At a Glance
- Tasks: Lead the NPI process for medical devices from concept to commercialisation.
- Company: Join a dynamic CDMO focused on innovative medical technologies.
- Benefits: Enjoy flexible working options and a collaborative team culture.
- Why this job: Be at the forefront of product innovation while making a real impact in healthcare.
- Qualifications: 3-5 years in project management within medical devices; degree in relevant field required.
- Other info: Experience with project management software is a plus; certification desirable.
The predicted salary is between 36000 - 60000 £ per year.
The New Product Introduction (NPI) Project Manager will lead the NPI process within a small but dynamic R&D department working on Medical Devices. As a member of a growing Contract Development and Manufacturing Organisation (CDMO), you will play a pivotal role in managing the introduction of new products and technologies from concept through to commercialisation. This includes overseeing project timelines, resources, budgets, and ensuring compliance with all regulatory requirements. The role will work closely with internal teams (R&D, Quality, Regulatory, and Manufacturing) as well as external clients, ensuring smooth execution of NPI projects while maintaining high standards of quality and customer satisfaction.
Key Responsibilities:
- Project Leadership and Management: Lead NPI projects by managing and coordinating all activities related to the introduction of new products, ensuring alignment with customer requirements, internal resources, and regulatory standards. Develop detailed project plans for each NPI, outlining scope, timelines, milestones, budgets, and risk management strategies. Ensure that key project milestones are met on time, within scope, and within budget while maintaining high-quality standards.
- Cross-Functional Collaboration: Collaborate with R&D and Engineering teams to ensure that product designs meet customer specifications and regulatory requirements and are manufacturable within the CDMO environment. Coordinate with Quality and Regulatory teams to ensure NPI projects comply with industry standards and regulations, including ISO 13485 and other relevant certifications. Work with Manufacturing to ensure a smooth handover from R&D to manufacturing, supporting scale-up activities and addressing any technical challenges in the transition to production.
- Client and Stakeholder Management: Act as the primary point of contact for clients, ensuring clear communication and alignment of project expectations, timelines, and outcomes. Provide regular updates to senior management, clients, and other stakeholders on project progress, potential delays, and mitigation strategies.
- Risk and Issue Management: Identify potential risks related to technical, regulatory, or operational challenges early in the process and develop strategies to mitigate them. Address issues that may arise during the NPI process, ensuring timely solutions are implemented to prevent delays or quality concerns.
- Compliance and Documentation: Ensure that NPI projects adhere to all relevant regulatory requirements, including those set by the MHRA, FDA, or other applicable bodies. Maintain accurate and detailed project documentation, including design history files, technical files, and change control records in line with industry standards.
- Continuous Improvement: Identify opportunities for improvement in the NPI process and work to implement best practices across future projects. Facilitate post-project reviews and capture lessons learned to improve efficiency and the quality of future NPI efforts.
- Resource and Budget Management: Manage and allocate resources (personnel, equipment, budget) effectively to ensure timely project execution. Monitor project costs and ensure that the project stays within the agreed budget, reporting any discrepancies or potential overruns to senior management.
Essential Attributes:
- Minimum of 3-5 years' experience in a project management role within a CDMO, medical device, or pharmaceutical industry.
- Proven experience managing NPI projects from concept to commercialisation, particularly within a regulated environment.
- Experience working with cross-functional teams in R&D, Quality, Regulatory, and Manufacturing departments.
- Strong project management skills, with experience in planning, execution, and delivery of projects within a set timeframe and budget.
- Knowledge of regulatory requirements for medical devices or pharmaceutical products (e.g., ISO 13485, GMP, FDA, etc.).
- Excellent communication, interpersonal, and organisational skills.
- Ability to manage multiple projects simultaneously and prioritise tasks effectively.
- Experience with project management software (e.g., MS Project, Jira, or similar tools).
- Strong problem-solving and analytical skills.
Qualifications / Certificates / Licenses:
- A degree in Engineering, Life Sciences, Chemistry, or a related discipline.
- A project management certification (e.g., PMP, Prince2) is highly desirable.
Desirable Attributes:
- Experience working in a small, fast-paced team environment across multiple disciplines.
- Knowledge of innovation management practices and IP.
- Familiarity with Lean or Six Sigma principles.
NPI Project Manager employer: Halian
Contact Detail:
Halian Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land NPI Project Manager
✨Tip Number 1
Familiarise yourself with the specific regulatory requirements for medical devices, such as ISO 13485 and FDA guidelines. This knowledge will not only help you in interviews but also demonstrate your commitment to compliance and quality standards.
✨Tip Number 2
Network with professionals in the CDMO and medical device sectors. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends and challenges in NPI project management.
✨Tip Number 3
Showcase your experience with project management software like MS Project or Jira during discussions. Being able to discuss how you've used these tools to manage timelines and resources effectively can set you apart from other candidates.
✨Tip Number 4
Prepare to discuss specific examples of how you've led cross-functional teams in past projects. Highlighting your ability to collaborate with R&D, Quality, and Manufacturing teams will demonstrate your fit for the role and your understanding of the NPI process.
We think you need these skills to ace NPI Project Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in project management, particularly within the medical device or pharmaceutical industry. Emphasise your skills in managing NPI projects and working with cross-functional teams.
Craft a Compelling Cover Letter: Write a cover letter that showcases your understanding of the NPI process and your ability to lead projects from concept to commercialisation. Mention specific examples of past projects where you successfully managed timelines, budgets, and compliance.
Highlight Regulatory Knowledge: In your application, emphasise your knowledge of regulatory requirements such as ISO 13485 and FDA standards. This is crucial for the role, so make sure to provide examples of how you've ensured compliance in previous projects.
Showcase Communication Skills: Since the role involves client and stakeholder management, highlight your communication and interpersonal skills. Provide examples of how you've effectively communicated project updates and managed expectations in past roles.
How to prepare for a job interview at Halian
✨Showcase Your Project Management Experience
Be prepared to discuss your previous experience managing NPI projects, particularly in a regulated environment. Highlight specific examples where you successfully led projects from concept to commercialisation, focusing on how you managed timelines, budgets, and compliance.
✨Demonstrate Cross-Functional Collaboration Skills
Since the role requires working closely with various teams, be ready to share examples of how you've effectively collaborated with R&D, Quality, Regulatory, and Manufacturing teams. Emphasise your ability to communicate clearly and align project expectations across different departments.
✨Understand Regulatory Requirements
Familiarise yourself with relevant regulatory standards such as ISO 13485 and FDA guidelines. During the interview, demonstrate your knowledge of these regulations and how you've ensured compliance in past projects, as this will be crucial for the role.
✨Prepare for Problem-Solving Scenarios
Expect questions that assess your problem-solving skills, especially regarding risk and issue management. Think of specific challenges you've faced in previous projects and how you addressed them, showcasing your analytical skills and ability to implement timely solutions.