Pharma Project Manager — Client-Facing, GMP & Delivery

SRG; Falkirk; Hybrid; GBP 45,000 - 65,000; Full time

Job summary

SRG is seeking a confident Project Manager to lead complex, high-value programmes in Grangemouth. You will liaise with Business Development, R&D, Operations, Quality and Finance to shape and deliver projects on time, on budget and to a high standard.

The role requires a scientific degree, pharma industry experience, and a strong grounding in cGMP. After probation, the role is hybrid with management approval.

Qualifications

• Bachelor's degree in a scientific discipline.
• Experience in the pharmaceutical/life sciences industry.
• PMP certification is a strong advantage.
• Solid grounding in cGMP and commercial project delivery.
• Excellent communication skills to engage stakeholders at all levels.
• Strong organisational skills to manage multiple live projects.
• Self-starting and enthusiastic approach to driving opportunities

Responsibilities

• Managing multiple concurrent projects with scope, timelines and financial milestones.
• Acting as the primary client contact, communicating on quality, budget and delivery.
• Building and maintaining project plans and RAID logs as standard practice.
• Spotting risk and scope creep early and leading mitigation discussions.
• Tracking revenue forecasts and reporting milestones to Finance.
• Chairing team meetings and ensuring effective information flow.
• Mentoring colleagues to foster a high-performing team culture

Skills

Project management

Stakeholder engagement

Client-facing communication

Organisational skills

Mentoring

Proactive/self-starting

Education

Bachelor's degree in a scientific discipline

PMP certification (advantage)

Job description

SRG is seeking a confident Project Manager to lead complex, high-value programmes in Grangemouth. You will liaise with Business Development, R&D, Operations, Quality and Finance to shape and deliver projects on time, on budget and to a high standard.

The role requires a scientific degree, pharma industry experience, and a strong grounding in cGMP. After probation, the role is hybrid with management approval.