsibilities :

• Responsible for the leadership and strategy of the Pharmaceutical Development groups within PCI Pharma Services, Tredegar.
• Responsible for provision of technical excellence for development projects (solid oral, liquids and semi solids), in line with industry expectations.
• To efficiently deliver the client project portfolio of the Pharmaceutical Development Department to agreed project milestones.
• Responsible for delivering Pharmaceutical Development revenue.
• To provide technical support for Business Development in relation to client meetings, teleconferences and technical scopes for projects and proposals.
• To act as a source of Technical Expertise within the company, keeping abreast of developments within the field by attendance of technical seminars / conferences, Linkedin learning and scientific papers.
• To work with the GM and the Continuous Improvement Manager to achieve continuous improvements site targets, and continuous improvement mindset within development groups.
• To ensure all staff achieve the agreed quality compliance targets for the site, supporting client and regulatory audits as required.
• To be responsible for the selection, training and development, quarterly reviews and performance of development staff.
• Ensure that all staff within the area of responsibility comply with PCI Pharma services Environmental Health and Safety Policies and Procedures.
• To ensure additional client scope of work activities are captured appropriately, to achieve agreed monthly revenue targets
• To manage the budgets of the department.
• Member of the Site Leadership Team.
• Authority for expenditure as defined in the purchasing authority levels document
• To identify self-development needs in conjunction with the General Manager.
• To undertake such tasks and to manage specific internal or ad hoc projects as and when required to meet department and business needs and within the scope of the job-holder’s capabilities and responsibilities.

Regulatory / Industry Responsibilities :

General

GMP Requirements Hierarchy

further information regarding GMP Requirements Hierarchy, can be obtained at SOP-L&D-001)

Qualifications :

Experience :

QUALIFICATIONS & TRAINING :

Scientific degree e.g. Chemistry and / or related scientific discipline or equivalent industry experience

KNOWLEDGE :

Expert in Pharmaceutical Development, Clinical manufacture, process scale up and validation.

Extensive knowledge in the fields of process technology and / or pharmaceutical development, ideally in potent OSD.

EXPERIENCE :

Extensive Industry experience

SKILLS & APTITUDES :

Excellent written and verbal communication skills.

Ability to operate at a senior level and work to deliver to tight timelines

PERSONAL QUALITIES AND BEHAVIOURS :

Highly driven and Passionate

Growth Mind-set

Self Confidence

Resilience

Customer focussed

OTHER REQUIREMENTS

Green Belt Certified

Join us and be part of building the bridge between life changing therapies and patients.