Technical Project Manager

Proclinical; Taunton; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading life sciences recruiter is seeking a Technical Project Manager to oversee medical device development from concept to commercialization in Taunton, UK. This role involves ensuring compliance with quality and regulatory standards, developing project plans, and leading cross-functional teams. Ideal candidates will have strong project management principles, experience in budgeting, and technical knowledge in engineering or science. This is an exciting opportunity to drive innovation in the medical device industry.

Qualifications

• Strong understanding of project management principles and tools.
• Experience in budgeting and resource allocation for technical projects.
• Familiarity with product development lifecycles in regulated industries.

Responsibilities

• Develop and maintain detailed project plans and milestones.
• Utilize project management tools to track progress.
• Communicate effectively with project teams and stakeholders.

Skills

Project management principles

Budgeting and cost control

Analytical skills

Risk management

Leadership

Communication

Stakeholder engagement

Education

Formal project management qualification (PMP, PRINCE2)

Technical foundation in engineering or science

Tools

Smartsheet

MS Project

Excel

PowerPoint

Word

Teams

Outlook

Job description

Lead breakthrough medical device innovations from concept to commercialization with precision, purpose, and cross‑functional excellence.

Proclinical is seeking a Technical Project Manager to lead innovative medical device development projects from concept to commercialization. This role focuses on disciplined project execution, ensuring alignment with business objectives and compliance with quality and regulatory standards. You will work in a collaborative environment, driving project success through effective planning, communication, and stakeholder engagement.

Responsibilities

• Develop and maintain detailed project plans, ensuring timely achievement of milestones.
• Utilize project management tools like Gantt charts and software (e.g., Smartsheet, MS Project) to track progress and dependencies.
• Communicate effectively with project teams, stakeholders, and leadership, providing clear updates and facilitating decision‑making.
• Identify, assess, and mitigate project risks while managing budgets and expenditures (OPEX/CAPEX).
• Ensure compliance with medical device quality and regulatory requirements (e.g., ISO 13485) and internal Quality Management System procedures.
• Support continuous improvement initiatives, including lessons learned workshops and process enhancements.
• Build and lead cross‑functional project teams, fostering collaboration and alignment with business goals.

Key Skills and Requirements

• Strong understanding of project management principles, methodologies, and tools.
• Experience in budgeting, cost control, and resource allocation for technical projects.
• Technical foundation in engineering or science with analytical skills and the ability to grasp new concepts.
• Familiarity with product development lifecycles, particularly in regulated industries like medical devices.
• Knowledge of quality management systems, risk management, and good documentation practices.
• Proficiency in project management software (e.g., Smartsheet, MS Project) and office productivity tools (Excel, PowerPoint, Word, Teams, Outlook).
• Strong leadership, communication, and stakeholder engagement skills.
• Ability to manage competing priorities, mitigate risks, and resolve complex project issues.
• Formal project management qualification (e.g., PMP, PRINCE2) and experience with Agile or Scrum methodologies are advantageous.

Nathan Berkley at [e-mail]

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