At a Glance
- Tasks: Lead and manage multiple high-impact projects in a dynamic healthcare environment.
- Company: Join a leading global healthcare and medical device manufacturer.
- Benefits: Competitive salary up to £80,000, with opportunities for contract extension or permanent role.
- Other info: Fast-paced environment with strong potential for professional growth.
- Why this job: Make a real difference in healthcare while advancing your project management career.
- Qualifications: Experience in managing technical projects in regulated environments; project management certification preferred.
The predicted salary is between 80000 - 80000 £ per year.
Location: Witney, UK (Full-Time, On-Site)
Contract Length: 12 Months (Initial contract with a strong view to extend or convert to permanent)
Salary/Rate: Up to £80,000 per annum (Depending on experience)
About the Role
We are seeking a dynamic and highly organized Project Manager to join a leading global healthcare and medical device manufacturer at their facility in Witney. In this role, you will sit at the intersection of innovation and compliance, orchestrating multiple concurrent projects across three critical pillars: Quality Assurance (QA), Manufacturing Execution Systems (MES), and Validation. This is an exceptional opportunity to manage high-impact projects within a matrixed global entity. Whether you are an experienced PM looking for a complex new challenge, or a structured scientific professional eager to transition into full-time project management, this role offers a clear path for professional growth.
Key Responsibilities
- End-to-End Delivery: Plan, execute, and deliver multiple complex projects simultaneously within QA, Validation, and MES frameworks.
- Cross-Functional Collaboration: Act as the primary bridge between engineering, IT/systems, quality assurance, and laboratory teams to ensure seamless project execution.
- Timeline & Budget Management: Develop detailed project plans, define milestones, manage resource allocation, and track budgets up to successful closure.
- Risk & Compliance: Ensure all projects strictly adhere to global regulatory standards (e.g., FDA, ISO 13485, GMP). Identify potential bottlenecks early and implement mitigation strategies.
- Stakeholder Communication: Provide clear, concise progress reports and presentations to local leadership and global stakeholders.
What We Are Looking For
- Proven track record of managing multiple technical projects within a Pharmaceutical, Medical Device, or highly regulated manufacturing environment.
- Strong working knowledge of Validation protocols (IQ/OQ/PQ), QA processes, or the implementation/upgrade of MES (Manufacturing Execution Systems).
- Formal project management certification (e.g., PRINCE2, PMP, or Agile) is highly desirable.
Personal Attributes
- Resilient & Adaptable: Thrives in a fast-paced, evolving manufacturing environment.
- Strong Communicator: Ability to influence and build relationships with technical experts and senior business leaders alike.
- Problem Solver: Analytical mindset with a proactive "can-do" attitude toward overcoming project roadblocks.
Senior Project Management Coordinator in Witney employer: Randstad
Join a leading global healthcare and medical device manufacturer in Witney, where innovation meets compliance in a collaborative and dynamic work environment. With a strong focus on employee growth, this role offers a clear pathway for professional development, competitive salary, and the opportunity to manage impactful projects that contribute to global health standards. Experience a supportive culture that values resilience, adaptability, and effective communication, making it an excellent place for ambitious professionals seeking meaningful and rewarding employment.
