At a Glance
- Tasks: Lead and coordinate the development of complex medical devices and ensure project success.
- Company: Cirtec Medical is a top partner in medical device outsourcing, focusing on innovation and collaboration.
- Benefits: Enjoy competitive pay, healthcare, career development, and a supportive work environment.
- Why this job: Join a culture of growth and innovation while making a real impact in healthcare.
- Qualifications: Bachelor's degree and 5 years in project management; PMP certification preferred.
- Other info: This role requires onsite presence and offers opportunities for travel.
The predicted salary is between 80000 - 120000 £ per year.
About us: For over three decades, Cirtec Medical has been a leading outsourcing partner for complex medical devices. We specialize in providing comprehensive solutions for Class II and III devices, from design and development to precision components and finished device assembly. Our expertise spans neuromodulation, implantable drug delivery, cardiac rhythm management, structural heart, mechanical circulatory support, and minimally invasive surgical systems. Our dedicated teams prioritize growth, innovation, and collaboration. We actively seek opportunities for improvement to enhance our support for clients. If you embrace a growth mindset and thrive on challenges, you may be a perfect fit for our team! Position Summary: The Sr. Project Manager position is primarily responsible for managing and coordinating development and manufacturing transfer of complex components and finished medical devices. Key Responsibilities: Manages and coordinates development and manufacturing transfer of complex components, sub-assemblies and finished medical devices. Generates and maintains detailed project plans, task lists and project risk registers that enable the team to execute project activities based on well-defined prioritization. Coordinates activities across different functional groups to ensure successful completion of project goals and milestones. Tracks project health in terms of schedule, budget, and technical risks and issues. Prepares and presents comprehensive project status reports to internal and external stakeholders Proactively anticipates project risks and issues, and carefully formulates and implements risk mitigations and corrective/preventive actions Creates and maintains Design History file per internal company procedures, FDA Design Control (21 CFR 820) and ISO 13485 requirements Supports project team in establishing and maintaining product requirements and test plans Serves as the principal contact with external customers. Coordinates and directs customer meetings and visits, and day-to-day customer communication. Manages internal resource allocation to meet program goals and milestones. Works with internal management to ensure appropriate resources have been assigned. Reliable, consistent, and punctual attendance is an essential function of the job Oversees complex or multiple projects, ensuring alignment with business goals. Manage higher-risk initiatives, mentor junior project managers, and collaborate with senior leadership to optimize processes, budgets, and resources. This is not a remote position. Must Have: Bachelor\’s degree in business, engineering, IT, or related field. PMP certification preferred. Minimum 5 years of experience in project / program management of medical device development Experience with metals processing and Nitinol-based devices preferred but not required Must possess strong understanding and working knowledge of ISO 13485 and FDA 21CFR820 based Quality Systems and Design Control Must be able to interpret technical drawings, product requirements, design specifications and relevant technical documents Ability to condense and communicate complex technical ideas, project status and risks to internal and external stakeholders Must have proficiency in MS Project and other MS Office software Must be able to read, write and speak fluent English, and must possess excellent communication skills, both written and oral Willingness to travel, if required Salary Range: $115-125K Dependent upon experience Cirtec Medical Corporation considers for employment and hires qualified candidates without regard to age, race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, protected veteran or disability status or any factor prohibited by law. Cirtec Medical Corporation and all of its related companies fully endorse equal opportunity for all. Cirtec Medical provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in the job application process. We work to create a culture that is built on innovation, respect, transparency and communication, and hope you take pride in being a member of our team. It is Cirtec\’s goal to create a great work environment and to keep the company a great place to work. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Our benefits include Training and career development, Healthcare and well-being programs including medical, dental, vision, wellness and occupational health programs, Paid Time Off and 401(k) retirement savings with a company match. #J-18808-Ljbffr
Sr. Project Manager employer: Cirtec Medical
Contact Detail:
Cirtec Medical Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Sr. Project Manager
✨Tip Number 1
Familiarise yourself with the specific medical device regulations, particularly ISO 13485 and FDA 21 CFR 820. Understanding these standards will not only help you in interviews but also demonstrate your commitment to quality and compliance in project management.
✨Tip Number 2
Highlight your experience in managing complex projects, especially in the medical device sector. Be prepared to discuss specific examples where you've successfully coordinated cross-functional teams and navigated challenges, as this aligns closely with the responsibilities of the Sr. Project Manager role.
✨Tip Number 3
Showcase your proficiency in MS Project and other MS Office tools. Being able to effectively manage project plans and communicate status updates is crucial for this position, so consider preparing a brief demonstration of your skills if the opportunity arises during the interview.
✨Tip Number 4
Prepare to discuss your approach to risk management in projects. Given the emphasis on anticipating project risks and implementing mitigations, having a clear strategy or framework that you can share will set you apart as a candidate who is proactive and solution-oriented.
We think you need these skills to ace Sr. Project Manager
Some tips for your application 🫡
Tailor Your CV: Make sure to customise your CV to highlight relevant experience in project management, particularly in the medical device sector. Emphasise your familiarity with ISO 13485 and FDA regulations, as well as any specific projects that align with Cirtec Medical's focus.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for the medical device industry and your growth mindset. Mention specific examples of how you've successfully managed complex projects and how you can contribute to Cirtec Medical's goals.
Highlight Key Skills: In your application, clearly outline your proficiency in MS Project and other MS Office software. Also, demonstrate your ability to communicate complex technical ideas effectively, as this is crucial for the Sr. Project Manager role.
Showcase Leadership Experience: If you have experience mentoring junior project managers or leading teams, make sure to include this in your application. Cirtec Medical values collaboration and leadership, so highlighting these experiences will strengthen your application.
How to prepare for a job interview at Cirtec Medical
✨Understand the Company and Its Products
Before your interview, take some time to research Cirtec Medical and its range of medical devices. Familiarise yourself with their focus areas like neuromodulation and implantable drug delivery. This knowledge will help you demonstrate your genuine interest in the company and its mission.
✨Showcase Your Project Management Skills
Be prepared to discuss your previous project management experiences, especially in the medical device sector. Highlight specific projects where you managed complex components or led cross-functional teams. Use the STAR method (Situation, Task, Action, Result) to structure your responses.
✨Emphasise Risk Management Experience
Given the importance of risk management in this role, be ready to share examples of how you've proactively identified and mitigated risks in past projects. Discuss any tools or methodologies you used to track project health and ensure successful outcomes.
✨Prepare for Technical Questions
Since the role requires a strong understanding of ISO 13485 and FDA regulations, brush up on these standards. Be ready to explain how you've applied them in your previous roles, and be prepared to interpret technical documents or drawings if asked.